FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Kanjaksha Ghosh

Research Profile

Geographic Areas

India

Disorders

Chemicals & Drugs

Physiology

Concepts & Ideas

Living Beings

Procedures

Genes & Molecular Sequences

Alleles

Co-author Network

Publications

TOP 3
Kanjaksha Ghosh
Multifactorial aetiology for bone disease in patients with haemophilia.
Prashant Warang; Kanjaksha Ghosh; Rakhee Kar; Prabhakar Kedar; Roshan B Colah
New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia.
Vandana D Pradhan; Anjali Rajadhyaksha; Vinod Rajendran; Prathamesh Surve; Shruti Dighe; Gauri Mahant; Anita Nadkarni; Manisha Patwardhan; Kanjaksha Ghosh
A study on anti-mannose binding lectin (anti-MBL) antibodies and serum MBL levels in Indian systemic lupus erythematosus patients.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Kanjaksha Ghosh (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Kanjaksha Ghosh
Multifactorial aetiology for bone disease in patients with haemophilia.
European journal of haematology 2013;90(5):435.
2013: Prashant Warang; Kanjaksha Ghosh; Rakhee Kar; Prabhakar Kedar; Roshan B Colah
New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia.
Annals of hematology 2013;92(5):715-7.
2013: Vandana D Pradhan; Anjali Rajadhyaksha; Vinod Rajendran; Prathamesh Surve; Shruti Dighe; Gauri Mahant; Anita Nadkarni; Manisha Patwardhan; Kanjaksha Ghosh
A study on anti-mannose binding lectin (anti-MBL) antibodies and serum MBL levels in Indian systemic lupus erythematosus patients.
Rheumatology international 2013;33(5):1193-9.
2013: Pallavi Shukla; Kanjaksha Ghosh; Anita Rao; Babu Rao Vundinti
Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature.
Gene 2013;518(2):470-5.
2013: Vandana D Pradhan; A Rajadhyaksha; M Patwardhan; Kanjaksha Ghosh
Clinical and immunological profile of systemic lupus erythematosus.
Indian pediatrics 2013;50(4):405-7.
2013: Manisha Madkaikar; Snehal Mhatre; Anju Mishra; Mukesh Desai; Maya Gupta; Kanjaksha Ghosh
Comprehensive report of primary immunodeficiency disorders from a tertiary care center in India.
Journal of clinical immunology 2013;33(3):507-12.
2013: Devaraj Jatteppa Parasannanavar; Vandana Pradhan; Anjali Rajyadhaksha; Avani Yeola; Kanjaksha Ghosh
HLA-DRβ1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients.
Rheumatology international 2013;33(4):867-70.
2013: Kanjaksha Ghosh
Cytogenetics in paediatric aplastic anaemia: Does it give an insight on the evolution of the disease?
The Indian journal of medical research 2013;137(3):445-6.
2013: Pooja Dabke; Kanjaksha Ghosh; Roshan B Colah; Anita H Nadkarni
Effect of a group of genetic markers around the 5' regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia.
Blood cells, molecules & diseases 2013;50(3):156-60.
2013: Aude Magerus-Chatinet; Bénédicte Neven; Nathalie Neveux; Capucine Picard; Meghana Rao; Cécile Daussy; Mukesh Desai; Alain Fischer; Kanjaksha Ghosh; Nina Lanzarotti; Manisha Madkaikar; Marie-Claude Stolzenberg; Frédéric Rieux-Laucat
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation.
The Journal of allergy and clinical immunology 2013;131(2):486-90.
2013: Tejasvita Gaikwad; Kanjaksha Ghosh; Shrimati Shetty
Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy.
European journal of clinical pharmacology 2013;69(2):293-4.
2013: Selma D'Silva; Kanjaksha Ghosh; Roshan B Colah; Malay B Mukherjee
UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.
Gene 2013;513(1):36-9.
2013: E D'Souza; Kanjaksha Ghosh; Ajit C Gorakshakar; A H Nadkarni; P M Sawant; Roshan B Colah
Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma.
Journal of postgraduate medicine 2013;59(1):15-20.
2013: Sona B Nair; Kanjaksha Ghosh; Anita H Nadkarni; Roshan B Colah
Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T(Indian) (AATAAA>AATA- -) Mutation in Four Indian Families.
Hemoglobin 2013;37(3):277-84.
2013: Pooja Dabke; Kanjaksha Ghosh; Roshan Colah; Anita H Nadkarni
Effect of Cis Acting Potential Regulators in the β Globin Gene Cluster on the Production of HbF in Thalassemia Patients.
Mediterranean journal of hematology and infectious diseases 2013;5(1):e2013012.
2013: Anita Patil; Bishesh Sharma Poudyal; Kanjaksha Ghosh; Sanu Maiya Kapali; Shrimati Shetty
Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
Annals of hematology 2013;92(2):261-2.
2013: Swati Kulkarni; Vasantha Kasiviswanathan; Kanjaksha Ghosh
A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.
Blood transfusion = Trasfusione del sangue 2013;11(1):37-42.
2012: Prabhakar Kedar; Prashant Warang; Kanjaksha Ghosh; Roshan B Colah
Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family.
Annals of hematology 2012;91(12):1985-6.
2012: Manisha Rajan Madkaikar; Meghana Rao; Maya Gupta; Kanjaksha Ghosh
Prenatal diagnosis of LAD-I on cord blood by flowcytometry.
Indian journal of pediatrics 2012;79(12):1605-9.
2012: Shirimati Shetty; Kanjaksha Ghosh
APTT reagents for different coagulation tests: one size does not fit all.
American journal of clinical pathology 2012;138(5):757; author reply 757-8.
2012: Anshul Jadli; Bipin Kulkarni; Kanjaksha Ghosh; Shrimati Shetty
Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases.
Liver international : official journal of the International Association for the Study of the Liver 2012;32(10):1596-7.
2012: Kanjaksha Ghosh; Maya Gupta; Lily Kerketta; Manisha Madkaikar; Suchitra Swaminathan; Baburao Vundinti
FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India.
Annals of hematology 2012;91(11):1703-12.
2012: B Kulkarni; Kanjaksha Ghosh; S Kanakia; S Shetty
Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.
Annals of hematology 2012;91(10):1667-8.
2012: Vandana D Pradhan; A Rajadhyaksha; P Surve; S Dighe; G Mahant; M Patwardhan; Kanjaksha Ghosh
Anti-C1q antibodies and their association with complement components in Indian systemic lupus erythematosus patients.
Indian journal of nephrology 2012;22(5):353-7.
2012: P Pinto; Kanjaksha Ghosh; Shrimati Shetty
Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients.
Haemophilia : the official journal of the World Federation of Hemophilia 2012;18(5):794-7.
2012: Navin Pai; Kanjaksha Ghosh; Shrimati Shetty
Hereditary protein C deficiency in Indian patients with venous thrombosis.
Annals of hematology 2012;91(9):1471-6.
2012: Selma D'Silva; Kanjaksha Ghosh; Roshan B Colah; Malay B Mukherjee
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2012;25(9):1833-4.
2012: Prashant Warang; Kanjaksha Ghosh; Prabhakar Kedar; Roshan B Colah
Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
International journal of hematology 2012;96(2):263-7.
2012: Khushnooma Italia; Anita H Nadkarni; Pratibha Sawant; Reema R Surve; Mahrukh R Wadia; Kanjaksha Ghosh; Roshan B Colah
Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population.
European journal of haematology 2012;89(2):160-4.
2012: A C Gorakshkar; Kanjaksha Ghosh
Subclinical iron deficiency is a silent epidemic amongst voluntary blood donors.
Transfusion medicine (Oxford, England) 2012;22(4):300-1.
2012: Kanjaksha Ghosh; Shrimati Shetty
Bone health in persons with haemophilia: a review.
European journal of haematology 2012;89(2):95-102.
2012: Kanjaksha Ghosh; Shrimati Shetty
Malignancies in persons with haemophilia: 25-year data from India.
The National medical journal of India 2012;25(4):251-2.
2012: Khushnooma Italia; Anita Nadkarni; Pratibha Sawant; Jayesh Sheth; Kanjaksha Ghosh; Roshan Colah
Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at risk.
Prenatal diagnosis 2012;32(7):703-7.
2012: Dipti S Upadhye; Kanjaksha Ghosh; Dipty Jain; Anita H Nadkarni; Sona B Nair; Roshan B Colah
First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
Journal of clinical pathology 2012;65(7):654-9.
2012: Navin Pai; Kanjaksha Ghosh; Shrimati Shetty
Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2012;23(4):257-61.
2012: Vivian Lobo; Shrimati Shetty; Bipin Kulkarni; Kanjaksha Ghosh
A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
Annals of hematology 2012;91(6):917-21.
2012: P Warang; Kanjaksha Ghosh; Prabhakar Kedar; Roshan B Colah
A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA reader.
International journal of laboratory hematology 2012;34(3):232-6.
2012: Vandana D Pradhan; Prathamesh Surve; Swaptagni Das; Kanjaksha Ghosh
Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus.
Indian journal of human genetics 2012;18(2):155-60.
2012: Shantashri Vaidya; Babu Rao Vundinti; Susan Idicula-Thomas; Archana Sonawani; Kanjaksha Ghosh
Imatinib resistance due to a novel tri-nucleotide insertion in the SH2/C lobe interface of BCR/ABL kinase domain between position K357 and N358.
Leukemia research 2012;36(5):e110-2.
2012: Babu Rao Vundinti; S Korgaonkar; Kanjaksha Ghosh
De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Gene 2012;498(1):128-30.
2012: Ajit C Gorakshakar; Anita H Nadkarni; Priyanka Sathe; Roshan Colah; Kanjaksha Ghosh
Hemoglobin Showa-Yakushiji: a common β thalassemia mutation among the Agri community from western India.
Genetic testing and molecular biomarkers 2012;16(4):302-5.
2012: Nikesh Kawankar; Lily Kerketta; S Korgaonkar; Manisha Madkaikar; Kanjaksha Ghosh; Farah Jijina; Babu Rao Vundinti
DNA copy number changes and immunophenotype pattern in karyotypically normal acute myeloid leukemia patients from an Indian population.
Genetic testing and molecular biomarkers 2012;16(4):265-70.
2012: P Kanani; S M Kapali; B S Poudyal; Shrimati Shetty; Kanjaksha Ghosh
Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population.
Haemophilia : the official journal of the World Federation of Hemophilia 2012;18(2):e44-5.
2012: Kanjaksha Ghosh; Kinjalka Ghosh; Shrimati Shetty
Hemostasis research in India: past, present, and future.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2012;18(2):128-33.
2012: Preethi S Nair; S Shetty; Kanjaksha Ghosh
A homozygous female hemophilia A.
Indian journal of human genetics 2012;18(1):134-6.
2012: Edna D'Souza; Kanjaksha Ghosh; Anita H Nadkarni; Sona Nair; Roshan B Colah
SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India.
Indian journal of human genetics 2012;18(1):87-90.
2012: Malay B Mukherjee; Kanjaksha Ghosh
Explaining anthropometric variations in sickle cell disease requires a multidimensional approach.
Indian journal of human genetics 2012;18(1):1-2.
2012: Dipty L Jain; Anita H Nadkarni; Vijaya Sarathi; Dipty Upadhye; Kanjaksha Ghosh; Rohini Gulhane; Roshan B Colah
Newborn screening shows a high incidence of sickle cell anemia in Central India.
Hemoglobin 2012;36(4):316-22.
2012: Khushnooma Y Italia; Anita H Nadkarni; Pratibha M Sawant; Kanjaksha Ghosh; Roshan B Colah
Is the poly A (T>C) mutation a causative factor for misdiagnosis in second trimester prenatal diagnosis of β-thalassemia by fetal blood analysis on high performance liquid chromatography?
Hemoglobin 2012;36(2):114-23.
2011: Shantashri Vaidya; Kanjaksha Ghosh; Babu Rao Vundinti
Recent developments in drug resistance mechanism in chronic myeloid leukemia: a review.
European journal of haematology 2011;87(5):381-93.
2011: Kanjaksha Ghosh; K Ghosh; J R Chowdhury
Tuberculosis and female reproductive health.
Journal of postgraduate medicine 2011;57(4):307-13.
2011: Babu Rao Vundinti; Kanjaksha Ghosh
Incidence of down syndrome: Hypotheses and reality.
Indian journal of human genetics 2011;17(3):117-9.
2011: Shankarkumar Umapathy; J P Devaraj; Kanjaksha Ghosh; D Khuperkar; R Mitra; Aruna Pawar; U Khopkar
Hla-a and hla-B alleles associated in psoriasis patients from mumbai, Western India.
Indian journal of dermatology 2011;56(5):497-500.
2011: S Shanbhag; Shrimati Shetty; Kanjaksha Ghosh
Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia : the official journal of the World Federation of Hemophilia 2011;17(5):e843-5.
2011: Vandana D Pradhan; Anita Nadkarni; Manisha Patwardhan; Kanjaksha Ghosh
Fc γ R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients.
The Indian journal of medical research 2011;134():181-5.
2011: Shrimati Shetty; Priyanka Kasatkar; Kanjaksha Ghosh
Pathophysiology of acquired von Willebrand disease: a concise review.
European journal of haematology 2011;87(2):99-106.
2011: Nikesh Kawankar; Kanjaksha Ghosh; Farah Jijina; Babu Rao Vundinti
Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.
Cancer epidemiology 2011;35(4):e1-5.
2011: Kanjaksha Ghosh; Shrimati Shetty
Epidemiology, diagnosis, and management of von Willebrand disease in India.
Seminars in thrombosis and hemostasis 2011;37(5):595-601.
2011: Babu Rao Vundinti; Lily Kerketta; S Korgaonkar; Kanjaksha Ghosh
A rare case of B-cell chronic lymphocytic leukemia with t(2;14)(p13;q32), +X, +11, +12, +13,+der(1p) karyotype.
Indian journal of cancer 2011;48(3):387-8.
2011: Manisha Madkaikar; Snehal Mhatre; Maya Gupta; Kanjaksha Ghosh
Advances in autoimmune lymphoproliferative syndromes.
European journal of haematology 2011;87(1):1-9.
2011: Atanu Basu; Divija Deshpande; Shobha Gangodkar; Ketaki Ganti; Preksha Jain; Payel Sarkar; Shrimati Shetty; Kanjaksha Ghosh
Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein.
FEMS immunology and medical microbiology 2011;62(2):140-7.
2011: S Shanbhag; Shrimati Shetty; B Kulkarni; Kanjaksha Ghosh
An improved, semi quantitative clot based assay for factor XIII.
Haemophilia : the official journal of the World Federation of Hemophilia 2011;17(4):718-20.
2011: Kanjaksha Ghosh
Haematology research in India: past, present and future.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2011;27(2):55-64.
2011: Aruna Shankarkumar; Umapathy Shankarkumar; Kanjaksha Ghosh
CCR5 chemokine receptor polymorphism in patients with HIV-1 from Western India.
Journal of acquired immune deficiency syndromes (1999) 2011;57(2):e21.
2011: Shrimati Shetty; Kanjaksha Ghosh
Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review.
Thrombosis research 2011;127(6):505-12.
2011: Shantashri Vaidya; Kanjaksha Ghosh; Manisha Madkaikar; Babu Rao Vundinti
Deletion of ABL/BCR on der(9) associated with severe basophilia.
Indian journal of human genetics 2011;17(2):100-3.
2011: Babu Rao Vundinti; Kanjaksha Ghosh
Chromosomal aberrations in hematological malignancies: A guide to the identification of novel oncogenes.
Indian journal of human genetics 2011;17(2):43-4.
2011: Prashant Warang; Maya Gupta; Prabhakar Kedar; Kanjaksha Ghosh; Roshan Colah
Flow cytometric osmotic fragility--an effective screening approach for red cell membranopathies.
Cytometry. Part B, Clinical cytometry 2011;80(3):186-90.
2011: Kanjaksha Ghosh; Shrimati Shetty
Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands?
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011;22(3):241-2.
2011: Selma D'Silva; Vikrant Borse; Roshan B Colah; Kanjaksha Ghosh; Malay B Mukherjee
Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adults.
Genetic testing and molecular biomarkers 2011;15(4):215-8.
2011: Shrimati Shetty; Manali Bhave; Kanjaksha Ghosh
Acquired hemophilia a: diagnosis, aetiology, clinical spectrum and treatment options.
Autoimmunity reviews 2011;10(6):311-6.
2011: Prabhakar S Kedar; Prashant Warang; Kanjaksha Ghosh; Roshan B Colah
Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations.
American journal of hematology 2011;86(3):327-9.
2011: Shrimati Shetty; Manali Bhave; Kanjaksha Ghosh
Challenges of multiple mutations in individual patients with haemophilia.
European journal of haematology 2011;86(3):185-90.
2011: Manisha Rajan Madkaikar; Anthony Marinaki; Prashant Utage; Lynette Fairbanks; Kanjaksha Ghosh; Shilpa Kulkarni; Mukesh Desai
Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.
BMJ case reports 2011;2011():.
2011: Kanjaksha Ghosh; Ajit C Gorakshakar
Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?
Indian journal of human genetics 2011;17(1):1-2.
2011: S Korgaonkar; Kanjaksha Ghosh; Babu Rao Vundinti
A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotype.
Journal of human reproductive sciences 2011;4(1):53-5.
2011: Shankarkumar Umapathy; Vanita Ramrakhiyani; Aruna Shankarkumar; Kanjaksha Ghosh
Role of anti-human lymphocyte culture cytotoxic antibodies in recurrent spontaneous pregnancy loss women.
Journal of human reproductive sciences 2011;4(1):17-9.
2011: Rati Chalvam; Roshan B Colah; Dipika Mohanty; Kanjaksha Ghosh; Malay B Mukherjee
Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in India.
Annals of human biology 2011;38(1):106-9.
2010: Preethi Satish Nair; Shrimati Shetty; Bipin Kulkarni; Kanjaksha Ghosh
Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.
Clinica chimica acta; international journal of clinical chemistry 2010;411(23-24):2004-8.
2010: Navin Pai; Shrimati Shetty; Bipin Kulkarni; Kanjaksha Ghosh
Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from India.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2010;16(6):698-700.
2010: Vandana D Pradhan; Prathamesh Surve; Kanjaksha Ghosh
Mannose binding lectin (MBL) in autoimmunity and its role in systemic lupus erythematosus (SLE).
The Journal of the Association of Physicians of India 2010;58():688-90.
2010: S Korgaonkar; Kanjaksha Ghosh; Farah Jijina; Babu Rao Vundinti
Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population.
Journal of pediatric hematology/oncology 2010;32(8):606-10.
2010: Khushnooma Y Italia; Farah F Jijina; Dipty Jain; RH Merchant; Anita H Nadkarni; Malay Mukherjee; Kanjaksha Ghosh; Roshan B Colah
The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.
Clinical biochemistry 2010;43(16-17):1329-32.
2010: S Chandrakala; Farah Jijina; Kanjaksha Ghosh
Diffuse alveolar haemorrhage with severe haemophilia.
Haemophilia : the official journal of the World Federation of Hemophilia 2010;16(6):962-4.
2010: Babu Rao Vundinti; S Korgaonkar; Kanjaksha Ghosh
Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.
Indian journal of cancer 2010;47(4):397-9.
2010: Boris E Shmukler; Prabhakar S Kedar; Prashant Warang; Mukesh Desai; Manisha Madkaikar; Kanjaksha Ghosh; Roshan B Colah; Seth L Alper
Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
American journal of hematology 2010;85(10):824-8.
2010: Malay B Mukherjee; Anita H Nadkarni; Ajit C Gorakshakar; Kanjaksha Ghosh; Dipika Mohanty; Roshan B Colah
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India.
Indian journal of human genetics 2010;16(3):154-8.
2010: Priyanka Kasatkar; Shrimati Shetty; Kanjaksha Ghosh
Delayed vitamin K deficiency as a cause of bleeding: still a concern in the 21st century!
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2010;21(6):608-10.
2010: Kinjalka Ghosh; Kanjaksha Ghosh
Sequential serologic testing for common viral markers in blood units in India is probably not cost-effective.
Transfusion 2010;50(8):1854-5.
2010: Navin Pai; Shrimati Shetty; Kanjaksha Ghosh
Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
Annals of hematology 2010;89(8):835-6.
2010: Vandana D Pradhan; V Borse; Kanjaksha Ghosh
PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.
Journal of postgraduate medicine 2010;56(3):239-42.
2010: Shrimati Shetty; Bipin Kulkarni; Navin Pai; Preeti Mukundan; Priyanka Kasatkar; Kanjaksha Ghosh
JAK2 mutations across a spectrum of venous thrombosis cases.
American journal of clinical pathology 2010;134(1):82-5.
2010: L Mota; Shrimati Shetty; S Idicula-Thomas; Kanjaksha Ghosh
Molecular basis of factor X deficiency cases from India.
Haemophilia : the official journal of the World Federation of Hemophilia 2010;16(4):693-7.
2010: Kanjaksha Ghosh; Kinjalka Ghosh
Advances in haematological pharmacotherapy in 21st century.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2010;26(2):30-40.
2010: Roshan B Colah; Ajit C Gorakshakar; Dr. Supriya Phanasgaonkar; Edna D'Souza; Anita Nadkarni; Reema Surve; Pratibha Sawant; Dilip Master; Ramesh Patel; Kanjaksha Ghosh; Dipika Mohanty
Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat.
British journal of haematology 2010;149(5):739-47.
2010: Kanjaksha Ghosh; Ajit Gorakshakar
Integration of modern genetic knowledge and technology into public health in India.
Indian journal of human genetics 2010;16(2):45-6.
2010: Vandana D Pradhan; Neha Deshpande; Anita Nadkarni; Manisha Patwardhan; Prathamesh Surve; Kanjaksha Ghosh
Fc gamma R IIIB polymorphisms: their association with clinical manifestations and autoantibodies in SLE patients from western India.
International journal of rheumatic diseases 2010;13(2):138-43.
2010: Rajwanti K Vaswani; Praveen G Dharaskar; Swati Kulkarni; Kanjaksha Ghosh
Iron deficiency as a risk factor for first febrile seizure.
Indian pediatrics 2010;47(5):437-9.
2010: Priyanka Kasatkar; Shrimati Shetty; Kanjaksha Ghosh
VWF pseudogene: Mimics, masks and spoils.
Clinica chimica acta; international journal of clinical chemistry 2010;411(7-8):607-9.
2010: Akriti Jain; Shrimati Shetty; Bipin Kulkarni; Kanjaksha Ghosh
Association of factor VII gene polymorphisms with Budd Chiari syndrome.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2010;21(3):296-7.
2010: V Meera; Farah Jijina; Kanjaksha Ghosh
Pulmonary hypertension in patients with hematological disorders following splenectomy.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2010;26(1):2-5.
2010: Vandana D Pradhan; Manisha M Patwardhan; Kanjaksha Ghosh
Anti-nucleosome antibodies as a disease marker in systemic lupus erythematosus and its correlation with disease activity and other autoantibodies.
Indian journal of dermatology, venereology and leprology 2010;76(2):145-9.
2010: Anita H Nadkarni; Sona B Nair; Khushnooma Y Italia; Prashant Warang; Madhura Dalvi; Kanjaksha Ghosh; Roshan B Colah
Molecular diversity of hemoglobin H disease in India.
American journal of clinical pathology 2010;133(3):491-4.
2010: S Nair; Anita H Nadkarni; P Warang; A Bhave; Kanjaksha Ghosh; Roshan B Colah
Five alpha globin chain variants identified during screening for haemoglobinopathies.
European journal of clinical investigation 2010;40(3):226-32.
2010: Khushnooma Y Italia; Farah F Jijina; Rashid Merchant; Sangeeta Panjwani; Anita H Nadkarni; Pratibha M Sawant; Sona B Nair; Kanjaksha Ghosh; Roshan B Colah
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study.
Journal of clinical pathology 2010;63(2):147-50.
2010: S Korgaonkar; Kanjaksha Ghosh; Babu Rao Vundinti
Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population.
Hematology (Amsterdam, Netherlands) 2010;15(1):58-62.
2010: Shrimati Shetty; Leenam Mota; Kanjaksha Ghosh
Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency.
Clinica chimica acta; international journal of clinical chemistry 2010;411(3-4):291.
2010: Suchitra Swaminathan; Manisha Madkaikar; Kanjaksha Ghosh; Babu Rao Vundinti; Lily Kerketta; Maya Gupta
Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation.
European journal of haematology 2010;84(2):180-2.
2010: Khushnooma Y Italia; Farah F Jijina; S Chandrakala; Anita H Nadkarni; Pratibha Sawant; Kanjaksha Ghosh; Roshan B Colah
Exposure to hydroxyurea during pregnancy in sickle-beta thalassemia: a report of 2 cases.
Journal of clinical pharmacology 2010;50(2):231-4.
2010: Vandana Pradhan; Manisha Patwardhan; Anita Nadkarni; Kanjaksha Ghosh
Fc γ RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India.
Autoimmune diseases 2010;2010():470695.
2010: Kanjaksha Ghosh
Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
Indian journal of human genetics 2010;16(1):6-7.
2010: Shobha Gangodkar; Preksha Jain; Nishikant Dixit; Kanjaksha Ghosh; Atanu Basu
Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure imaged by electron tomography and whole-mount grid-cell culture techniques.
Journal of electron microscopy 2010;59(6):503-11.
2010: Prashant Warang; Sona Nair; Anita Nadkarni; Kanjaksha Ghosh; Roshan B Colah
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches.
Hemoglobin 2010;34(1):45-8.
2010: Kanjaksha Ghosh; Shrimati Shetty; D Sahu
Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI).
Haemophilia : the official journal of the World Federation of Hemophilia 2010;16(1):61-5.
2009: Babu Rao Vundinti; Seema Korgaonkar; Kanjaksha Ghosh
Familial small supernumerary marker chromosome (sSMC) (14)(:p11-q11:) [corrected] in a child with translocation Down syndrome.
Indian journal of pediatrics 2009;76(12):1265-7.
2009: Manisha Madkaikar; Maya Gupta; Farah Jijina; Kanjaksha Ghosh
Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations.
European journal of haematology 2009;83(6):503-11.
2009: Rachita Misri; Uday Khopkar; Shankarkumar Umapathy; Kanjaksha Ghosh
Comparative case control study of clinical features and human leukocyte antigen susceptibility between familial and nonfamilial vitiligo.
Indian journal of dermatology, venereology and leprology 2009;75(6):583-7.
2009: Leenam Mota; Shrimati Shetty; Susan Idicula-Thomas; Kanjaksha Ghosh
Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
Clinica chimica acta; international journal of clinical chemistry 2009;409(1-2):106-11.
2009: Kanjaksha Ghosh; Shrimati Shetty; Sonal Vora
Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2009;107(2):159-60.
2009: Kanjaksha Ghosh; Shrimati Shetty
Immune response to FVIII in hemophilia A: an overview of risk factors.
Clinical reviews in allergy & immunology 2009;37(2):58-66.
2009: Kanjaksha Ghosh; Ajit C Gorakshakar
Genetics of autism and mental retardation: A spoonful from the sea!
Indian journal of human genetics 2009;15(3):85-7.
2009: Rati Chalvam; Roshan B Colah; Dipika Mohanty; Kanjaksha Ghosh; Malay B Mukherjee
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Blood cells, molecules & diseases 2009;43(2):156-7.
2009: Shrimati Shetty; S Vora; B Kulkarni; L Mota; Kanjaksha Ghosh
Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency: cause, consequence or a consequential cause?
Haemophilia : the official journal of the World Federation of Hemophilia 2009;15(5):1104-8.
2009: Khushnooma Y Italia; Farah J Jijina; Rashid Merchant; Sangeeta Panjwani; Anita H Nadkarni; Pratibha M Sawant; Sona B Nair; Kanjaksha Ghosh; Roshan B Colah
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.
Clinica chimica acta; international journal of clinical chemistry 2009;407(1-2):10-5.
2009: Babu Rao Vundinti; Lily Kerketta; Farah Jijina; Kanjaksha Ghosh
Cytogenetic study of myelodysplastic syndrome from India.
The Indian journal of medical research 2009;130(2):155-9.
2009: Gnanasekaran Prabu; Yagneshwar S Iyer; Umapathy Shankarkumar; Kanjaksha Ghosh; Vasanthi Nachiappan
Monoclonal antibody produced against calf thymus histone.
Hybridoma (2005) 2009;28(4):277-80.
2009: Umapathy Shankarkumar; Krishnakumar N Shah; Kanjaksha Ghosh
Letter: HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India.
Epilepsia 2009;50(7):1837-8.
2009: Vandana D Pradhan; Kanjaksha Ghosh
Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
Indian journal of dermatology 2009;54(3):258-62.
2009: Shrimati Shetty; Kanjaksha Ghosh
Anti-phospholipid antibodies and other immunological causes of recurrent foetal loss--a review of literature of various therapeutic protocols.
American journal of reproductive immunology (New York, N.Y. : 1989) 2009;62(1):9-24.
2009: Kanjaksha Ghosh; Manisha Patwardhan; Vandana Pradhan
Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas.
Rheumatology international 2009;29(9):1047-50.
2009: Kanjaksha Ghosh; Leera Quadros; Shrimati Shetty
Spectrum of factor IX gene mutations causing haemophilia B from India.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009;20(5):333-6.
2009: Kanjaksha Ghosh; V Meera; Farah Jijina
Pulmonary hypertension in patients with hematological disorders following splenectomy.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2009;25(2):45-8.
2009: Kanjaksha Ghosh; Cecil Ross
The teacher and the taught: medical education in India at the crossroads.
The National medical journal of India 2009;22(3):147-9.
2009: Kanjaksha Ghosh; Shrimati Shetty; Mukesh Tulsiani
Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009;15(3):277-82.
2009: Roshan B Colah; Ajit Gorakshakar; Anita Nadkarni; Dr. Supriya Phanasgaonkar; Reema Surve; Pratibha Sawant; Dipika Mohanty; Kanjaksha Ghosh
Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
Blood cells, molecules & diseases 2009;42(3):241-6.
2009: Kanjaksha Ghosh; Shrimati Shetty; Leera Quadros; Bipin Kulkarni
Double mutations causing haemophilia B: a double whammy!
British journal of haematology 2009;145(3):433-5.
2009: Edna D'Souza; Kanjaksha Ghosh; Roshan Colah
A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies.
Cytometry. Part B, Clinical cytometry 2009;76(3):175-80.
2009: Navin Pai; Shrimati Shetty; Susan Idicula-Thomas; Bipin Kulkarni; Kanjaksha Ghosh
Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.
Thrombosis and haemostasis 2009;101(4):785-7.
2009: Leera Quadros; Kanjaksha Ghosh; Shrimati Shetty
Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes.
Journal of pediatric hematology/oncology 2009;31(3):157-60.
2009: S Vora; Shrimati Shetty; M Khare; Kanjaksha Ghosh
Placental histomorphology in unexplained foetal loss with thrombophilia.
The Indian journal of medical research 2009;129(2):144-9.
2009: Manasi Vijapurkar; Kanjaksha Ghosh; Shrimati Shetty
Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India.
Platelets 2009;20(1):35-40.
2009: Kanjaksha Ghosh; B Kulkarni; Shrimati Shetty; S Nair
Antiplatelet antibodies in cases of Glanzmann's thrombasthenia with and without a history of multiple platelet transfusion.
Indian journal of human genetics 2009;15(1):23-7.
2009: Babu Rao Vundinti; Kanjaksha Ghosh
Chromosomal instability and cancer: An insight into the rhythm of life.
Indian journal of human genetics 2009;15(1):1-2.
2009: Anita Nadkarni; Ajit Gorakshakar; Reema Surve; Pratibha Sawant; Dr. Supriya Phanasgaonkar; Sona Nair; Kanjaksha Ghosh; Roshan B Colah
Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009;33(1):59-65.
2009: Khushnooma Italia; Dipty Jain; Sushma Gattani; Farah Jijina; Anita Nadkarni; Pratibha Sawant; Sona Nair; Dipika Mohanty; Kanjaksha Ghosh; Roshan B Colah
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
Blood cells, molecules & diseases 2009;42(1):25-31.
2009: M Vijapurkar; L Mota; Shrimati Shetty; Kanjaksha Ghosh
Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent.
Haemophilia : the official journal of the World Federation of Hemophilia 2009;15(1):199-202.
2008: Kanjaksha Ghosh; Kinjalka Ghosh
Management of chronic synovitis in patients with hemophilia: with special reference to developing countries.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2008;24(4):151-4.
2008: Kanjaksha Ghosh
Evolution and selection of human leukocyte antigen alleles by Plasmodium falciparum infection.
Human immunology 2008;69(12):856-60.
2008: Kinjalka Ghosh; Kanjaksha Ghosh
Private practice in India.
The National medical journal of India 2008;21(6):328-9.
2008: Preethi Mukundan; Shrimati Shetty; Bipin Kulkarni; Kanjaksha Ghosh
Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.
Prenatal diagnosis 2008;28(10):920-2.
2008: Sonal Vora; Shrimati Shetty; Kanjaksha Ghosh
Thrombophilic dimension of recurrent fetal loss in Indian patients.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(6):581-4.
2008: Kanjaksha Ghosh; Leenam Mota; Shrimati Shetty; Bipin Kulkarni
Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(6):577-80.
2008: Edna D'Souza; Pratibha M Sawant; Anita H Nadkarni; Ajit C Gorakshakar; Dipika Mohanty; Kanjaksha Ghosh; Roshan B Colah
Evaluation of the use of monoclonal antibodies and nested PCR for noninvasive prenatal diagnosis of hemoglobinopathies in India.
American journal of clinical pathology 2008;130(2):202-9.
2008: Kanjaksha Ghosh; Kinjalka Ghosh
Hereditary haemorrhagic telangiectasia (HHT): negotiating between the Scylla of bleeding and Charybdis of thrombosis.
Thrombosis and haemostasis 2008;100(1):162-4.
2008: Kanjaksha Ghosh; Shrimati Shetty
Deep venous thrombosis associated with antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(5):464-5.
2008: Shrimati Shetty; Kanjaksha Ghosh
Reduced clinical severity in a mutationally well-characterized cohort of severe hemophilia with associated thrombophilia.
American journal of clinical pathology 2008;130(1):84-7; quiz 146.
2008: Sonali Sadawaite; Sishir Seth; Farah Jijina; Chandran K Nair; Kanjaksha Ghosh
An unusual presentation of pediatric acute lymphoblastic leukemia.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2008;24(2):59-62.
2008: Kanjaksha Ghosh; Shrimati Shetty; Leenam Mota
Aspirin resistance in patients with coronary artery disease - which test to use in routine management?
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(4):324-6.
2008: Kanjaksha Ghosh; Shobha Gangodkar; Preksha Jain; Shrimati Shetty; Sandhya Ramjee; Pankaj Poddar; Atanu Basu
Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy.
Journal of electron microscopy 2008;57(3):113-8.
2008: Anita H Nadkarni; Dr. Supriya Phanasgaonkar; Roshan B Colah; Dipika Mohanty; Kanjaksha Ghosh
Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians.
Genetic testing 2008;12(2):177-80.
2008: Atanu Basu; Preksha Jain; Shobha V Gangodkar; Shrimati Shetty; Kanjaksha Ghosh
Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.
FEMS immunology and medical microbiology 2008;53(1):46-51.
2008: Kanjaksha Ghosh; Shrimati Shetty; Leenam Mota
Falciparum malaria selected while HIV-1 slaughtered.
Indian journal of human genetics 2008;14(2):70.
2008: Sonal Vora; Shrimati Shetty; Vinita Salvi; Purnima Satoskar; Kanjaksha Ghosh
Thrombophilia and unexplained pregnancy loss in Indian patients.
The National medical journal of India 2008;21(3):116-9.
2008: Vaibhav S Banait; M S Sandeep; Shrimati Shetty; Mukta R Bapat; Pravin M Rathi; Kanjaksha Ghosh; Dipika Mohanty; Philip Abraham
Hypercoagulable state in idiopathic ulcerative colitis: role of hyperhomocysteinemia and hyperfibrinogenemia.
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2008;27(3):94-8.
2008: Manasi Vijapurkar; Kanjaksha Ghosh; Shrimati Shetty; Mary Ann McLane; Ana Maria Moura da Silva; Diego Butera
A simple, novel and robust test to diagnose type I Glanzmann thrombasthenia.
Haematologica 2008;93(5):797-8.
2008: Prabhakar Kedar; Prashant Warang; Anita H Nadkarni; Roshan B Colah; Kanjaksha Ghosh
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood cells, molecules & diseases 2008;40(3):323-7.
2008: Sumeet Gujral; P G Subramanian; Nikhil Patkar; Y Badrinath; Ashok Kumar; PRASHANT TEMBHARE; Archana Vazifdar; Shenaj Khodaiji; Manisha Madkaikar; Kanjaksha Ghosh; Mamta Yargop; Amar Dasgupta
Report of proceedings of the national meeting on "Guidelines for Immunophenotyping of Hematolymphoid Neoplasms by Flow Cytometry".
Indian journal of pathology & microbiology 2008;51(2):161-6.
2008: S Kulkarni; R Colah; A Gorakshakar; S Gupte; K Vasantha; Dipika Mohanty; Kanjaksha Ghosh
Frequency of partial D in Western India.
Transfusion medicine (Oxford, England) 2008;18(2):91-6.
2008: Kanjaksha Ghosh; Vandana D Pradhan; Kinjalka Ghosh
Background noise of infection for using ANCA as a diagnostic tool for vasculitis in tropical and developing countries.
Parasitology research 2008;102(5):1093-5.
2008: Kanjaksha Ghosh; Shrimati Shetty; Sonal Vora; Vinita Salvi
Successful pregnancy outcome in women with bad obstetric history and recurrent fetal loss due to thrombophilia: effect of unfractionated heparin and low-molecular weight heparin.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008;14(2):174-9.
2008: Sonal Vora; Shrimati Shetty; Vinita Salvi; Purnima Satoskar; Kanjaksha Ghosh
A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss.
European journal of obstetrics, gynecology, and reproductive biology 2008;137(2):136-40.
2008: Kanjaksha Ghosh; Shrimati Shetty
Blood coagulation in falciparum malaria--a review.
Parasitology research 2008;102(4):571-6.
2008: Babu Rao Vundinti; L Kerketta; M Madkaikar; F Jijina; Kanjaksha Ghosh
Three way translocation in a new variant of t(8;21) acute myeloid leukemia involving Xp22.
Indian journal of cancer 2008;45(1):30-2.
2008: Seema Korgaonkar; Babu Rao Vundinti; Lily Kerketta; Kanjaksha Ghosh
Chromosomal breakage in myelodysplatic syndrome.
Asian Pacific journal of cancer prevention : APJCP 2008;9(1):151-4.
2008: Shankarkumar Umapathy; A Pawar; Kanjaksha Ghosh
Implications of HLA sequence-based typing in transplantation.
Journal of postgraduate medicine 2008;54(1):41-4.
2008: Kanjaksha Ghosh; Manisha Madkaikar; Farah Jijina
Spontaneous resolution of severe aplastic anemia following thymic hemorrhage.
Acta haematologica 2008;119(2):69-72.
2008: R Chalvam; Prabhakar Kedar; Roshan B Colah; Kanjaksha Ghosh; M B Mukherjee
A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
Journal of human genetics 2008;53(2):181-4.
2008: Shrimati Shetty; Kanjaksha Ghosh; Leera Quadros
Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
European journal of haematology 2008;80(1):87-9.
2007: Kanjaksha Ghosh; Shrimati Shetty; B Kulkarni
Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients.
Haemophilia : the official journal of the World Federation of Hemophilia 2007;13(6):734-9.
2007: Kanjaksha Ghosh; Kinjalka Ghosh
Pathogenesis of anemia in malaria: a concise review.
Parasitology research 2007;101(6):1463-9.
2007: Kinjalka Ghosh; Kanjaksha Ghosh
Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases.
Transactions of the Royal Society of Tropical Medicine and Hygiene 2007;101(11):1163-5.
2007: Shankarkumar Umapathy; Kanjaksha Ghosh
MHC non -HLA gene polymorphisms in transplantation.
Indian journal of pathology & microbiology 2007;50(4):881-5.
2007: Anita H Nadkarni; Reema R Surve; Roshan B Colah; Kanjaksha Ghosh; M Holay; A Dani; A Shrikhande; Vivek Bharti; S Suryawanshi
Thalassemia intermedia due to homozygosity for an Asian Indian (Agammadeltabeta) degrees deletional inversion.
Clinica chimica acta; international journal of clinical chemistry 2007;385(1-2):81-3.
2007: Lily Kerketta; Babu Rao Vundinti; Kanjaksha Ghosh
Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia.
Indian journal of human genetics 2007;13(3):125-6.
2007: Kanjaksha Ghosh
Coagulation disorders seen through the window of molecular biology.
Indian journal of human genetics 2007;13(3):81-7.
2007: Kanjaksha Ghosh; K Vasantha
Bombay phenotype in Orissa: What could we make out of it?
Indian journal of human genetics 2007;13(3):79-80.
2007: Sonal Vora; Shrimati Shetty; Kanjaksha Ghosh
Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2007;18(6):571-4.
2007: Shrimati Shetty; Sonal Vora; Bipin Kulkarni; Leenam Mota; Manasi Vijapurkar; Leera Quadros; Kanjaksha Ghosh
Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.
British journal of haematology 2007;138(4):541-4.
2007: Kanjaksha Ghosh; S Vora; S Shetty
Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis.
British journal of haematology 2007;138(4):557.
2007: S S Kulkarni; S C Gupte; K Vasantha; Dipika Mohanty; Kanjaksha Ghosh
Varied distribution of RhD epitopes in the Indian population.
The National medical journal of India 2007;20(4):169-71.
2007: Anish P Nair; Farah Jijina; Kanjaksha Ghosh; Manisha Madkaikar; Mitu Shrikhande; Manish Nema
Osteoporosis in young haemophiliacs from western India.
American journal of hematology 2007;82(6):453-7.
2007: Kanjaksha Ghosh; Amit Khare; Shrimati Shetty
Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India.
Indian heart journal 2007;59(3):242-5.
2007: Swati S Kulkarni; K Vasantha; Snehalata C Gupte; Dipika Mohanty; Kanjaksha Ghosh
Potential of commercial anti-D reagents in the identification of partial D variants in Indian population.
The Indian journal of medical research 2007;125(5):641-4.
2007: Kanjaksha Ghosh; Manisha Madkaikar; Farah Jijina; Shrimati Shetty
Fractures of long bones in severe haemophilia.
Haemophilia : the official journal of the World Federation of Hemophilia 2007;13(3):337-9.
2007: Leera Quadros; Kanjaksha Ghosh; Shrimati Shetty
A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population.
Annals of hematology 2007;86(5):377-9.
2007: Shankarkumar Umapathy; Shankarkumar Umapathy; Kanjaksha Ghosh
Specific human leukocyte antigen alleles associated with HIV-1 infection in an Indian population.
Journal of acquired immune deficiency syndromes (1999) 2007;44(4):489-90.
2007: Kanjaksha Ghosh; Kinjalka Ghosh
Microarray genetic screening: the other side of the coin.
Lancet 2007;369(9566):992.
2007: Leenam Mota; Kanjaksha Ghosh; Shrimati Shetty
Second trimester antenatal diagnosis in rare coagulation factor deficiencies.
Journal of pediatric hematology/oncology 2007;29(3):137-9.
2007: Shrimati Shetty; Kanjaksha Ghosh
Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders.
Haemophilia : the official journal of the World Federation of Hemophilia 2007;13(2):172-7.
2007: R Chalvam; M B Mukherjee; Roshan B Colah; D Mohanty; Kanjaksha Ghosh
G6PD Namoru (208 T--> C) is the major polymorphic variant in the tribal populations in southern India.
British journal of haematology 2007;136(3):512-3.
2007: Kanjaksha Ghosh; Amit Khare; Shrimati Shetty; Bipin Kulkarni
Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern of response to oral folic acid, vitamin B12, B6 therapy.
Clinica chimica acta; international journal of clinical chemistry 2007;377(1-2):281-2.
2007: Babu Rao Vundinti; Lily Kerketta; S Korgaonkar; Kanjaksha Ghosh
Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3).
Indian journal of human genetics 2007;13(1):33-5.
2007: Dr. Supriya Phanasgaonkar; Roshan B Colah; Kanjaksha Ghosh; Dipika Mohanty; S Gupte
Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India.
British journal of biomedical science 2007;64(4):160-3.
2007: M Madkaikar; M Gupta; Kanjaksha Ghosh; S Swaminathan; L Sonawane; Dipika Mohanty
Optimising methods of red cell sedimentation from cord blood to maximise nucleated cell recovery prior to cryopreservation.
British journal of biomedical science 2007;64(4):157-9.
2007: Babu Rao Vundinti; Lily Kerketta; S Korgaonkar; Kanjaksha Ghosh
Differentiation of Nijmegen breakage syndrome from Fanconi anemia.
Genetics and molecular research : GMR 2007;6(3):622-6.
2007: Prabhakar Kedar; S Nampoothiri; S Sreedhar; Kanjaksha Ghosh; K Shimizu; H Kanno; Roshan B Colah
First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.
Genetics and molecular research : GMR 2007;6(2):470-5.
2007: Manisha Madkaikar; Kanjaksha Ghosh; Maya Gupta; Suchitra Swaminathan; Dipika Mohanty
Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells.
Acta haematologica 2007;118(3):153-9.
2007: Sonal Vora; Kanjaksha Ghosh; Shrimati Shetty; Vinita Salvi; Purnima Satoskar
Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
Thrombosis journal 2007;5():9.
2006: Kanjaksha Ghosh
Iron deficiency in healthy blood donors exposes vulnerability of the nation to iron deficiency.
The Indian journal of medical research 2006;124(6):611-2.
2006: Shrimati Shetty; Kanjaksha Ghosh; Farah Jijina
First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India.
Prenatal diagnosis 2006;26(11):1015-7.
2006: Kanjaksha Ghosh
Plasma homocysteine level and myocardial infarction: how high is high enough to need intervention?
Southern medical journal 2006;99(8):796-7.
2006: Luca Monaldini; Rosanna Asselta; Stefano Duga; Flora Peyvandi; Kanjaksha Ghosh; Massimo Malcovati; Maria Luisa Tenchini
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.
Haematologica 2006;91(5):628-33.
2006: Kanjaksha Ghosh
Algorithm for recall of HIV reactive blood donors.
Journal of postgraduate medicine 2006;52(2):91.
2006: Kanjaksha Ghosh; Amit Khare; Shrimati Shetty; Sona Nair; B Kulkarni; Dipika Mohanty
Flowcytometric evidence of platelet activation in patients on aspirin following myocardial infarction.
The National medical journal of India 2006;19(2):73-4.
2006: Kanjaksha Ghosh; Sonal Vora; Shrimati Shetty
Thrombophilia and pregnancy loss--picking up a needle from the haystack!
American journal of obstetrics and gynecology 2006;194(3):900; author reply 901.
2006: Babu Rao Vundinti; Lily Kerketta; Manisha Madkaikar; J Farah; Kanjaksha Ghosh
Hybrid cytogenetics of chronic lymphocytic leukemia and follicular cell lymphoma in a case of non-Hodgkin's lymphoma.
Acta haematologica 2006;116(2):150-2.
2006: Bipin Kulkarni; Sona Nair; Shrimati Shetty; Kanjaksha Ghosh
Diagnostic pitfalls and fallacies of measuring antiplatelet antibodies.
Acta haematologica 2006;116(1):75-6.
2006: Kanjaksha Ghosh; Sucheta Trasi; Shrimati Shetty; Dipika Mohanty
Use of a new enzyme-linked immunosorbent assay for the detection of type 2N von Willebrand disease and its prevalence in an Indian population.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2006;17(1):7-11.
2006: Kanjaksha Ghosh
Non haematological effects of iron deficiency - a perspective.
Indian journal of medical sciences 2006;60(1):30-7.
2006: Sucheta Trasi; Dipika Mohanty; Anil Pathare; Shrimati Shetty; Kanjaksha Ghosh
Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection in von Willebrand disease families in the Indian population.
Acta haematologica 2006;115(1-2):64-7.
2005: Kanjaksha Ghosh; A P Nair; Farah Jijina; Manisha Madkaikar; Shrimati Shetty; Dipika Mohanty
Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country.
Haemophilia : the official journal of the World Federation of Hemophilia 2005;11(5):459-62.
2005: Dipika Mohanty; Kanjaksha Ghosh; Shrimati Shetty; Marta Spreafico; Isabella Garagiola; Flora Peyvandi
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.
American journal of hematology 2005;79(4):262-6.
2005: Shankarkumar Umapathy; Kanjaksha Ghosh; D Mohanty
Molecular diversity of HLA-Cw alleles in the Maratha community of Mumbai, Maharashtra, western India.
International journal of immunogenetics 2005;32(4):223-7.
2005: Sucheta Trasi; Dipika Mohanty; Shrimati Shetty; Kanjaksha Ghosh
Prenatal diagnosis of von Willebrand disease in a family.
The National medical journal of India 2005;18(4):187-8.
2005: Vandana D Pradhan; Suresh S Badakere; Kanjaksha Ghosh; A Almeida
ANCA: serology in Wegener's granulomatosis.
Indian journal of medical sciences 2005;59(7):292-300.
2005: Prabhakar Kedar; Anita H Nadkarni; Supriya Phanasgoankar; Manisha Madkaikar; Kanjaksha Ghosh; Ajit C Gorakshakar; Roshan B Colah; Dipika Mohanty
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.
American journal of hematology 2005;79(2):168-70.
2005: Amit Khare; Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty; S Chatterjee
Evaluation of markers of endothelial damage in cases of young myocardial infarction.
Atherosclerosis 2005;180(2):375-80.
2005: Lily Kerketta; Babu Rao Vundinti; Manisha Madkaiker; Kanjaksha Ghosh; Dipika Mohanty; Farah Jijina
Biphenotypic expression in a case of acute leukemia with pericentric inv(6)(p12q24).
Cancer genetics and cytogenetics 2005;159(2):187-9.
2005: Kanjaksha Ghosh; Amit Khare; Shrimati Shetty
Implications of human genome and modern cell biology research in management of cardiovascular diseases.
Indian heart journal 2005;57(3):270-3.
2005: Sucheta Trasi; Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Prevalence and spectrum of von Willebrand disease from western India.
The Indian journal of medical research 2005;121(5):653-8.
2005: Shankarkumar Umapathy; Kanjaksha Ghosh; Vandana D Pradhan; Suresh S Badakere; Dipika Mohanty
Immunogenetic association in patients with antineutrophil cytoplasmic antibodies (ANCA) from Mumbai, Maharashtra, India.
Journal of autoimmunity 2005;24(3):227-33.
2005: Sucheta A Trasi; Anil V Pathare; Shrimati D Shetty; Kanjaksha Ghosh; Vinita Salvi; Dipika Mohanty
The spectrum of bleeding disorders in women with menorrhagia: a report from Western India.
Annals of hematology 2005;84(5):339-42.
2005: B Kulkarni; D Mohanty; Kanjaksha Ghosh
Frequency distribution of human platelet antigens in the Indian population.
Transfusion medicine (Oxford, England) 2005;15(2):119-24.
2005: Sucheta Trasi; Kanjaksha Ghosh; Shrimati Shetty; Dipika Mohanty
von Willebrand disease: a laboratory approach.
The National medical journal of India 2005;18(2):78-84.
2005: Kanjaksha Ghosh; S Nair; S Shetty; M Rajapurkar; D Mohanty
Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: a unified pathology?
Platelets 2005;16(2):85-9.
2005: Sona Nair; Kanjaksha Ghosh; Shrimati Shetty; Dipika Mohanty
Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients.
Journal of thrombosis and haemostasis : JTH 2005;3(3):482-8.
2005: Babu Rao Vundinti; Lily Kerketta; S Korgaonkar; Kanjaksha Ghosh; Dipika Mohanty
Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
Genetic counseling (Geneva, Switzerland) 2005;16(2):139-43.
2004: Sona Nair; Kanjaksha Ghosh; Shrimati Shetty; Dipika Mohanty
A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patient.
Haematologica 2004;89(12):1529-30.
2004: Kanjaksha Ghosh; S Shetty
Anticoagulation in haemophilia patients with prosthetic valve replacement.
Haemophilia : the official journal of the World Federation of Hemophilia 2004;10(6):743.
2004: Roshan B Colah; Shrimati Shetty; Anita H Nadkarni; Kanjaksha Ghosh; Dipika Mohanty
Masking of the clinical severity of severe haemophilia A in a patient with beta-thalassemia major--its implications in prenatal diagnosis.
Prenatal diagnosis 2004;24(11):925-6.
2004: Soumen Khatua; Chandrika N Nair; Kanjaksha Ghosh
Immune-mediated thrombocytopenia following dactinomycin therapy in a child with alveolar rhabdomyosarcoma: the unresolved issues.
Journal of pediatric hematology/oncology 2004;26(11):777-9.
2004: Amit Khare; Kanjaksha Ghosh; Shrimati Shetty; Bipin Kulkarni; Dipika Mohanty
Combination of thrombophilia markers in acute myocardial infarction of the young.
Indian journal of medical sciences 2004;58(9):381-8.
2004: Roshan B Colah; Anita H Nadkarni; Ajit C Gorakshakar; Dr. Supriya Phanasgaonkar; Reema R Surve; P G Subramaniam; Nagnath Bondge; Kamala Pujari; Kanjaksha Ghosh; Dipika Mohanty
Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
Blood cells, molecules & diseases 2004;33(2):153-7.
2004: Dipika Mohanty; Bipin Kulkarni; Kanjaksha Ghosh; Sona Nair; Amit Khare
Human platelet specific antigens and their importance.
Indian pediatrics 2004;41(8):797-805.
2004: Kanjaksha Ghosh; S Shetty; D Mohanty
Inversion of intron 1 is a rare cause of severe hemophilia A in Indian population.
Journal of thrombosis and haemostasis : JTH 2004;2(8):1481-2.
2004: Kanjaksha Ghosh
Management of haemophilia and its complications in developing countries.
Clinical and laboratory haematology 2004;26(4):243-51.
2004: Dipika Mohanty; Kanjaksha Ghosh; Amit Khare; Bipin Kulkarni
Thrombophilia in coronary artery disease: a double jeopardy.
The Indian journal of medical research 2004;120(1):13-23.
2004: Vandana D Pradhan; Suresh S Badakere; Kanjaksha Ghosh; Shankarkumar Umapathy
Spectrum of anti-neutrophil cytoplasmic antibodies in patients with pulmonary tuberculosis overlaps with that of Wegener's granulomatosis.
Indian journal of medical sciences 2004;58(7):283-8.
2004: Prabhakar Kedar; Roshan B Colah; Kanjaksha Ghosh; Dipika Mohanty
Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case.
Clinica chimica acta; international journal of clinical chemistry 2004;344(1-2):221-4.
2004: Malay B Mukherjee; Reema R Surve; Raman R Gangakhedkar; Kanjaksha Ghosh; Roshan B Colah; Dipika Mohanty
Beta-globin gene cluster haplotypes linked to the betaS gene in western India.
Hemoglobin 2004;28(2):157-61.
2004: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Major disorganization of factor VIII gene as a cause of severe hemophilia A in Indian patients.
American journal of hematology 2004;76(1):96.
2004: Manisha Madkaikar; Kanjaksha Ghosh
Immunotherapy in benzene-induced aplastic anemia using a biotherapeutic approach--is it durable?
Stem cells and development 2004;13(2):161-2; author reply 162-3.
2004: Kanjaksha Ghosh; Amit Khare; Bipin Kulkarni; Shrimati Shetty; Dipika Mohanty
Geography too determines the causes of inherited thrombophilia.
Journal of thrombosis and haemostasis : JTH 2004;2(2):363-4.
2004: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Genetic disorder following assisted reproductive technology - prevent if you can, but always counsel!
British journal of haematology 2004;124(4):561.
2004: Roshan B Colah; Shrimati D Shetty; Reema R Surve; Dr. Supriya Phanasgaonkar; Anita H Nadkarni; Ajit C Gorakshakar; Kanjaksha Ghosh; Sunil J Parekh; Dipika Mohanty
Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon association.
Hemoglobin 2004;28(4):343-6.
2004: Kanjaksha Ghosh; S Shetty; F Jijina; D Mohanty
Role of epsilon amino caproic acid in the management of haemophilic patients with inhibitors.
Haemophilia : the official journal of the World Federation of Hemophilia 2004;10(1):58-62.
2003: D Mohanty; Kanjaksha Ghosh; S Shetty
Selection bias largely explains the differential distribution of factor V Leiden in different patient populations between the centers--a rebuttal.
Journal of thrombosis and haemostasis : JTH 2003;1(12):2697-8.
2003: Prabhakar Kedar; Roshan B Colah; S Kulkarni; Kanjaksha Ghosh; Dipika Mohanty
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Clinical and laboratory haematology 2003;25(6):373-6.
2003: Manisha Madkaikar; Kanjaksha Ghosh
Treating patients of myelodysplastic syndrome with antithymocytic globulin--should we be more selective?
Blood 2003;102(10):3851-2; author reply 3852.
2003: Kanjaksha Ghosh; Babu Rao Vundinti; Lily Kerketta; Manisha Madkaikar; Dipika Mohanty; Farah Jijina
Severe megakaryocytic dysplasia in a case of myelodysplasia progressing to acute megakaryocytic leukemia presenting with dic(1;16)(q21;p13.3) and t(1;22)(p13;q13).
Cancer genetics and cytogenetics 2003;146(2):176-8.
2003: F Jijina; Kanjaksha Ghosh; M Mukherjee; Dipika Mohanty
Hereditary spherocytosis in North India: need for more extensive data.
The Journal of the Association of Physicians of India 2003;51():1025; author reply 1025-6.
2003: Babu Rao Vundinti; Kerketta Lily; Korgaonkar Seema; Kanjaksha Ghosh; Mohanty Dipika
Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patient.
Annales de génétique 2003;46(4):475-8.
2003: Kanjaksha Ghosh; S Nair; B Kulkarni; S Shetty; D Mohanty
Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state.
Journal of thrombosis and haemostasis : JTH 2003;1(10):2255-6.
2003: Kanjaksha Ghosh; S Trasi; S Nair; S Shetty; D Mohanty
Prevalence of inherited bleeding disorders in cases of idiopathic menorrhagia: a case of five blind men describing an elephant.
Journal of thrombosis and haemostasis : JTH 2003;1(10):2242-3.
2003: Kanjaksha Ghosh; A Nabar; S Shetty; D Soren; D Mohanty
Is there a prethrombotic state in left atrial blood in rheumatic mitral stenosis?
American journal of hematology 2003;74(2):144.
2003: Kanjaksha Ghosh
CMV seropositivity and mycosis fungoides--the Indian perspectives.
Blood 2003;102(7):2706-7.
2003: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements.
The Journal of the Association of Physicians of India 2003;51():916-8.
2003: Kanjaksha Ghosh; Sona Nair; Bipin Kulkarni; Amit Khare; Shrimati Shetty; Dipika Mohanty
Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.
Platelets 2003;14(6):351-4.
2003: Kanjaksha Ghosh; Sona Nair; Bipin Kulkarni; Amit Khare; S Trasi; Shrimati Shetty; Dipika Mohanty
Inherited haemostatic disorders in idiopathic menorrhagia: do the special interest of a hemostatic laboratory make a difference?
Haemophilia : the official journal of the World Federation of Hemophilia 2003;9(5):660-1.
2003: S Shetty; Kanjaksha Ghosh; D Mohanty
ELISA for factor VIII antibodies: does it detect antibodies much before the conventional Bethesda assay?
Haemophilia : the official journal of the World Federation of Hemophilia 2003;9(5):654.
2003: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Direct detection of factor IX gene deletions in Indian haemophiliacs by multiplex PCR.
European journal of haematology 2003;71(3):233-4.
2003: Y S Mehta; Kanjaksha Ghosh; Suresh S Badakere; A V Pathare; Dipika Mohanty
Role of antiidiotypic antibodies on the clinical course of idiopathic thrombocytopenic purpura.
The Journal of laboratory and clinical medicine 2003;142(2):113-20.
2003: Shankarkumar Umapathy; Kanjaksha Ghosh; D Mohanty
Novel HLA B*2714 and B*2708 allele associations in seronegative spondarthritis patients and haemophilia patients with chronic synovitis in India.
Tissue antigens 2003;62(2):175-8.
2003: Babu Rao Vundinti; Manisha Madkaikar; Lily Kerketta; Farah Jijina; Kanjaksha Ghosh; Dipika Mohanty; Farah Jijina
A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome.
Cancer genetics and cytogenetics 2003;144(2):175-6.
2003: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Comparison of four commercially available activated partial thromboplastin time reagents using a semi-automated coagulometer.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003;14(5):493-7.
2003: Kanjaksha Ghosh; Farah Jijina; Dipika Mohanty
Haematuria and urolithiasis in patients with haemophilia.
European journal of haematology 2003;70(6):410-2.
2003: Shankarkumar Umapathy; Devaraj Prasanavar; Kanjaksha Ghosh; Dipika Mohanty
HLA A*02 allele frequencies and B haplotype associations in Western Indians.
Human immunology 2003;64(5):562-6.
2003: Babu Rao Vundinti; K Seema; K Lily; Kanjaksha Ghosh; Dipika Mohanty
Trisomy 22 with unusual phenotype.
Indian pediatrics 2003;40(4):371-2.
2003: Shrimati Shetty; Kanjaksha Ghosh; Shankar Anbhavne; Dipika Mohanty
Requiem to prenatal diagnosis of haemophilia A and B using coagulation activity and antigen based assays: not yet!
European journal of haematology 2003;70(4):253-4.
2003: Kanjaksha Ghosh; Manisha Madkaikar; Farah Jijina; S Gandhi; Shrimati Shetty; Dipika Mohanty
Open heart surgery with mitral valve replacement--ordeal of an undiagnosed haemophilia patient.
Clinical and laboratory haematology 2003;25(2):131-3.
2003: Kanjaksha Ghosh; Shankarkumar Umapathy; Shrimati Shetty; Dipika Mohanty
Chronic synovitis and HLA B27 in patients with severe haemophilia.
Lancet 2003;361(9361):933-4.
2003: Kanjaksha Ghosh; Yegneshwar Iyer; Atanu Basu; Manisha Madkaikar; Farah Jijina; Shankarkumar Umapathy; Dipika Mohanty
Virological, serological and haemopoietic colony studies and its correlation with the outcome of severe aplastic anemia.
The hematology journal : the official journal of the European Haematology Association / EHA 2003;4(4):292-4.
2003: Vandana D Pradhan; Suresh S Badakere; Kanjaksha Ghosh
Antihistone and other autoantibodies in beta-thalassemia major patients receiving iron chelators.
Acta haematologica 2003;109(1):35-9.
2003: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
An ELISA assay for the detection of factor VIII antibodies - comparison with the conventional Bethesda assay in a large cohort of haemophilia samples.
Acta haematologica 2003;109(1):18-22.
2003: Shankarkumar Umapathy; Kanjaksha Ghosh; Suresh S Badakere; Dipika Mohanty
HLA-DRB1*03 and DQB1*0302 associations in a subset of patients severely affected with systemic lupus erythematosus from western India.
Annals of the rheumatic diseases 2003;62(1):92-3.
2002: Sona Nair; Kanjaksha Ghosh; Bipin Kulkarni; Shrimati Shetty; Dipika Mohanty
Glanzmann's thrombasthenia: updated.
Platelets 2002;13(7):387-93.
2002: Kanjaksha Ghosh; Farah Jijina; Shrimati Shetty; Manisha Madkaikar; Dipika Mohanty
First-time development of FVIII inhibitor in haemophilia patients during the postoperative period.
Haemophilia : the official journal of the World Federation of Hemophilia 2002;8(6):776-80.
2002: Kanjaksha Ghosh; Bipin Kulkarni; Sona Nair; Shrimati Shetty; Dipika Mohanty
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease.
British journal of haematology 2002;119(2):348-53.
2002: Yasser A Wali; Zakia Al Lamki; Samir S Hussein; Hadia Bererhi; Dilip Kumar; Shah Wasifuddin; Mathew Zachariah; Kanjaksha Ghosh
Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and alpha-thalassemia trait.
Pediatric hematology and oncology 2002;19(7):491-500.
2002: Shankarkumar Umapathy; J P Devaraj; Kanjaksha Ghosh; D Karnad; K Anand; D Mohanty
HLA associations in P. falciparum malaria patients from Mumbai, western India.
Indian journal of malariology 2002;39(3-4):76-82.
2002: Vandana D Pradhan; Suresh S Badakere; Shankarkumar Umapathy; Yegneshwar Iyer; Kanjaksha Ghosh; D Karnad
Anti-neutrophil cytoplasmic antibodies (ANCA) in malaria.
Indian journal of malariology 2002;39(3-4):51-9.
2002: Shankarkumar Umapathy; Kanjaksha Ghosh; Dipika Mohanty
Defining the allelic variants of HLA A19 in the western Indian population.
Human immunology 2002;63(9):779-82.
2002: Manisha Madkaikar; Kanjaksha Ghosh; Farah Jijina; Maya Gupta; Madhvi Rajpurkar; Dipika Mohanty
Tuberculosis and immune thrombocytopenia.
Haematologica 2002;87(8):ELT38.
2002: Kanjaksha Ghosh
Thrombohaemorrhagic balance in diabetes mellitus.
Journal of the Indian Medical Association 2002;100(7):428, 430, 432-3.
2002: Shankarkumar Umapathy; Kanjaksha Ghosh; Dipika Mohanty
HLA B27 polymorphism in Western India.
Tissue antigens 2002;60(1):98-101.
2002: Shankarkumar Umapathy; Kanjaksha Ghosh; Dipika Mohanty
The human leucocyte antigen (HLA) system.
The Journal of the Association of Physicians of India 2002;50():916-26.
2002: Kanjaksha Ghosh; A K Shenoy; Zahra H Al-Mahrooqi
Bacteriological infections during the first hundred days of allogenic bone marrow transplantation--experience from Oman.
The Journal of the Association of Physicians of India 2002;50():910-2.
2002: Kanjaksha Ghosh; S Shetty; F Jijina; D Mohanty
Development of anti-VWF antibody in a patient with severe haemophilia A following the development of high-grade non-Hodgkin's lymphoma.
Clinical and laboratory haematology 2002;24(3):191-3.
2002: Kanjaksha Ghosh; S Gosavi; Anil Pathare; Manisha Madkaikar; Babu Rao Vundinti; Dipika Mohanty
Low cost autologous peripheral blood stem cell transplantation performed in a municipal hospital for a patient with plasma cell leukaemia.
Clinical and laboratory haematology 2002;24(3):187-90.
2002: Muttuswamy Sivakumaran; Kanjaksha Ghosh
Cutaneous reaction to low-molecular-weight heparin.
British journal of haematology 2002;117(2):257.
2002: Kanjaksha Ghosh; Malay B Mukherjee; U Shankar; S L Kote; SB Nagtilak; R B Kolah; Reema R Surve; AA Tamankar; S Sukumar
Clinical examination and hematological data in asymptomatic & apparently healthy school children in a boarding school in a tribal area.
Indian journal of public health 2002;46(2):61-5.
2002: Bipin Kulkarni; Dipika Mohanty; Kanjaksha Ghosh; Shankarkumar Umapathy; Amit Khare
Frequency distribution of antigens in the human platelet antigen-1 system in the western Indian population.
Transfusion 2002;42(3):317-20.
2002: Kanjaksha Ghosh; S Shetty; D Mohanty
Genomic interaction in haemophilia: uncharted territory.
Haemophilia : the official journal of the World Federation of Hemophilia 2002;8(2):157-8.
2002: U Shankar Kumar; Kanjaksha Ghosh; S S Gupte; S C Gupte; Dipika Mohanty
Role of HLA antigens in Rh (D) alloimmunized pregnant women from Mumbai, Maharashtra, India.
Journal of biosciences 2002;27(2):135-41.
2002: Kanjaksha Ghosh; Shankarkumar Umapathy; Dipika Mohanty
Common human leucocyte antigen haplotypes in Indians--its implications in finding unrelated compatible bone marrow donors.
Transfusion medicine (Oxford, England) 2002;12(1):43-8.
2002: Dipika Mohanty; Roshan B Colah; Ajit C Gorakshakar; Anita H Nadkarni; Dr. Supriya Phanasgaonkar; Shrimati Shetty; Kanjaksha Ghosh; Malay B Mukherjee
Genetic disorders in haematological practice in India.
Community genetics 2002;5(3):197-200.
2002: Prabhakar Kedar; Roshan B Colah; Kanjaksha Ghosh; Dipika Mohanty
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
Haematologia 2002;32(4):543-9.
2002: Amit Khare; Kanjaksha Ghosh; Bipin Kulkarni; Dipika Mohanty
Thrombophilia: hereditary and acquired in cardiovascular disease.
Haematologia 2002;32(4):293-311.
2002: Dipika Mohanty; Kanjaksha Ghosh; A V Pathare; D Karnad
Deferiprone (L1) as an adjuvant therapy for Plasmodium falciparum malaria.
The Indian journal of medical research 2002;115():17-21.
2002: M Manisha; Kanjaksha Ghosh; Shrimati Shetty; Sona Nair; Amit Khare; Bipin Kulkarni; Anil Pathare; S Baindur; Dipika Mohanty
Spectrum of inherited bleeding disorders from Western India.
Haematologia 2002;32(1):39-47.
2002: Prabhakar Kedar; Kanjaksha Ghosh; Roshan B Colah; Dipika Mohanty
Chronic persistent hemolysis in an infant: can we afford to forget malaria as a cause?
The hematology journal : the official journal of the European Haematology Association / EHA 2002;3(2):114-5.
2002: Shankarkumar Umapathy; J P Devraj; Kanjaksha Ghosh; D Mohanty
Seronegative spondarthritis and human leucocyte antigen association.
British journal of biomedical science 2002;59(1):38-41.
2002: Kanjaksha Ghosh; S Shetty; A Pawar; D Mohanty
Danazol therapy in factor X deficiency: more questions than answers.
Haemophilia : the official journal of the World Federation of Hemophilia 2002;8(1):61-2.
2002: Kanjaksha Ghosh; Shrimati Shetty; A Pawar; Dipika Mohanty
Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges.
Haemophilia : the official journal of the World Federation of Hemophilia 2002;8(1):51-5.
2001: A R Pawar; S Shetty; Kanjaksha Ghosh; D Mohanty
How old is factor V Leiden mutation?
Thrombosis and haemostasis 2001;86(6):1591-2.
2001: Babu Rao Vundinti; Lily Kerketta; S Korgaonkar; Kanjaksha Ghosh; Dipika Mohanty
18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype.
Annales de génétique 2001;44(4):187-90.
2001: Kanjaksha Ghosh; S Shetty; D Mohanty
Congenital deficiency of vitamin K dependent coagulation factors--its rarity and need for an international registry.
Thrombosis and haemostasis 2001;86(4):1131.
2001: D Mohanty; Shrimati Shetty; Kanjaksha Ghosh; A Pawar; P Abraham
Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India.
Hepatology (Baltimore, Md.) 2001;34(4 Pt 1):666-70.
2001: Anita H Nadkarni; Ajit C Gorakshakar; C Y Lu; Rajagopal Krishnamoorthy; Kanjaksha Ghosh; Roshan B Colah; D Mohanty
Molecular pathogenesis and clinical variability of beta-thalassemia syndromes among Indians.
American journal of hematology 2001;68(2):75-80.
2001: Kanjaksha Ghosh; Shrimati Shetty; Dipika Mohanty
Haemorrhage in upper cervical cord: an unusual manifestation in moderate haemophilia patients who ride motorbikes.
Haemophilia : the official journal of the World Federation of Hemophilia 2001;7(5):515-6.
2001: Farah Jijina; Kanjaksha Ghosh; Manisha Madkaikar; Dipika Mohanty
Ophthalmic surgery in haemophilia.
Haemophilia : the official journal of the World Federation of Hemophilia 2001;7(5):464-7.
2001: Shrimati Shetty; Kanjaksha Ghosh; S Parekh; Dipika Mohanty
Combined factor VIII and IX deficiency in a family.
Clinical and laboratory haematology 2001;23(3):201-4.
2001: Kanjaksha Ghosh; Shrimati Shetty; Bipin Kulkarni; Sona Nair; Shankarkumar Umapathy; Amit Khare; S Baindur; Dipika Mohanty
Development of inhibitors in patients with haemophilia from India.
Haemophilia : the official journal of the World Federation of Hemophilia 2001;7(3):273-8.
2001: Kanjaksha Ghosh; Shrimati Shetty; Manisha Madkaikar; Shankarkumar Umapathy; Sona Nair; Amit Khare; Anil Pathare; Farah Jijina; Dipika Mohanty
Venous thromboembolism in young patients from western India: a study.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2001;7(2):158-65.
2001: Babu Rao Vundinti; Lily Kerketta; Kanjaksha Ghosh; Dipika Mohanty
A 46, XY, dup (1) (q21q32), add(11) (q23) karyotype in a case of Fanconi anemia.
Leukemia research 2001;25(4):347-8.
2001: S Shetty; Kanjaksha Ghosh; A Bhide; D Mohanty
Carrier detection and prenatal diagnosis in families with haemophilia.
The National medical journal of India 2001;14(2):81-3.
2001: Kanjaksha Ghosh; Manisha Madkaikar; Yegneshwar Iyer; Anil Pathare; Farah Jijina; Dipika Mohanty
Systemic capillary leak syndrome preceding plasma cell leukaemia.
Acta haematologica 2001;106(3):118-21.
2001: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
Hemophilia B in a female.
Acta haematologica 2001;106(3):115-7.
2001: Roshan B Colah; Ajit C Gorakshakar; Reema R Surve; Mahrukh R Wadia; Kanjaksha Ghosh; Dipika Mohanty
Feasibility of antenatal screening of beta-thalassemia in Mumbai, India.
Acta haematologica 2001;105(4):252.
2001: Kanjaksha Ghosh; K N Javeri; Dipika Mohanty; B D Parmar; R R Surati; S H Joshi
False-positive serological tests in acute malaria.
British journal of biomedical science 2001;58(1):20-3.
2001: Kanjaksha Ghosh; Shrimati Shetty; Dipika Mohanty
Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay.
Haemophilia : the official journal of the World Federation of Hemophilia 2001;7(1):9-12.
2000: Ajit C Gorakshakar; Kanjaksha Ghosh; Roshan B Colah; D Mohanty
Beta-thalassemia gene flow from India to Mauritius.
American journal of hematology 2000;65(3):263-4.
2000: Kanjaksha Ghosh; Malay B Mukherjee; Reema R Surve; Shankarkumar Umapathy; S L Kate; SB Nagtilak; Roshan B Colah; AA Tamankar; Dipika Mohanty
Splenomegaly in school children in a remote tribal area of Dhole district, Maharashtra.
Indian journal of malariology 2000;37(3-4):68-73.
2000: Kanjaksha Ghosh; S Shetty; D Mohanty
Detection of unexpected lupus anticoagulant during preparation of normal pooled plasma (NPP) from healthy volunteers.
Thrombosis and haemostasis 2000;84(3):519-21.
2000: Shrimati Shetty; Manisha Madkaikar; Sona Nair; Shankarkumar Umapathy; S Baindur; Anil Pathare; Kanjaksha Ghosh; Dipika Mohanty
Combined factor V and VIII deficiency in Indian population.
Haemophilia : the official journal of the World Federation of Hemophilia 2000;6(5):504-7.
2000: Kanjaksha Ghosh; S H Joshi; Shrimati Shetty; Shankarkumar Umapathy; S Chipkar; V Pujari; Manisha Madkaikar; Anil Pathare; Farah Jijina; Dipika Mohanty
Transfusion transmitted diseases in haemophilics from western India.
The Indian journal of medical research 2000;112():61-4.
2000: A Pawar; Kanjaksha Ghosh; S Shetty; R Colah; D Mohanty
High frequency of factor V Leiden mutation in Parsis--a highly endogamous population in India.
Thrombosis and haemostasis 2000;83(6):965.
2000: J S Kale; Kanjaksha Ghosh; Dipika Mohanty; Anil Pathare; Farah Jijina
Use of the dual force system to correct chronic knee deformities due to severe haemophilia.
Haemophilia : the official journal of the World Federation of Hemophilia 2000;6(3):177-80.
2000: Y S Mehta; A V Pathare; Suresh S Badakere; Kanjaksha Ghosh; Dipika Mohanty
Influence of auto-antibody specificities on the clinical course in patients with chronic and acute ITP.
Platelets 2000;11(2):94-8.
2000: Reema R Surve; Malay B Mukherjee; S L Kate; SB Nagtilak; Mahrukh R Wadia; AA Tamankar; Kanjaksha Ghosh; Roshan B Colah; Dipika Mohanty
Detection of the beta s gene: an evaluation of the solubility test against automated chromatography and haemoglobin electrophoresis.
British journal of biomedical science 2000;57(4):292-4.
2000: Kanjaksha Ghosh; UD Khanduri; Devendra Hiwase; S Venugopal; David E Muirhead
Acute myelomonocytic leukaemia with pseudo-Chediak-Higashi inclusions in leukaemic blasts report of an unusual case.
Haematologia 2000;30(3):229-34.
2000: Shrimati Shetty; Kanjaksha Ghosh; Dipika Mohanty
St 14 (DX S52) VNTR polymorphism in the Indian population and its application in carrier detection and prenatal diagnosis of haemophilia A families.
Haematologia 2000;30(3):203-7.
2000: S Shetty; Kanjaksha Ghosh; A Pathare; D Mohanty
Clinically significant inhibitors in hemophilia A patients from India tend to persist.
Acta haematologica 2000;103(3):175-6.
2000: Kanjaksha Ghosh; S Daar; D Hiwase; N Nursat
Primary pseudomonas meningitis in an adult, splenectomized, multitransfused thalassaemia major patient.
Haematologia 2000;30(1):69-72.
2000: Kanjaksha Ghosh; Devendra Hiwase; David E Muirhead
Intense eosinophilia with abnormal ultrastructure as presenting manifestation of acute lymphoblastic leukemia.
Haematologia 2000;30(2):137-41.
2000: Malay B Mukherjee; Reema R Surve; Kanjaksha Ghosh; Roshan B Colah; Dipika Mohanty
Clinical diversity of sickle cell disease in western india - influence of genetic factors.
Acta haematologica 2000;103(2):122-3.
2000: Kanjaksha Ghosh; Shrimati Shetty; A Pathare; Dipika Mohanty
Epsilon-aminocaproic acid inhibits the activity of factor VIII inhibitors in patients with severe haemophilia A in vivo and in vitro.
Acta haematologica 2000;103(2):67-72.
2000: Kanjaksha Ghosh; S Mitra; Devendra Hiwase
Choroidal infiltrates simulating fundal changes of acute leukemia during hematological recovery following high-dose chemotherapy in acute myelomonocytic leukemia in remission.
American journal of hematology 2000;63(1):42-5.
1999: Kanjaksha Ghosh; Farah Jijina; Anil Pathare; Dipika Mohanty
Gas gangrene in a patient with severe haemophilia A.
Haemophilia : the official journal of the World Federation of Hemophilia 1999;5(6):450-2.
1999: Anita H Nadkarni; Kanjaksha Ghosh; Ajit C Gorakshakar; Roshan B Colah; D Mohanty
Variable clinical severity of Hb E beta-thalassemia among Indians.
The Journal of the Association of Physicians of India 1999;47(10):966-8.
1999: Kanjaksha Ghosh; S Shetty; D Mohanty
Haemophilia following successful in vitro fertilization.
Haemophilia : the official journal of the World Federation of Hemophilia 1999;5(5):364.
1999: Kanjaksha Ghosh; David E Muirhead; B Christie; Devendra Hiwase
Ultrastructural changes in peripheral blood neutrophils in a patient receiving ganciclovir for CMV pneumonitis following allogenic bone marrow transplantation.
Bone marrow transplantation 1999;24(4):429-31.
1999: K Bharucha; S Kulkarni; Sona Nair; Kanjaksha Ghosh; Dipika Mohanty; V Walvekar; V Raut
Functional and fibrinogen receptor studies in platelets in pre-eclamptic toxaemia of pregnancy.
Platelets 1999;10(4):197-202.
1999: Shrimati Shetty; Kanjaksha Ghosh; Anil Pathare; Dipika Mohanty
Carrier detection in haemophilia A families: comparison of conventional coagulation parameters with DNA polymorphism analysis - first report from India.
Haemophilia : the official journal of the World Federation of Hemophilia 1999;5(4):243-6.
1999: Kanjaksha Ghosh; B Rafique; J Tirkey; E Benjamin; S Jacob; J Goes
Successful non-invasive ventilatory support in a patient with regimen-related toxicity during allogeneic bone marrow transplantation.
Bone marrow transplantation 1999;23(8):833-4.
1999: Kanjaksha Ghosh; M Ayyalil
Engraftment of allogeneic marrow following conditioning the donor with G-CSF.
Acta haematologica 1999;102(2):110-2.
1998: Kanjaksha Ghosh; M Ayyaril; Vadakkepat Nirmala
Acute GVHD involving the gastrointestinal tract and infestation with Blastocystis hominis in a patient with chronic myeloid leukaemia following allogeneic bone marrow transplantation.
Bone marrow transplantation 1998;22(11):1115-7.
1998: Shrimati Shetty; Kanjaksha Ghosh; Anil Pathare; Farah Jijina; Dipika Mohanty
Molecular characterization of haemophilia A & B in Indians.
Haemophilia : the official journal of the World Federation of Hemophilia 1998;4(6):802-5.
1998: Shrimati Shetty; Roshan B Colah; Ajit C Gorakshakar; A Bhide; Kanjaksha Ghosh; Anil Pathare; Farah Jijina; Dipika Mohanty
Prenatal diagnosis of haemophilia: a preliminary report.
The National medical journal of India 1998;11(5):218-9.
1998: Kanjaksha Ghosh; Dipika Mohanty; Anil Pathare; Farah Jijina
Recurrent haemoperitoneum in a female patient with type III von Willebrand's disease responded to administration of oral contraceptive.
Haemophilia : the official journal of the World Federation of Hemophilia 1998;4(5):767-8.
1998: Malay B Mukherjee; Reema R Surve; AA Tamankar; Raman R Gangakhedkar; Kanjaksha Ghosh; C Y Lu; R Krishnamoorthy; Roshan B Colah; Dipika Mohanty
The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India.
The Indian journal of medical research 1998;107():178-81.
1998: Shrimati Shetty; Anil Pathare; Kanjaksha Ghosh; Farah Jijina; Dipika Mohanty
Intron 22 inversions in factor VIII gene in Indian hemophiliacs.
Thrombosis and haemostasis 1998;79(4):881.
1998: Kanjaksha Ghosh; Farah Jijina; Anil Pathare; Dipika Mohanty
Surgery in haemophilia: experience from a centre in India.
Haemophilia : the official journal of the World Federation of Hemophilia 1998;4(2):94-7.
1998: Kanjaksha Ghosh; Dileep Yavagal; C Phillips; Farah Jijina; Anil Pathare; Lily Kerketta; Yegneshwar Iyer; Chandrika N Nair; S Shinde; Dipika Mohanty
Ultrastructural, cell culture and karyotype study of bone marrow in a patient with congenital dyserythropoietic anaemia (CDA)-type III presenting with recurrent still-births.
Haematologia 1998;29(1):41-5.
1998: Farah Jijina; Kanjaksha Ghosh; Dileep Yavagal; Anil Pathare; Dipika Mohanty
A patient with congenital dyserythropoietic anaemia type III presenting with stillbirths.
Acta haematologica 1998;99(1):31-3.
1997: Anita H Nadkarni; Kanjaksha Ghosh; D Mohanty; Roshan B Colah
Hemoglobin E and pyrimidine 5' nucleotidase deficiency.
Blood 1997;90(4):1716.
1997: Shrimati Shetty; Kanjaksha Ghosh; Anil Pathare; Roshan B Colah; S Badakare; Dipika Mohanty
Factor VIII and IX gene polymorphisms and carrier analysis in Indian population.
American journal of hematology 1997;54(4):271-5.
1997: M B Mukherjee; Roshan B Colah; Kanjaksha Ghosh; D Mohanty; R Krishnamoorthy
Milder clinical course of sickle cell disease in patients with alpha thalassemia in the Indian subcontinent.
Blood 1997;89(2):732.
1997: K N Jhaveri; Kanjaksha Ghosh; Dipika Mohanty; B D Parmar; R R Surati; H M Camoens; S H Joshi; Yegneshwar Iyer; A Desai; Suresh S Badakere
Autoantibodies, immunoglobulins, complement and circulating immune complexes in acute malaria.
The National medical journal of India 1997;10(1):5-7.
1997: Dipika Mohanty; Kanjaksha Ghosh; S K Nandwani; Shrimati Shetty; C Phillips; S Rizvi; B D Parmar
Fibrinolysis, inhibitors of blood coagulation, and monocyte derived coagulant activity in acute malaria.
American journal of hematology 1997;54(1):23-9.
1996: Kanjaksha Ghosh; S Shetty; D Mohanty
Inherited deficiency of multiple vitamin K-dependent coagulation factors and coagulation inhibitors presenting as hemorrhagic diathesis, mental retardation, and growth retardation.
American journal of hematology 1996;52(1):67.
1996: M Sivakumaran; Kanjaksha Ghosh; Y Zaidi; R M Hutchinson
Osteoporosis and vertebral collapse following low-dose, low molecular weight heparin therapy in a young patient.
Clinical and laboratory haematology 1996;18(1):55-7.
1996: M Sivakumaran; Kanjaksha Ghosh; L Tan; J Revill; R M Hutchinson; J K Wood
Evaluation of the Pall RC100 leucocyte removal filters and the effect of air introduction on its performance.
Haematologia 1996;27(4):211-6.
1996: Kanjaksha Ghosh; R M Hutchinson
Does oxypentifylline reduce the intensity of acute graft-versus-host disease following allogeneic bone marrow transplantation?
Haematologia 1996;28(1):45-51.
1993: M Sivakumaran; R M Hutchinson; J K Wood; J A Revill; Kanjaksha Ghosh; S Myint
Removal of cytomegalovirus (CMV) infected leucocytes from CMV seropositive blood units by bedside blood filtration.
British journal of haematology 1993;85(1):232-4.