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Burjor Bharucha

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Priyanka Arora; Milind Tullu; Mamta N Muranjan; Sheela P Kerkar; K M Girisha; Burjor A Bharucha
Congenital and inherited ophthalmologic abnormalities.
Ramesh C Parmar; Mamta N Muranjan; S Kotvaliwale; Seema Sharma; Burjor A Bharucha
Ring chromosome 12 with variable phenotypic features: clinical report and review of the literature.
Mamta N Muranjan; S Nirmala; Burjor A Bharucha
Carpal-tarsal osteolysis in monozygotic twins with a new finding.

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All Publications

2003: Priyanka Arora; Milind Tullu; Mamta N Muranjan; Sheela P Kerkar; K M Girisha; Burjor A Bharucha
Congenital and inherited ophthalmologic abnormalities.
Indian journal of pediatrics 2003;70(7):549-52.
2003: Ramesh C Parmar; Mamta N Muranjan; S Kotvaliwale; Seema Sharma; Burjor A Bharucha
Ring chromosome 12 with variable phenotypic features: clinical report and review of the literature.
American journal of medical genetics. Part A 2003;117A(3):275-7.
2001: Mamta N Muranjan; S Nirmala; Burjor A Bharucha
Carpal-tarsal osteolysis in monozygotic twins with a new finding.
Clinical dysmorphology 2001;10(4):281-3.
2001: Milind Tullu; P Arora; Ramesh C Parmar; Mamta N Muranjan; Burjor A Bharucha
Ovarian dysgenesis with balanced autosomal translocation.
Journal of postgraduate medicine 2001;47(2):113-5.
2000: Milind Tullu; Mamta N Muranjan; Pratima Kondurkar; Burjor A Bharucha
Krabbe disease--clinical profile.
Indian pediatrics 2000;37(9):939-46.
2000: Mamta N Muranjan; Burjor A Bharucha
Unusual hand malformations with cardiac defects--a variant of heart--hand syndrome IV.
Indian journal of pediatrics 2000;67(5):392-4.
2000: Milind Tullu; Mamta N Muranjan; Vishakha C Kantharia; Ramesh C Parmar; DK Sahu; Sandeep B Bavdekar; Burjor A Bharucha
Neurofibromatosis-Noonan syndrome or LEOPARD Syndrome? A clinical dilemma.
Journal of postgraduate medicine 2000;46(2):98-100.
2000: Milind Tullu; Mamta N Muranjan; S U Save; Chandrahas T Deshmukh; S R Khubchandani; Burjor A Bharucha
Dorfman-Chanarin syndrome: a rare neutral lipid storage disease.
Indian pediatrics 2000;37(1):88-93.
1999: Milind Tullu; Chandrahas T Deshmukh; Pradeep Vaideeswar; Burjor A Bharucha; P K Arora
Mediastinal yolk sac tumor--a rare presentation.
Indian pediatrics 1999;36(12):1259-62.
1999: Milind Tullu; Chandrahas T Deshmukh; S U Save; B K Bhoite; Burjor A Bharucha
Superior sagittal sinus thrombosis: a rare complication of nephrotic syndrome.
Journal of postgraduate medicine 1999;45(4):120-2.
1999: Talib Y Surve; Mamta N Muranjan; Chandrahas T Deshmukh; C S Warke; Burjor A Bharucha
Inflammatory linear verrucous epidermal nevus syndrome with bilateral vertebral artery occlusion.
Indian pediatrics 1999;36(8):820-3.
1999: Milind Tullu; P Arora; Chandrahas T Deshmukh; Mamta N Muranjan; Burjor A Bharucha
Benzathine penicillin induced immune haemolytic anaemia.
Journal of postgraduate medicine 1999;45(2):58-9.
1999: Mamta N Muranjan; Burjor A Bharucha; M V Kirtane; Chandrahas T Deshmukh
Mondini dysplasia of the inner ear with CSF leak-A rare cause of recurrent meningitis.
Indian pediatrics 1999;36(4):401-6.
1999: Mamta N Muranjan; M Gurav; Talib Y Surve; Chandrahas T Deshmukh; Burjor A Bharucha
Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndrome.
Indian journal of pediatrics 1999;66(1):151-4.
1998: Milind Tullu; Mamta N Muranjan; S V Sharma; DK Sahu; S R Swami; Chandrahas T Deshmukh; Burjor A Bharucha
Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
Journal of postgraduate medicine 1998;44(4):101-4.
1996: A S Kher; D R Gahankari; S R Tambwekar; A Doraiswamy; S Iyer; Burjor A Bharucha; R E Rana
Supernumerary limbs: a case report of a rare congenital anomaly.
Annals of plastic surgery 1996;37(5):549-52.
1996: A D Udwadia; S Khambadkone; Burjor A Bharucha; Y Lokhandwala; S F Irani
Familial congenital valvar pulmonary stenosis: autosomal dominant inheritance.
Pediatric cardiology 1996;17(6):407-9.
1996: M Kaur; Madhulika Kabra; A Kher; G Naik; Burjor A Bharucha; IC Verma
Clinical and enzyme studies in Gaucher disease.
Indian pediatrics 1996;33(9):735-8.
1996: S L Iyer; A Duraiswamy; A S Kher; S Joshi; Burjor A Bharucha; S Kanade
Cri du chat syndrome.
Journal of postgraduate medicine 1996;42(3):86-8.
1995: S G Lalwani; A Kher; N Shridhar; Burjor A Bharucha; G G Naik
Mucolipidoses--II: A report of three cases.
Indian journal of pediatrics 1995;62(5):611-4.
1995: G L Gupte; S V Kotvaliwale; J V Mahajan; A S Kher; S P Kanade; Burjor A Bharucha
48 XXXY variant of Klinefelter syndrome.
Indian pediatrics 1995;32(7):798-801.
1995: G L Gupte; A S Kher; S Bansal; Burjor A Bharucha; S P Kanade; S V Sharma
If the iris is absent?
Indian pediatrics 1995;32(6):702-3.
1995: G L Gupte; A S Kher; S M Joshi; Burjor A Bharucha; S P Kanade
Lissencephaly.
Indian pediatrics 1995;32(5):593-6.
1995: G L Gupte; Chandrahas T Deshmukh; Burjor A Bharucha; S F Irani
Klippel-Trenaunay-Weber syndrome with hydrocephalus: an unusual association.
Pediatric neurosurgery 1995;22(6):328-9.
1994: A Chattopadhyay; A M Shah; S M Khambadkone; K M Dixit; Burjor A Bharucha; S F Irani
Joubert syndrome.
Indian pediatrics 1994;31(11):1415-8.
1994: A Duraiswamy; S Iyer; A S Kher; Burjor A Bharucha
Diastrophic dysplasia.
Indian pediatrics 1994;31(11):1403-5.
1994: A S Kher; A Chattopadhyay; S Datta; S Kanade; V K Sreenivasan; Burjor A Bharucha
Familial mosaic Turner syndrome.
Clinical genetics 1994;46(5):382-3.
1994: A S Kher; A Chattopadhyay; A Divekar; K Khambekar; Burjor A Bharucha
Joubert syndrome with polydactyly and optic coloboma in two sibs.
Indian journal of pediatrics 1994;61(6):729-32.
1994: S Alavi; A Kher; Burjor A Bharucha
Schinzel-Giedion syndrome.
Indian pediatrics 1994;31(9):1111-4.
1994: A Chattopadhyay; A S Kher; R M Thamke; Chandrahas T Deshmukh; Burjor A Bharucha
Neurofibromatosis presenting with aqueductal stenosis.
Indian journal of pediatrics 1994;61(5):586-7.
1994: A Kher; S Datta; S Kanade; M Valdya; Burjor A Bharucha
Mixed gonadal dysgenesis with 45, X/46, XX/46, XY mosaicism.
Indian journal of pediatrics 1994;61(4):445-6.
1994: M U Sanklecha; A Kher; G G Naik; Burjor A Bharucha; Prashant Mahajan
Storage disorders presenting like mucopolysaccharidosis.
Indian journal of pediatrics 1994;61(4):367-72.
1994: G L Gupte; A S Kher; S P Kanade; Burjor A Bharucha; S N Sagade
Acrodysostosis with 5 alpha reductase deficiency: an unusual association.
Indian journal of pediatrics 1994;61(3):287-90.
1994: H S Bava; A Kher; A Doraiswamy; A K Malik; Burjor A Bharucha; Jaishree R Kamat
Massive haemoptysis controlled by bronchial artery embolisation: a case report.
The Indian journal of chest diseases & allied sciences 1994;36(1):31-4.
1993: A Kher; M Bhat; K L Ratnam; S Khambadkone; Burjor A Bharucha; S F Irani
Spondylocostal dysostosis.
Indian journal of pediatrics 1993;60(6):813-8.
1993: A Chattopadhyay; A S Kher; A D Udwadia; S V Sharma; Burjor A Bharucha; A D Nicholson
Fraser syndrome.
Journal of postgraduate medicine 1993;39(4):228-30.
1993: S Alavi; A Chakrapani; A Kher; Burjor A Bharucha
The Proteus syndrome.
Journal of postgraduate medicine 1993;39(4):219-21.
1993: S Parikh; Burjor A Bharucha; S Kamdar; Nilima A Kshirsagar
Polymorphonuclear leukocyte functions in children with cyanotic and acyanotic congenital heart disease.
Indian pediatrics 1993;30(7):883-90.
1993: S Alavi; A Kher; A Kumar; Mamta N Muranjan; Burjor A Bharucha
Cohen syndrome.
Indian pediatrics 1993;30(5):678-81.
1993: A S Kher; Burjor A Bharucha; Jaishree R Kamat; P Kurkure
Cystic tuberculosis of bones.
Indian pediatrics 1993;30(5):676-8.
1993: A Khungar; Prashant Mahajan; G Gupte; M Vasundhara; A Kher; Burjor A Bharucha
Pseudoachondroplastic dysplasia.
Journal of postgraduate medicine 1993;39(2):91-3.
1992: N Wadhwa; Burjor A Bharucha; U Chablani; N Contractor
An epidemiological study of febrile seizures with special reference to family history and HLA linkage.
Indian pediatrics 1992;29(12):1479-85.
1992: G Gupte; Prashant Mahajan; V K Shreenivas; A Kher; Burjor A Bharucha
Wildervanck syndrome (cervico-oculo-acoustic syndrome).
Journal of postgraduate medicine 1992;38(4):180-2.
1992: B John; A Chakrapani; M Sanklecha; A S Kher; Burjor A Bharucha; N B Kumta
Melkersson Rosenthal syndrome: oligosymptomatic form.
Indian pediatrics 1992;29(9):1163-5.
1992: A Kher; Burjor A Bharucha; N B Kumta
Wilson's disease: initial worsening of neurologic syndrome with penicillamine therapy.
Indian pediatrics 1992;29(7):927-9.
1992: M Sanklecha; A Kher; Burjor A Bharucha
Asymmetric crying facies: the cardiofacial syndrome.
Journal of postgraduate medicine 1992;38(3):147-8,150.
1992: Prashant Mahajan; A Kher; A Khungar; M Bhat; M Sanklecha; Burjor A Bharucha
MURCS association--a review of 7 cases.
Journal of postgraduate medicine 1992;38(3):109-11.
1991: S Dutta; Burjor A Bharucha; P V Vaidya; S A Khurandal; A S Kher; N B Kumta
Deletion of short-arm of chromosome 20:46 XX, del (20) (p 11) with unusual skeletal features.
Indian journal of pediatrics 1991;58(5):701-8.
1990: Burjor A Bharucha; R P Khubchandani; D A Parikh; P G Vaidya; A Kher; N B Kumta
Proteus syndrome.
Indian pediatrics 1990;27(12):1312-6.
1990: P G Deshpande; S U Wagle; S D Mehta; Burjor A Bharucha; S F Irani
Neonatal osteomyelitis and septic arthritis.
Indian pediatrics 1990;27(5):453-7.
1989: A Parikh; V U Vaidya; Burjor A Bharucha; N B Kumta
Pachyonychia congenita (a case report).
Journal of postgraduate medicine 1989;35(3):189-90.
1989: R P Khubchandani; A P Parikh; V U Vaidya; Burjor A Bharucha; N B Kumta
Unusual bone changes and laboratory features in congenital syphilis.
Indian pediatrics 1989;26(6):603-7.
1989: T Y Kagalwala; Suhas Kallapur; A S Rathore; Burjor A Bharucha; S F Irani; S Y Sane; D A Parikh
Congenital histiocytosis X.
Indian pediatrics 1989;26(3):292-6.
1988: T Y Kagalwala; Burjor A Bharucha; R D Khare; N B Kumta
Diagnostic approach to coarse facies.
Indian journal of pediatrics 1988;55(6):861-70.
1988: T Y Kagalwala; Burjor A Bharucha; N B Kumta; G G Naik
The mucopolysaccharidoses: a study of 48 cases.
Indian journal of pediatrics 1988;55(6):919-25.
1988: U Sundaram; Suhas Kallapur; N B Kumta; Burjor A Bharucha; N F Shah; S S Borwankar
Idiopathic interstitial calcinosis.
Indian pediatrics 1988;25(10):1002-5.
1988: U Sundaram; Burjor A Bharucha; N B Kumta; U Date; S Kallapur
Syndrome myxoma.
Indian pediatrics 1988;25(9):888-91.
1988: R M Joshi; Burjor A Bharucha; N B Kumta
Neurocutaneous diseases--a study of 61 cases.
Indian journal of pediatrics 1988;55(4):617-25.
1988: A Parikh; Burjor A Bharucha; N B Kumta
Caudal regression syndrome.
Indian pediatrics 1988;25(3):299-302.
1988: V U Vaidya; A P Parikh; Burjor A Bharucha; N B Kumta
Langer Giedion syndrome.
Indian pediatrics 1988;25(1):99-101.
1987: T Y Kagalwala; V U Vaidya; R M Joshi; Burjor A Bharucha; N B Kumta
Chondro-ectodermal dysplasia.
Indian pediatrics 1987;24(11):1045-50.
1987: R M Joshi; T Y Kagalwala; Burjor A Bharucha; V U Vaidya; A L Pandya; A P Parikh; N B Kumta
Wilson's disease (a study of 12 cases).
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 1987;6(4):227-8.
1987: V U Vaidya; Burjor A Bharucha; T Y Kagalwala; A L Pandya; N B Kumta
Farber's lipogranulomatosis.
Indian pediatrics 1987;24(8):673-5.
1987: V U Vaidya; S J Sidhva; Burjor A Bharucha; T Y Kagalwala; N B Kumta
MURCS Association. Primary amenorrhea.
Indian pediatrics 1987;24(7):588-92.
1987: T Y Kagalwala; V U Vaidya; Burjor A Bharucha; A L Pandya; N B Kumta
Cavernous hemangiomas of the liver and spleen.
Indian pediatrics 1987;24(5):427-30.
1987: R M Joshi; A L Pandya; Burjor A Bharucha; R Ramakantan; N B Kumta
Acrodysostosis syndrome.
Indian journal of pediatrics 1987;54(2):271-3.
1987: Burjor A Bharucha; T Y Kagalwala; A L Pandya; V U Vaidya; N B Kumta
Cyproheptadine poisoning.
Indian pediatrics 1987;24(2):165-9.
1986: R M Joshi; Burjor A Bharucha; R Ramakantan; N B Kumta
An overview of the congenital malformations of the lower respiratory tract.
The Indian journal of chest diseases & allied sciences 1986;28(1):6-10.
1986: N B Kumta; Burjor A Bharucha; A L Pandya; T Y Kagalwala; V U Vaidya; S M Rane
Menkes steely hair disease.
Indian pediatrics 1986;23(1):64-7.
1985: A Pandya; Burjor A Bharucha; S D Patwardhan; T Y Kagalwalla; N B Kumta
A multiple malformations syndrome with cleft lip and palate and ankyloblepharon filiforme adnatum.
Indian journal of pediatrics 1985;52(419):667-70.
1985: R M Joshi; Burjor A Bharucha; N B Kumta; R Ramakantan
Genetics of congenital dwarfism.
Indian journal of pediatrics 1985;52(418):545-7.
1985: G V Kopikar; R M Joshi; Burjor A Bharucha; N B Kumta
Craniofacial malformations.
Indian pediatrics 1985;22(6):411-4.
1985: R M Joshi; Burjor A Bharucha; N B Kumta; A S Vengsarkar
Limb-heart syndrome.
Indian pediatrics 1985;22(5):355-9.
1985: R M Joshi; Burjor A Bharucha; M D Mohire; N B Kumta
Congenital myasthenia gravis (a case report).
Journal of postgraduate medicine 1985;31(2):109-11.
1985: R M Joshi; M D Mohire; Burjor A Bharucha; N B Kumta; A P Desai; A D Desai
Pompe's disease.
Indian pediatrics 1985;22(4):315-8.
1985: R M Joshi; Burjor A Bharucha; N B Kumta
Congenital limb defects.
Indian pediatrics 1985;22(2):107-12.
1984: Burjor A Bharucha; A S Savliwala; G V Koppikar; G G Naik; N B Kumta
An approach to diagnosis of hepatic glycogenosis.
Indian pediatrics 1984;21(11):855-63.
1984: R M Joshi; Burjor A Bharucha; S D Patwardhan; N B Kumta
Hemangiomatous malformation of thoracic vertebra.
Indian pediatrics 1984;21(11):900-3.
1984: Burjor A Bharucha; G Naik; A S Savliwala; R M Joshi; N B Kumta
Siblings with the Austin variant of metachromatic leukodystrophy multiple sulfatidosis.
Indian journal of pediatrics 1984;51(411):477-80.
1983: Burjor A Bharucha; A S Savliwala; G V Koppikar; N B Kumta
Camptomelic dwarfism syndrome (a case report).
Journal of postgraduate medicine 1983;29(4):268-70.
1983: Burjor A Bharucha; A S Savliwala; G V Koppikar; N B Kumta
Siblings with Larsen's syndrome.
Indian pediatrics 1983;20(5):375-7.
1983: Burjor A Bharucha; U M Agarwal; A S Savliwala; R Kolluri; N B Kumta
Trisomy 18: Edward's syndrome (a case report of 3 cases).
Journal of postgraduate medicine 1983;29(2):129-32.
1983: A S Savliwala; G Naik; Burjor A Bharucha; R D Khare; N B Kumta
Sandhoff's disease GM2 gangliosidosis: Type-2.
Indian pediatrics 1983;20(2):134-7.