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Aytemiz Gürgey

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Müge Gökçe; Hayriye Gülşen; Fatma Gümrük; Ozge Başaran; Nesrin Beşbaş; Mualla Cetin; Sule Unal; Aytemiz Gürgey
A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis.
Didem Armangil; Hamza Okur; Murat Yurdakök; Aytemiz Gürgey
Plasminogen activator inhibitor I 4G/5G polymorphism in neonatal respiratory distress syndrome.
A Bülent Cengiz; Oge Cultu-Kantaroğlu; Gülten Seçmeer; Mehmet Ceyhan; Ates Kara; Aytemiz Gürgey
Infectious mononucleosis in Turkish children.

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2012: Müge Gökçe; Hayriye Gülşen; Fatma Gümrük; Ozge Başaran; Nesrin Beşbaş; Mualla Cetin; Sule Unal; Aytemiz Gürgey
A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis.
The Turkish journal of pediatrics 2012;54(1):61-3.
2011: Didem Armangil; Hamza Okur; Murat Yurdakök; Aytemiz Gürgey
Plasminogen activator inhibitor I 4G/5G polymorphism in neonatal respiratory distress syndrome.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2011;17(4):352-7.
2010: A Bülent Cengiz; Oge Cultu-Kantaroğlu; Gülten Seçmeer; Mehmet Ceyhan; Ates Kara; Aytemiz Gürgey
Infectious mononucleosis in Turkish children.
The Turkish journal of pediatrics 2010;52(3):245-54.
2009: Ercan Sivasli; Ozlem Tekşam; Mithat Haliloğlu; Safak Güçer; Diclehan Orhan; Aytemiz Gürgey; Gülsevin Tekinalp
Hydrops fetalis associated with chorioangioma and thrombosis of umbilical vein.
The Turkish journal of pediatrics 2009;51(5):515-8.
2009: Gülten Türkkani-Asal; Yasemin Alanay; Tuba Turul-Ozgür; Martin Zenker; Christian Thiel; Anita Rauch; Sule Unal; Aytemiz Gürgey; Ilhan Tezcan
Mild clinical phenotype and subtle radiographic findings in an infant with cartilage-hair hypoplasia.
The Turkish journal of pediatrics 2009;51(5):493-6.
2009: Erkan Demirkaya; Hasan Fatih Cakmakli; Safak Güçer; Nuray Aktay-Ayaz; Aytemiz Gürgey; Seza Ozen
Purpura fulminans as the presenting manifestation in a patient with juvenile SLE.
The Turkish journal of pediatrics 2009;51(4):378-80.
2009: Tiraje Celkan; Su Gülsün Berrak; Elif Kazanci; Emel Ozyürek; Sule Unal; Canan Uçar; Sebnem Yilmaz; Aytemiz Gürgey
Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.
The Turkish journal of pediatrics 2009;51(3):207-13.
2008: Rezan Topaloğlu; Anne S Lebre; Erkan Demirkaya; Bariş Kuşkonmaz; Turgay Coşkun; Diclehan Orhan; Aytemiz Gürgey; Fatma Gümrük
Two new cases with Pearson syndrome and review of Hacettepe experience.
The Turkish journal of pediatrics 2008;50(6):572-6.
2008: AnnaCarin Horne; Kim Göransdotter Ramme; Eva Rudd; Chengyun Zheng; Yasser Wali; Zakia Al Lamki; Aytemiz Gürgey; Nevin Yalman; Magnus Nordenskjöld; Jan-Inge Henter
Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
British journal of haematology 2008;143(1):75-83.
2008: Yusuf Bayraktar; Ozgur Harmanci; Yahya Büyükasik; Ali Ibrahim Shorbagi; Aysegul Hasegeli Sungur; Cemaliye Akyerli Boylu; Aytemiz Gürgey; Ferhun Balkanci
JAK2V617F mutation in patients with portal vein thrombosis.
Digestive diseases and sciences 2008;53(10):2778-83.
2008: Eva Rudd; Y T Bryceson; Chengyun Zheng; Josefine Edner; S M Wood; K Ramme; S Gavhed; Aytemiz Gürgey; M Hellebostad; A G Bechensteen; Hans-Gustaf Ljunggren; Bengt Fadeel; Magnus Nordenskjöld; Jan-Inge Henter
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
Journal of medical genetics 2008;45(3):134-41.
2008: Betul Tavil; Gülten Seçmeer; Hasan Ozen; A Bülent Cengiz; Sule Unal; Aytemiz Gürgey
Foamy histiocytes in a patient with visceral leishmaniasis after treatment with liposomal amphotericin B.
The Turkish journal of pediatrics 2008;50(1):67-9.
2007: Emel Ozyurek; Gunay Balta; Aydan Degerliyurt; Hülya Parlak; Sabiha Aysun; Aytemiz Gürgey
Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2007;13(2):154-60.
2006: Emel Ozyürek; Koray Ergünay; Baris Kuskonmaz; Sule Unal; Mualla Cetin; Semsettin Ustaçelebi; Aytemiz Gürgey; Fatma Gümrük
Transfusion-transmitted virus prevalence in Turkish patients with thalassemia.
Pediatric hematology and oncology 2006;23(4):347-53.
2006: Eva Rudd; K Göransdotter Ericson; Chengyun Zheng; Z Uysal; A Ozkan; Aytemiz Gürgey; B Fadeel; M Nordenskjöld; Jan-Inge Henter
Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.
Journal of medical genetics 2006;43(4):e14.
2006: Baris Kuskonmaz; Ates Kara; Maide Ozen; A Bülent Cengiz; Metehan Ozen; Gülten Seçmeer; Aytemiz Gürgey
Micrococcus sedentarius bacteraemia presenting with haemophagocytic syndrome in previously healthy boy.
Scandinavian journal of infectious diseases 2006;38(2):146-8.
2005: Aytemiz Gürgey; Selin Aytac; Güler Kanra; Gulten Secmeer; Mehmet Ceyhan; Cigdem Altay
Outcome in children with purpura fulminans: report on 16 patients.
American journal of hematology 2005;80(1):20-5.
2005: Sule Unal; Ali Varan; Bilgehan Yalçin; Münevver Büyükpamukçu; Aytemiz Gürgey
Evaluation of thrombotic children with malignancy.
Annals of hematology 2005;84(6):395-9.
2004: Hale Oren; Omer Devecioğlu; Mehmet Ertem; Canan Vergin; Kaan Kavakli; Adalet Meral; Duran Canatan; Hayri Toksoy; Inci Yildiz; Unsal Ozgen; Haldun Oniz; Emin Kürekçi; Aytemiz Gürgey
Analysis of pediatric thrombotic patients in Turkey.
Pediatric hematology and oncology 2004;21(7):573-83.
2004: M Mert Sözen; Cagatay Karaaslan; Reyhan Oner; Fatma Gümrük; M A Ozdemir; Cigdem Altay; Aytemiz Gürgey; Cihan Oner
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family.
American journal of hematology 2004;76(4):378-82.
2004: Nilgün Sayinalp; I C Haznedaroğlu; Salih Aksu; Y Büyükaşik; Hakan Göker; Hülya Parlak; Osman Ozcebe; Serafettin Kirazli; Semra V Dündar; Aytemiz Gürgey
The predictability of factor V Leiden (FV:Q(506)) gene mutation via clotting-based diagnosis of activated protein C resistance.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2004;10(3):265-70.
2004: Gülten Seçmeer; Hale Sakalli; Faysal Gök; Seza Ozen; Ates Kara; A Bülent Cengiz; Mehmet Ceyhan; Aytemiz Gürgey; Safiye Gögüs; Güler Kanra
Fatal cytophagic histiocytic panniculitis.
Pediatric dermatology 2004;21(3):246-9.
2004: Hayri Toksöz; Sule Unal; Serafettin Kirazli; Aytemiz Gürgey
The effect of short course high dose methylprednisolon therapy on fibrinogen level in children with acute lymphoblastic leukemia. A preliminary study.
Leukemia research 2004;28(5):533-5.
2004: Nuray Oksüz Kanbur; Orhan Derman; Tezer Kutluk; Aytemiz Gürgey
Coagulation disorders as the cause of menorrhagia in adolescents.
International journal of adolescent medicine and health 2004;16(2):183-5.
2004: Aytemiz Gürgey; Sevgi Yetgin; Mualla Cetin; Fatma Gümrük; Ayfer Tuncer; Ergül Tunçbilek; Gönül Hiçsönmez
Acute lymphoblastic leukemia in infants.
The Turkish journal of pediatrics 2004;46(2):115-9.
2003: Kudret Cağlar; Ahmet Cetinkaya; Selin Aytaç; Fatma Gümrük; Aytemiz Gürgey
Use of recombinant factor VIIa for bleeding in children with Glanzmann thrombasthenia.
Pediatric hematology and oncology 2003;20(6):435-8.
2003: Esra Birben; Cihan Oner; Reyhan Oner; Cigdem Altay; Aytemiz Gürgey
Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients.
European journal of haematology 2003;71(1):39-43.
2003: Aytemiz Gürgey; S Göğüş; Emel Ozyürek; Deniz Aslan; Fatma Gümrük; Mualla Cetin; Aysel Yüce; Mehmet Ceyhan; Gülten Seçmeer; Sevgi Yetgin; Gönül Hiçsönmez
Primary hemophagocytic lymphohistiocytosis in Turkish children.
Pediatric hematology and oncology 2003;20(5):367-71.
2003: Sensin Hasçelik; Dilek Yalnizoğlu; Gülden Kafali; Alpay Celiker; Aysenur Cila; Meral Topçu; Aytemiz Gürgey
Stroke owing to noncompaction of myocardium.
Journal of child neurology 2003;18(6):437-9.
2003: Gönül Hiçsönmez; Mualla Cetin; Hamza Okur; Esra Erdemli; Aytemiz Gürgey
The potential effect of short-course high-dose steroid on the maturation and apoptosis of leukemic cells in a child with acute megakaryoblastic leukemia.
Leukemia & lymphoma 2003;44(6):1037-42.
2003: Emel Ozyürek; Nesrin Beşbaş; Deniz Aslan; Aytemiz Gürgey
Trauma as a risk factor for thrombosis in children: a report of three cases.
The Turkish journal of pediatrics 2003;45(2):167-9.
2003: Sevgi Yetgin; Murat Tuncer; Mualla Cetin; Fatma Gümrük; Idil Yenicesu; Bahattin Tunç; Ahmet F Oner; Hayri Toksoy; Ahmet Koç; Deniz Aslan; Emel Ozyürek; Lale Olcay; Lale Atahan; Ergül Tunçbilek; Aytemiz Gürgey
Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up.
Leukemia 2003;17(2):328-33.
2003: Ummiye Venus Onay; Kaan Kavakli; Yurdanur Kilinç; Aytemiz Gürgey; Gülten Aktuğlu; Sabri KEMAHLI; Ugur Ozbek; S Hande Cağlayan
Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations.
British journal of haematology 2003;120(4):656-9.
2003: Kim Göransdotter Ericson; Bengt Fadeel; Mats Andersson; Gudmundur H Gudmundsson; Aytemiz Gürgey; Nevin Yalman; Gritta Janka; Magnus Nordenskjöld; Jan-Inge Henter
Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
Human genetics 2003;112(1):98-9.
2002: Ozden Sanal; Fügen Ersoy; Ilhan Tezcan; Ayse Metin; Leman Yel; Gaël Ménasché; Aytemiz Gürgey; Izzet Berkel; Geneviève de Saint Basile
Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.
Journal of clinical immunology 2002;22(4):237-43.
2002: Esra Birben; Reyhan Oner; Cihan Oner; Fatma Gümrük; Cigdem Altay; Aytemiz Gürgey
Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
British journal of haematology 2002;118(1):278-81.
2002: Deniz Aslan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Importance of RDW value in differential diagnosis of hypochrome anemias.
American journal of hematology 2002;69(1):31-3.
2002: Zekai Avci; Tuba Turul; Ferhat Catal; Seref Olgar; Ali Baykan; Ozlem Tekfam; Aytemiz Gürgey
Thrombocytopenia and emperipolesis in a patient with hepatitis a infection.
Pediatric hematology and oncology 2002;19(1):67-70.
2002: Reyhan Oner; Ceren Acar; Cihan Oner; Idil Yenicesu; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Pediatric hematology and oncology 2002;19(1):39-44.
2001: Gülsevin Tekinalp; S.Umit Sarici; A S Erdinç; S Gögüş; Sevim Balci; Aytemiz Gürgey
Lethal hydrops fetalis due to congenital dyserythropoietic anemia in a newborn: association of a new skeletal abnormality.
Pediatric hematology and oncology 2001;18(8):537-42.
2001: Idil Yenicesu; Duygu Uçkan; Mualla Cetin; Ayfer Tuncer; Ilhan Tezcan; Aytemiz Gürgey
Evaluation of coagulation in pediatric bone marrow transplantation patients.
Pediatric transplantation 2001;5(6):430-3.
2001: Esra Birben; Cihan Oner; Reyhan Oner; Hatice Mergen; Akif Yesilipek; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
Hemoglobin 2001;25(4):441-5.
2001: Esra Birben; Reyhan Oner; Cihan Oner; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patient.
Hemoglobin 2001;25(4):409-15.
2001: Reyhan Oner; Cihan Oner; Esra Birben; M Mert Sözen; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap site.
British journal of haematology 2001;115(1):90-4.
2001: A A Timur; Aytemiz Gürgey; Gülten Aktuglu; Kaan Kavakli; Duran Canatan; K Olek; Suat Caglayan
Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations.
Haemophilia : the official journal of the World Federation of Hemophilia 2001;7(5):475-81.
2001: H S Kalkanoğlu; T Coşkun; S D Aydoğdu; Aysegul Tokatli; Aytemiz Gürgey
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.
Journal of inherited metabolic disease 2001;24(3):367-9.
2001: K Göransdotter Ericson; Bengt Fadeel; S Nilsson-Ardnor; Cilla Söderhäll; A Samuelsson; Gritta Janka; M Schneider; Aytemiz Gürgey; Nevin Yalman; T Révész; R Maarten Egeler; K Jahnukainen; I Storm-Mathiesen; A Haraldsson ; J Poole; Geneviève de Saint Basile; Magnus Nordenskjöld; Jan-Inge Henter
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
American journal of human genetics 2001;68(3):590-7.
2000: Idil Yenicesu; C Sanli; Aytemiz Gürgey
Idiopathic thrombocytopenic purpura in acute lymphocytic leukemia.
Pediatric hematology and oncology 2000;17(8):719-20.
2000: D Aliefendioğlu; Deniz Aslan; Gülsevin Tekinalp; Aytemiz Gürgey
Pseudomonas sepsis with neutrophagocytosis in a premature newborn.
The Turkish journal of pediatrics 2000;42(4):328-30.
2000: Reyhan Oner; Esra Birben; Ceren Acar; Cihan Oner; Ates Kara; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Hemoglobin 2000;24(3):195-201.
2000: F Cahit Tanyel; Turgay Ocal; Ferhun Balkanci; Saruhan Cekirge; Mehmet Emin Senocak; Nebil Büyükpamukçu; Aytemiz Gürgey
The factor V Leiden mutation: a possible contributor to the hepatic artery thrombosis encountered after liver transplantation in a child.
Journal of pediatric surgery 2000;35(4):607-9.
2000: Duygu Uçkan; Gönül Hiçsönmez; Sevgi Yetgin; Aytemiz Gürgey; Mualla Cetin; E Karaağaoğlu; Hamza Okur; Ayfer Tuncer
CD34/CD117 co-expression in childhood acute leukemia.
Leukemia research 2000;24(3):201-6.
2000: Reyhan Oner; Fatma Gümrük; Ceren Acar; Cihan Oner; Aytemiz Gürgey; Cigdem Altay
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Haematologica 2000;85(3):320-1.
2000: Fatma Gümrük; Hatice Mergen; Reyhan Oner; Osman Ozcebe; Nilgün Sayinalp; Cihan Oner; Aytemiz Gürgey; Cigdem Altay
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Hemoglobin 2000;24(1):23-9.
2000: Reyhan Celiker; Yesim Gökçe Kutsal; B Oy; O Onur; Aytemiz Gürgey
Depression in children with hemophilic arthropathy and poliomyelitis: a preliminary report.
The Turkish journal of pediatrics 2000;42(1):27-30.
2000: Türker Egesel; Yahya Büyükasik; Semra V Dündar; Aytemiz Gürgey; Serafettin Kirazli; Yusuf Bayraktar
The role of natural anticoagulant deficiencies and factor V Leiden in the development of idiopathic portal vein thrombosis.
Journal of clinical gastroenterology 2000;30(1):66-71.
1999: Defne Kalayci; Aytemiz Gürgey; Dilek Güven; Hülya Parlak; Hikmet Hasiripi
Factor V Leiden and prothrombin 20210 A mutations in patients with central and branch retinal vein occlusion.
Acta ophthalmologica Scandinavica 1999;77(6):622-4.
1999: Ahmet Koç; Ali Varan; Münevver Büyükpamukçu; Aytemiz Gürgey
A case of hemophilia A associated with Hodgkin's disease.
The Turkish journal of pediatrics 1999;41(4):517-20.
1999: Aytemiz Gürgey; Idil Yenicesu; T Kanra; Sinasi Ozsoylu; Cigdem Altay; Gönül Hiçsönmez; Sevgi Yetgin; Murat Tuncer; Fatma Gümrük; Mualla Cetin
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 cases.
The Turkish journal of pediatrics 1999;41(4):467-71.
1999: Nilgün Sayinalp; Osman Ozcebe; Serafettin Kirazli; R Doğan; Semra V Dündar; Aytemiz Gürgey
Paget-Schroetter syndrome associated with FV:Q506 and prothrombin 20210A--a case report.
Angiology 1999;50(8):689-92.
1999: Ahmet F Oner; Aytemiz Gürgey; Hamza Okur; Serafettin Kirazli; Fatma Gümrük; Cigdem Altay
Changes of hemostatic factors in patients with hemoglobinopathies.
The Turkish journal of pediatrics 1999;41(3):323-7.
1999: Figen Gürakan; Aytemiz Gürgey; A Bakkaloğlu; Nurten Koçak
Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome.
Journal of pediatric gastroenterology and nutrition 1999;28(5):516-7.
1999: Gunay Balta; Aytemiz Gürgey
Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
The Turkish journal of pediatrics 1999;41(2):197-9.
1999: Ahmet F Oner; Aytemiz Gürgey; Serafettin Kirazli; Hamza Okur; Bahattin Tunç
Changes of hemostatic factors in children with acute lymphoblastic leukemia receiving combined chemotherapy including high dose methylprednisolone and L-asparaginase.
Leukemia & lymphoma 1999;33(3-4):361-4.
1998: Aytemiz Gürgey; G Hicsönmez; Hülya Parlak; Gunay Balta; A Celiker
Prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis.
American journal of hematology 1998;59(2):179-80.
1998: Lale Olcay; Aytekin Besim; Mehmet Emin Senocak; Ayhan Göçmen; Münevver Büyükpamukçu; Gülsev Kale; Mualla Cetin; Aytemiz Gürgey
Hydatid cyst mimicking pulmonary hematoma in a patient with hemophilia A.
The Turkish journal of pediatrics 1998;40(3):425-9.
1998: Sevgi Yetgin; Aytemiz Gürgey; Ayfer Tuncer; Mualla Cetin; Namik Ozbek; T Sayli; Elif Güler; Ates Kara; Lale Olcay; F Duru; Fatma Gümrük; Lale Atahan; Ergül Tunçbilek
A comparison of the effect of high-dose methylprednisolone with conventional-dose prednisolone in acute lymphoblastic leukemia patients with randomization.
Leukemia research 1998;22(6):485-93.
1998: Cihan Oner; Reyhan Oner; H Balkan; Fatma Gümrük; Aytemiz Gürgey
Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha].
Hemoglobin 1998;22(3):273-6.
1998: Cigdem Altay; Cihan Oner; Reyhan Oner; Fatma Gümrük; Hatice Mergen; Aytemiz Gürgey
Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)0-thalassemia traits.
Human heredity 1998;48(3):121-5.
1998: Cihan Oner; Reyhan Oner; Esra Birben; H Balkan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.
Hemoglobin 1998;22(2):157-60.
1998: Ahmet F Oner; Aytemiz Gürgey; A Gürler; Lütfiye Mesci
Factor V Leiden mutation in patients with Behçet's disease.
The Journal of rheumatology 1998;25(3):496-8.
1998: Aytemiz Gürgey; A Gurler; Ahmet F Oner; Lütfiye Mesci; Serafettin Kirazli
Thrombomodulin levels in Behçet's disease with and without the factor V Leiden mutation.
Clinical rheumatology 1998;17(3):186-8.
1998: Cansin Saçkesen; Gülten Seçmeer; Aytemiz Gürgey; Güler Kanra; Z Ecevit; Mehmet Ceyhan; Almila Bulun; Ates Kara; O Türkmen; Hülya Parlak
Homozygous Factor V Leiden mutation in a child with meningococcal purpura fulminans.
The Pediatric infectious disease journal 1998;17(1):87.
1997: Lale Olcay; Aytemiz Gürgey; H Topaloglu; S Altay; Hülya Parlak; M Murat Firat
Cerebral infarct associated with factor V Leiden mutation in a boy with hemophilia A.
American journal of hematology 1997;56(3):189-90.
1997: Mualla Cetin; Aytemiz Gürgey; Fatma Gümrük; Cigdem Altay
Serum erythropoietin in children with iron deficiency anemia.
The Turkish journal of pediatrics 1997;39(4):459-64.
1997: Sevgi Yetgin; Lale Olcay; Sinasi Ozsoylu; Gönül Hiçsönmez; Aytemiz Gürgey; Ayfer Tuncer
Retrospective analysis of 78 children with chronic idiopathic thrombocytopenic purpura: follow-up from 1976 to 1996.
Pediatric hematology and oncology 1997;14(5):399-412.
1997: Aytemiz Gürgey; M Büyükpamukcu; C Baskut; Bilgehan Yalcin; S Gögüş
Portal vein thrombosis in association with factor V Leiden mutation in a patient with hepatocellular carcinoma.
Medical and pediatric oncology 1997;29(3):224-5.
1997: Aytemiz Gürgey; S Göğüş; Umit Saatçi; N Bilginturan; Nursen Yordam; T Coşkun; Süheyla Ozkutlu; N Sahin
Leprechaunism in two Turkish patients.
The Turkish journal of pediatrics 1997;39(3):387-93.
1997: Aytemiz Gürgey; Lütfiye Mesci
The prevalence of factor V Leiden (1691 G-->A) mutation in Turkey.
The Turkish journal of pediatrics 1997;39(3):313-5.
1997: Cigdem Altay; Cihan Oner; Reyhan Oner; Lütfiye Mesci; H Balkan; Sukru Tuzmen; A N Başak; Fatma Gümrük; Aytemiz Gürgey
Genotype-phenotype analysis in HbS-beta-thalassemia.
Human heredity 1997;47(3):161-4.
1997: Aytemiz Gürgey; H Balkan; G Irken; Fatma Gümrük; S Altay; A Kalaycioğlu; Cihan Oner; Reyhan Oner
Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutation.
The Turkish journal of pediatrics 1997;39(2):253-7.
1997: Cihan Oner; Reyhan Oner; H Balkan; Aytemiz Gürgey; Atilla Yalçin; Ferit Avcu; Cigdem Altay
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
British journal of haematology 1997;96(2):229-34.
1997: S H Cağlayan; Y Gökmen; G Aktuğlu; Aytemiz Gürgey; S S Sommer
Mutations associated with hemophilia B in Turkish patients.
Human mutation 1997;10(1):76-9.
1997: Reyhan Celiker; Lale Olcay; A Kara; Aytemiz Gürgey
Clinical and radiological assessment of haemophilic arthropathy in children.
Clinical rheumatology 1997;16(1):109-10.
1997: Cihan Oner; Aytemiz Gürgey; Reyhan Oner; H Balkan; Fatma Gümrük; E Baysal; Cigdem Altay
The molecular basis of Hb H disease in Turkey.
Hemoglobin 1997;21(1):41-51.
1997: Gönül Hiçsönmez; Fatma Gümrük; P V Zamani; Murat Tuncer; Sevgi Yetgin; Aytemiz Gürgey; Lale Atahan; S Ozsoylu
High-dose methylprednisolone for children with acute lymphoblastic leukemia and unfavorable presenting features.
European journal of haematology 1997;58(1):26-31.
1996: T Kanra; Gülsen Erdem; Gülsevin Tekinalp; Aytemiz Gürgey; Sule Yigit; D Dogru
Further hemolytic disease of the newborn caused by anti-M.
American journal of hematology 1996;53(4):280-1.
1996: Gülsevin Tekinalp; Olcay Oran; B Gürakan; M Saraçel; Gülsen Erdem; Murat Yurdakök; Aytemiz Gürgey
Relationship between maternal and neonatal iron stores.
The Turkish journal of pediatrics 1996;38(4):439-45.
1996: Aytemiz Gürgey; Imran Ozalp; A Rötig; T Coşkun; Gülsevin Tekinalp; Gülsen Erdem; Z Akeören; Melda Caglar; Aysin Bakkaloglu
A case of Pearson syndrome associated with multiple renal cysts.
Pediatric nephrology (Berlin, Germany) 1996;10(5):637-8.
1996: NS Smetanina; Cihan Oner; E Baysal; Reyhan Oner; G Bozkurt; Cigdem Altay; Aytemiz Gürgey; Adekunle Adekile; LH Gu; TH Huisman
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.
Biochimica et biophysica acta 1996;1316(3):176-82.
1996: Cigdem Altay; Aytemiz Gürgey; A Nazli Basak; Ghazi Tadmouri; T Schroeder-Kurt
Fanconi aplastic anemia associated with beta-thalassemia trait.
American journal of hematology 1996;52(3):239-40.
1996: Lale Olcay; Sema Ozer; Aytemiz Gürgey; Muhsin Saraçlar; Sencan Ozme; Arman Bilgiç; Süheyla Ozkutlu; Alpay Celiker
Parameters of iron deficiency in children with cyanotic congenital heart disease.
Pediatric cardiology 1996;17(3):150-4.
1996: Aytemiz Gürgey; T Sayli; Ates Kara; Gülsev Kale; I Berkel
Treatment of X-linked lymphoproliferative disease (Duncan disease) with high-dose methylprednisolone and etoposide (VP-16).
The Turkish journal of pediatrics 1996;38(2):217-22.
1996: Aytemiz Gürgey; S Beksaç; E Gümrük; N Cakar; L Mesçi; S Altay; Cihan Oner; Cigdem Altay
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience.
Pediatric hematology and oncology 1996;13(2):163-6.
1996: C Altay; E Yilgör; S Beksac; Aytemiz Gürgey
Premarital screening of hemoglobinopathies: a pilot study in Turkey.
Human heredity 1996;46(2):112-4.
1996: Reyhan Oner; Cihan Oner; Gülsen Erdem; H Balkan; H Ozdağ; M Erkan; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family.
Acta haematologica 1996;96(4):232-6.
1995: Aytemiz Gürgey; Lütfiye Mesci; K Ozerkam; Cihan Oner
Analysis of chimerism by PCR using mutant-specific primers and sequencing of B-gene region after allogenic bone marrow transplantation in sickle cell anemia.
American journal of hematology 1995;50(4):318-9.
1995: Aytemiz Gürgey; Cigdem Altay; LH Gu; J Y Leonova; A Delibalta; Cihan Oner; TH Huisman
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow.
Hemoglobin 1995;19(3-4):165-72.
1995: Mualla Cetin; Ates Kara; Aytemiz Gürgey; Fatma Gümrük; Gülersu Irken; Sevgi Yetgin; Cigdem Altay
Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.
Pediatric hematology and oncology 1995;12(2):153-8.
1995: Cihan Oner; Reyhan Oner; Aytemiz Gürgey; Cigdem Altay
A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta gene.
British journal of haematology 1995;89(2):306-12.
1995: Gönül Hiçsönmez; M Cetin; M A Tuneer; Fatma Gümrük; Namik Ozbek; Ates Kara; Aytemiz Gürgey
High-dose methylprednisolone for remission induction in hypoplastic acute myeloid leukemia.
European journal of haematology 1995;54(2):125-6.
1995: Aytemiz Gürgey; N Bilginturan; Nursen Yordam; S Vidinlisan; C Altay; S S Dişkapi
Anemia associated with diabetes mellitus.
Pediatric hematology and oncology 1995;12(1):83-5.
1994: F Duru; Aytemiz Gürgey
Effect of corticosteroids in hereditary spherocytosis.
Acta paediatrica Japonica; Overseas edition 1994;36(6):666-8.
1994: Atilla Yalçin; Ferit Avcu; Cengiz Beyan; Aytemiz Gürgey; A. Ugur URAL
A case of HB J-Meerut (or Hb J-Birmingham) [alpha 120(H3)Ala-->Glu].
Hemoglobin 1994;18(6):433-5.
1994: N Beşbaş; Seza Ozen; A Bakkaloğlu; Aytemiz Gürgey; T Kanra; Umit Saatçi
Plasma exchange in refractory autoimmune anemia in a child with systemic vasculitis associated with homozygote beta thalassemia.
The Turkish journal of pediatrics 1994;36(4):337-40.
1994: Aytemiz Gürgey; Omer Kalayci; Fatma Gümrük; Mualla Cetin; Cigdem Altay
Convulsion after blood transfusion in four beta-thalassemia intermedia patients.
Pediatric hematology and oncology 1994;11(5):549-52.
1994: Aytemiz Gürgey; Aysel Yüce; Namik Ozbek; Nurten Koçak
Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait.
The Turkish journal of pediatrics 1994;36(3):259-62.
1994: F Duru; Fatma Gümrük; Aytemiz Gürgey
Vacuolated white blood cells in thalassemia major.
The Turkish journal of pediatrics 1994;36(3):255-8.
1994: Dimitar G Efremov; A J Dimovski; E Baysal; Z Ye; Adekunle Adekile; Maria Letícia Ribeiro; G Schiliro; Cigdem Altay; Aytemiz Gürgey; Georgi D Efremov
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
British journal of haematology 1994;86(4):824-30.
1994: Aytemiz Gürgey; Ates Kara; M Tuncer; M Alikaşifoğlu; Ergül Tunçbilek
Acute lymphoblastic leukemia associated with Klinefelter syndrome.
Pediatric hematology and oncology 1994;11(2):227-9.
1994: T R Sayli; A N Başak; Fatma Gümrük; Aytemiz Gürgey; Cigdem Altay
Imerslund-Gräsbeck syndrome coexisting with beta-thalassemia trait.
Pediatric hematology and oncology 1994;11(2):223-5.
1994: A Dursun; A Kubar; A Gokoz; F Duru; Aytemiz Gürgey
Neutral lipid storage disease co-existing with ichthyosiform dermatosis.
European journal of pediatrics 1994;153(3):210-1.
1994: F Duru; Aytemiz Gürgey; Mualla Cetin; T Kanra; Cigdem Altay
Chronic autoimmune hemolytic anemia in children: a report of four patients.
Journal of medicine 1994;25(3-4):231-40.
1994: Mualla Cetin; Sevgi Yetgin; Ates Kara; Ayfer Tuncer; M Günay; Fatma Gümrük; Aytemiz Gürgey
Hyperglycemia, ketoacidosis and other complications of L-asparaginase in children with acute lymphoblastic leukemia.
Journal of medicine 1994;25(3-4):219-29.
1993: M A Cürük; A J Dimovski; E Baysal; LH Gu; Ferdane Kutlar; TP Molchanova; B B Webber; Cigdem Altay; Aytemiz Gürgey; TH Huisman
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
American journal of hematology 1993;44(4):270-5.
1993: Lütfiye Mesci; Aytemiz Gürgey; Cigdem Altay
Recent progress in DNA technology.
The Turkish journal of pediatrics 1993;35(3):239-40.
1993: Aytemiz Gürgey; S Beksaç; Lütfiye Mesci; N Cakar; U Karakaş; Abdullah Kutlar; Cigdem Altay
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
The Turkish journal of pediatrics 1993;35(3):159-62.
1993: T Sayli; A P Cemeroglu; Ayfer Tuncer; Aytemiz Gürgey
Acute lymphoblastic leukemia following optic glioma treated by radiotherapy and surgery.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(3):327-8.
1992: F Duru; Aytemiz Gürgey; G Oztürk; S Yörükan; Cigdem Altay
Homozygosity for dominant form of hereditary spherocytosis.
British journal of haematology 1992;82(3):596-600.
1992: Fatma Gümrük; Aytemiz Gürgey; F Duru; Cigdem Altay
Reevaluation of iron absorption and serum ferritin in beta-thalassemia intermedia.
Pediatric hematology and oncology 1992;9(4):359-63.
1992: A N Başak; H Ozçelik; A Ozer; A Tolun; M Cemalettin Aksoy; L Ağaoğlu; F Ridolfi; L Ulukutlu; N Akar; Aytemiz Gürgey
The molecular basis of beta-thalassemia in Turkey.
Human genetics 1992;89(3):315-8.
1992: Aytemiz Gürgey; A Rötig; Fatma Gümrük; P Cemeroğlu; F Sarialioğlu; Cigdem Altay
Pearson's marrow-pancreas syndrome in 2 Turkish children.
Acta haematologica 1992;87(4):206-9.
1992: A N Başak; A Ozer; H Ozçelik; B Kirdar; Aytemiz Gürgey
A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.
Hemoglobin 1992;16(4):309-12.
1990: Cigdem Altay; Aytemiz Gürgey
Beta-thalassemia intermedia in Turkey.
Annals of the New York Academy of Sciences 1990;612():81-9.
1990: Aytemiz Gürgey; Sinasi Ozsoylu; Gönül Hiçsönmez; Gülersu Irken; Cigdem Altay
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran.
The Turkish journal of pediatrics 1990;32(1):39-41.
1989: Gönül Hiçsönmez; Sinasi Ozsoylu; Aytemiz Gürgey; V P Zamani; Gülersu Irken
High-dose methylprednisolone for remission induction in children with acute nonlymphoblastic leukemia.
European journal of haematology 1989;42(5):498-500.
1989: Sinasi Ozsoylu; Gülersu Irken; Aytemiz Gürgey
High dose intravenous methylprednisolone for Kassabach-Merritt syndrome.
European journal of pediatrics 1989;148(5):403-5.
1988: Gönül Hiçsönmez; Aytemiz Gürgey; V P Zamani; Sevgi Yetgin; C Altay; Sinasi Ozsoylu
Poor prognosis in children with acute nonlymphoblastic leukemia in Turkey.
The American journal of pediatric hematology/oncology 1988;10(3):268-72.
1987: Aytemiz Gürgey; Gönül Hiçsönmez; Sevim Balci; G Ertürk; Gülersu Irken
Leukemias associated with neurofibromatosis in children.
The Turkish journal of pediatrics 1987;29(3):171-6.
1983: S Osman; Aytemiz Gürgey; V P Zamani; C Altay
Changes in serum elements of childhood acute lymphoblastic leukemia before and during therapy.
The Turkish journal of pediatrics 1983;25(4):233-43.
1983: Aytemiz Gürgey; Sinasi Ozsoylu; T Kanra; G Ertürk
A case of autoimmune hemolytic anemia following thrombocytopenia.
The Turkish journal of pediatrics 1983;25(1):63-7.
1982: Gönül Hiçsönmez; Sinasi Ozsoylu; Sevgi Yetgin; V Zamani; Aytemiz Gürgey; I Atahan
Prognosis in 262 Turkish children with acute lymphocytic leukemia.
The Turkish journal of pediatrics 1982;24(3):159-67.