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Aytemiz Gürgey

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Turkey

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Publications

TOP 3
Celkan Tiraje; Berrak Su; Kazanci Elif; Ozyürek Emel; Unal Sule; Uçar Canan; Yilmaz Sebnem; Gürgey Aytemiz
Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.
Topaloglu Rezan; Lebre Anne S; Demirkaya Erkan; Kuskonmaz Baris; Coskun Turgay; Orhan Diclehan; Gürgey Aytemiz; Gümrük Fatma
Two new cases with Pearson syndrome and review of Hacettepe experience.
Bayraktar Yusuf; Harmanci Ozgur; Büyükasik Yahya; Shorbagi Ali Ibrahim; Sungur Aysegul Hasegeli; Boylu Cemaliye Akyerli; Gürgey Aytemiz; Balkanci Ferhun
JAK2V617F mutation in patients with portal vein thrombosis.

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All Publications

2009: Celkan Tiraje; Berrak Su; Kazanci Elif; Ozyürek Emel; Unal Sule; Uçar Canan; Yilmaz Sebnem; Gürgey Aytemiz
Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.
The Turkish journal of pediatrics 2009;51(3):207-13.
2008: Topaloglu Rezan; Lebre Anne S; Demirkaya Erkan; Kuskonmaz Baris; Coskun Turgay; Orhan Diclehan; Gürgey Aytemiz; Gümrük Fatma
Two new cases with Pearson syndrome and review of Hacettepe experience.
The Turkish journal of pediatrics 2008;50(6):572-6.
2008: Bayraktar Yusuf; Harmanci Ozgur; Büyükasik Yahya; Shorbagi Ali Ibrahim; Sungur Aysegul Hasegeli; Boylu Cemaliye Akyerli; Gürgey Aytemiz; Balkanci Ferhun
JAK2V617F mutation in patients with portal vein thrombosis.
Digestive diseases and sciences 2008;53(10):2778-83.
2008: Horne AnnaCarin; Ramme Kim Göransdotter; Rudd Eva; Zheng Chengyun; Wali Yasser; al-Lamki Zakia; Gürgey Aytemiz; Yalman Nevin; Nordenskjöld Magnus; Henter Jan-Inge
Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
British journal of haematology 2008;143(1):75-83.
2008: Rudd E; Bryceson Y T; Zheng C; Edner J; Wood S M; Ramme K; Gavhed S; Gürgey A; Hellebostad M; Bechensteen A G; Ljunggren H-G; Fadeel B; Nordenskjöld M; Henter J-I
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
Journal of medical genetics 2008;45(3):134-41.
2008: Tavil Betül; Seçmeer Gülten; Ozen Hasan; Cengiz Ali Bülent; Unal Sule; Gürgey Aytemiz
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: Ozyurek Emel; Balta Gunay; Degerliyurt Aydan; Parlak Hülya; Aysun Sabiha; Gürgey Aytemiz
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: Ozyürek Emel; Ergünay Koray; Kuskonmaz Baris; Unal Selma; Cetin Mualla; Ustaçelebi Semsettin; Gürgey Aytemiz; Gümrük Fatma
Transfusion-transmitted virus prevalence in Turkish patients with thalassemia.
Pediatric hematology and oncology 2006;23(4):347-53.
2006: Rudd E; Göransdotter Ericson K; Zheng C; Uysal Z; Ozkan A; Gürgey A; Fadeel B; Nordenskjöld M; Henter J-I
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: Kuskonmaz Baris; Kara Ates; Ozen Maide; Cengiz A Bülent; Ozen Metehan; Seçmeer Gülten; Gürgey Aytemiz
Micrococcus sedentarius bacteraemia presenting with haemophagocytic syndrome in previously healthy boy.
Scandinavian journal of infectious diseases 2006;38(2):146-8.
2005: Gürgey Aytemiz; Aytac Selin; Kanra Guler; Secmeer Gulten; Ceyhan Mehmet; Altay Cigdem
Outcome in children with purpura fulminans: report on 16 patients.
American journal of hematology 2005;80(1):20-5.
2005: Unal Selma; Varan Ali; Yalçin Bilgehan; Büyükpamukçu Münevver; Gürgey Aytemiz
Evaluation of thrombotic children with malignancy.
Annals of hematology 2005;84(6):395-9.
2004: Oren Hale; Devecioglu Omer; Ertem Mehmet; Vergin Canan; Kavakli Kaan; Meral Adalet; Canatan Duran; Toksoy Hayri; Yildiz Incï; Kürekç i Emin; Ozgen Unsal; Oniz Haldun; Gürgey Aytemiz
Analysis of pediatric thrombotic patients in Turkey.
Pediatric hematology and oncology 2004;21(7):573-83.
2004: Sözen M; Karaaslan C; Oner R; Gümrük F; Ozdemir M A; Altay C; Gürgey A; Oner C
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: Sayinalp N; Haznedaroglu I C; Aksu S; Büyükasik Y; Göker H; Parlak H; Ozcebe O I; Kirazli S; Dündar S V; Gürgey A
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: Seçmeer Gülten; Sakalli Hale; Gök Faysal; Ozen Seza; Kara Ates; Cengiz Ali Bülent; Ceyhan Mehmet; Gürgey Aytemiz; Gögüs Safiye; Kanra Güler
Fatal cytophagic histiocytic panniculitis.
Pediatric dermatology 2004;21(3):246-9.
2004: Toksöz Hayri; Unal Selma; Kirazli Serafettin; Gürgey Aytemiz
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: Kanbur Nuray Oksüz; Derman Orhan; Kutluk Tezer; Gürgey Aytemiz
Coagulation disorders as the cause of menorrhagia in adolescents.
International journal of adolescent medicine and health 2004;16(2):183-5.
2004: Gürgey Aytemiz; Yetgin Sevgi; Cetin Mualla; Gümrük Fatma; Tuncer A Murat; Tunçbilek Ergül; Hiçsönmez Gönül
Acute lymphoblastic leukemia in infants.
The Turkish journal of pediatrics 2004;46(2):115-9.
2003: Caglar Kudret; Cetinkaya Ahmet; Aytaç Selin; Gümrük Fatma; Gürgey Aytemiz
Use of recombinant factor VIIa for bleeding in children with Glanzmann thrombasthenia.
Pediatric hematology and oncology 2003;20(6):435-8.
2003: Birben Esra; Oner Cihan; Oner Reyhan; Altay Cigdem; Gürgey Aytemiz
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: Gürgey A; Gögüs S; Ozyürek E; Aslan D; Gümrük F; Cetin M; Yüce A; Ceyhan M; Seçmeer G; Yetgin S; Hiçsönmez G
Primary hemophagocytic lymphohistiocytosis in Turkish children.
Pediatric hematology and oncology 2003;20(5):367-71.
2003: Hasçelik Sensin; Yalnizoglu Dilek; Kafali Gülden; Celiker Alpay; Cila Aysenur; Topçu Meral; Gürgey Aytemiz
Stroke owing to noncompaction of myocardium.
Journal of child neurology 2003;18(6):437-9.
2003: Hiçsönmez Gönül; Cetin Mualla; Okur Hamza; Erdemli Esra; Gürgey Aytemiz
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: Ozyürek Emel; Besbas Nesrin; Aslan Deniz; Gürgey Aytemiz
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: Yetgin S; Tuncer M A; Cetin M; Gümrük F; Yenicesu I; Tunç B; Oner A F; Toksoy H; Koç A; Aslan D; Ozyürek E; Olcay L; Atahan L; Tunçbilek E; Gürgey A
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2003;17(2):328-33.
2003: Onay U Venüs; Kavakli Kaan; Kilinç Yurdanur; Gürgey Aytemiz; Aktuglu Gülten; Kemahli Sabri; Ozbek Ugur; Caglayan S Hande
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: Ericson Kim Göransdotter; Fadeel Bengt; Andersson Mats; Gudmundsson Gudmundur H; Gürgey Aytemiz; Yalman Nevin; Janka Gritta; Nordenskjöld Magnus; Henter Jan-Inge
Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis.
Human genetics 2003;112(1):98-9.
2002: Sanal Ozden; Ersoy Fúgen; Tezcan Ilhan; Metin Ayse; Yel Leman; Ménasché Gaël; Gürgey Aytemiz; Berkel Izzet; de Saint Basile Geneviève
Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.
Journal of clinical immunology 2002;22(4):237-43.
2002: Birben Esra; Oner Reyhan; Oner Cihan; Gümrük Fatma; Altay Cigdem; Gürgey Aytemiz
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: Aslan D; Gümrük F; Gürgey A; Altay C
Importance of RDW value in differential diagnosis of hypochrome anemias.
American journal of hematology 2002;69(1):31-3.
2002: Avci Zekai; Turul Tuba; Catal Ferhat; Olgar Seref; Baykan Ali; Tekfam Ozlem; Gürgey A
Thrombocytopenia and emperipolesis in a patient with hepatitis a infection.
Pediatric hematology and oncology 2002;19(1):67-70.
2002: Oner R; Acar C; Oner C; Yenicesu I; Gümrük F; Gürgey A; Altay C
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: Tekinalp G; Sarici S U; Erdinç A S; Gögüs S; Balci S; Gürgey A
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: Yenicesu I; Uçkan D; Cetin M; Tuncer A M; Tezcan I; Gürgey A
Evaluation of coagulation in pediatric bone marrow transplantation patients.
Pediatric transplantation 2001;5(6):430-3.
2001: Birben E; Oner C; Oner R; Mergen H; Yesilipek A; Gümrük F; Gürgey A; Altay C
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
Hemoglobin 2001;25(4):441-5.
2001: Birben E; Oner R; Oner C; Gümrük F; Gürgey A; Altay C
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patient.
Hemoglobin 2001;25(4):409-15.
2001: Oner R; Oner C; Birben E; Sözen M; Gümrük F; Gürgey A; Altay C
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: Timur A A; Gürgey A; Aktuglu G; Kavakli K; Canatan D; Olek K; Caglayan S H
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: Kalkanoglu H S; Coskun T; Aydogdu S D; Tokatli A; Gürgey A
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.
Journal of inherited metabolic disease 2001;24(3):367-9.
2001: Göransdotter Ericson K; Fadeel B; Nilsson-Ardnor S; Söderhäll C; Samuelsson A; Janka G; Schneider M; Gürgey A; Yalman N; Révész T; Egeler R; Jahnukainen K; Storm-Mathiesen I; Haraldsson A; Poole J; de Saint Basile G; Nordenskjöld M; Henter J
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
American journal of human genetics 2001;68(3):590-7.
2000: Yenicesu I; Sanli C; Gürgey A
Idiopathic thrombocytopenic purpura in acute lymphocytic leukemia.
Pediatric hematology and oncology 2000;17(8):719-20.
2000: Aliefendioglu D; Aslan D; Tekinalp G; Gürgey A
Pseudomonas sepsis with neutrophagocytosis in a premature newborn.
The Turkish journal of pediatrics 2000;42(4):328-30.
2000: Oner R; Birben E; Acar C; Oner C; Kara A; Gümrük F; Gürgey A; Altay C
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Hemoglobin 2000;24(3):195-201.
2000: Tanyel F C; Ocal T; Balkanci F; Cekirge S; Senocak M E; Büyükpamukçu N; Gürgey A
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: Uçkan D; Hiçsönmez G; Yetgin S; Gürgey A; Cetin M; Karaagaoglu E; Okur H; Tuncer A M
CD34/CD117 co-expression in childhood acute leukemia.
Leukemia research 2000;24(3):201-6.
2000: Oner R; Gümrük F; Acar C; Oner C; Gürgey A; Altay C
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Haematologica 2000;85(3):320-1.
2000: Gümrük F; Mergen H; Oner R; Ozcebe O; Sayinalp N; Oner C; Gürgey A; Altay C
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Hemoglobin 2000;24(1):23-9.
2000: Celiker R; Kutsal Y G; Oy B; Onur O; Gürgey A
Depression in children with hemophilic arthropathy and poliomyelitis: a preliminary report.
The Turkish journal of pediatrics 2000;42(1):27-30.
2000: Egesel T; Büyükasik Y; Dündar S V; Gürgey A; Kirazli S; Bayraktar Y
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: Kalayci D; Gürgey A; Güven D; Parlak H; Hasiripi H
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: Koç A; Varan A; Büyükpamukçu M; Gürgey A
A case of hemophilia A associated with Hodgkin's disease.
The Turkish journal of pediatrics 1999;41(4):517-20.
1999: Gürgey A; Yenicesu I; Kanra T; Ozsoylu S; Altay C; Hiçsönmez G; Yetgin S; Tuncer M; Gümrük F; Cetin M
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 cases.
The Turkish journal of pediatrics 1999;41(4):467-71.
1999: Sayinalp N; Ozcebe O I; Kirazli S; Dogan R; Dündar S V; Gürgey A
Paget-Schroetter syndrome associated with FV:Q506 and prothrombin 20210A--a case report.
Angiology 1999;50(8):689-92.
1999: Oner A F; Gürgey A; Okur H; Kirazli S; Gümrük F; Altay C
Changes of hemostatic factors in patients with hemoglobinopathies.
The Turkish journal of pediatrics 1999;41(3):323-7.
1999: Gürakan F; Gürgey A; Bakkaloglu A; Koçak N
Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome.
Journal of pediatric gastroenterology and nutrition 1999;28(5):516-7.
1999: Balta G; Gürgey A
Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
The Turkish journal of pediatrics 1999;41(2):197-9.
1999: Oner A F; Gürgey A; Kirazli S; Okur H; Tunç B
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: Gürgey A; Hicsönmez G; Parlak H; Balta G; Celiker A
Prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis.
American journal of hematology 1998;59(2):179-80.
1998: Olcay L; Besim A; Senocak M E; Göçmen A; Büyükpamukçu M; Kale G; Cetin M; Gürgey A
Hydatid cyst mimicking pulmonary hematoma in a patient with hemophilia A.
The Turkish journal of pediatrics 1998;40(3):425-9.
1998: Yetgin S; Gürgey A; Tuncer A M; Cetin M; Ozbek N; Sayli T; Güler E; Kara A; Olcay L; Duru F; Gümrük F; Atahan L; Tunçbilek E
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: Oner C; Oner R; Balkan H; Gümrük F; Gürgey A
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: Altay C; Oner C; Oner R; Gümrük F; Mergen H; Gürgey A
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: Oner C; Oner R; Birben E; Balkan H; Gümrük F; Gürgey A; Altay C
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.
Hemoglobin 1998;22(2):157-60.
1998: Oner A F; Gürgey A; Gürler A; Mesci L
Factor V Leiden mutation in patients with Behçet's disease.
The Journal of rheumatology 1998;25(3):496-8.
1998: Saçkesen C; Seçmeer G; Gürgey A; Kanra G; Ecevit Z; Ceyhan M; Bulun A; Kara A; Türkmen O; Parlak H
Homozygous Factor V Leiden mutation in a child with meningococcal purpura fulminans.
The Pediatric infectious disease journal 1998;17(1):87.
1998: Gürgey A; Gurler A; Oner A F; Mesci L; Kirazli S
Thrombomodulin levels in Behçet's disease with and without the factor V Leiden mutation.
Clinical rheumatology 1998;17(3):186-8.
1997: Olcay L; Gürgey A; Topaloglu H; Altay S; Parlak H; Firat M
Cerebral infarct associated with factor V Leiden mutation in a boy with hemophilia A.
American journal of hematology 1997;56(3):189-90.
1997: Cetin M; Gürgey A; Gümrük F; Altay C
Serum erythropoietin in children with iron deficiency anemia.
The Turkish journal of pediatrics 1997;39(4):459-64.
1997: Yetgin S; Olcay L; Ozsoylu S; Hiçsönmez G; Gürgey A; Tuncer A M
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: Gürgey A; Büyükpamukcu M; Baskut C; Yalcin B; Gögüs S
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: Gürgey A; Gögüs S; Saatçi U; Bilginturan N; Yordam N; Coskun T; Ozkutlu S; Sahin N
Leprechaunism in two Turkish patients.
The Turkish journal of pediatrics 1997;39(3):387-93.
1997: Gürgey A; Mesci L
The prevalence of factor V Leiden (1691 G-->A) mutation in Turkey.
The Turkish journal of pediatrics 1997;39(3):313-5.
1997: Altay C; Oner C; Oner R; Mesci L; Balkan H; Tüzmen S; Basak A N; Gümrük F; Gürgey A
Genotype-phenotype analysis in HbS-beta-thalassemia.
Human heredity 1997;47(3):161-4.
1997: Gürgey A; Balkan H; Irken G; Gümrük F; Altay S; Kalaycioglu A; Oner C; Oner R
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: Oner C; Oner R; Balkan H; Gürgey A; Yalçin A; Avcu F; Altay C
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
British journal of haematology 1997;96(2):229-34.
1997: Celiker R; Olcay L; Kara A; Gürgey A
Clinical and radiological assessment of haemophilic arthropathy in children.
Clinical rheumatology 1997;16(1):109-10.
1997: Oner C; Gürgey A; Oner R; Balkan H; Gümrük F; Baysal E; Altay C
The molecular basis of Hb H disease in Turkey.
Hemoglobin 1997;21(1):41-51.
1997: Hiçsönmez G; Gümrük F; Zamani P V; Tuncer M A; Yetgin S; Gürgey A; Atahan L; Ozsoylu S
High-dose methylprednisolone for children with acute lymphoblastic leukemia and unfavorable presenting features.
European journal of haematology 1997;58(1):26-31.
1997: Caglayan S H; Gökmen Y; Aktuglu G; Gürgey A; Sommer S S
Mutations associated with hemophilia B in Turkish patients.
Human mutation 1997;10(1):76-9.
1996: Kanra T; Erdem G; Tekinalp G; Gürgey A; Yigit S; Dogru D
Further hemolytic disease of the newborn caused by anti-M.
American journal of hematology 1996;53(4):280-1.
1996: Tekinalp G; Oran O; Gürakan B; Saraçel M; Erdem G; Yurdakök M; Gürgey A
Relationship between maternal and neonatal iron stores.
The Turkish journal of pediatrics 1996;38(4):439-45.
1996: Gürgey A; Ozalp I; Rötig A; Coskun T; Tekinalp G; Erdem G; Akeören Z; Caglar M; Bakkaloglu A
A case of Pearson syndrome associated with multiple renal cysts.
Pediatric nephrology (Berlin, Germany) 1996;10(5):637-8.
1996: Smetanina N S; Oner C; Baysal E; Oner R; Bozkurt G; Altay C; Gürgey A; Adekile A D; Gu L H; Huisman T H
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: Altay C; Gürgey A; Basak A N; Tadmouri G O; Schroeder-Kurt T
Fanconi aplastic anemia associated with beta-thalassemia trait.
American journal of hematology 1996;52(3):239-40.
1996: Olcay L; Ozer S; Gürgey A; Saraçlar M; Ozme S; Bilgiç A; Ozkutlu S; Celiker A
Parameters of iron deficiency in children with cyanotic congenital heart disease.
Pediatric cardiology 1996;17(3):150-4.
1996: Gürgey A; Sayli T; Kara A; Kale G; Berkel I
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: Gürgey A; Beksaç S; Gümrük E; Cakar N; Mesçi L; Altay S; Oner C; Altay C
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience.
Pediatric hematology and oncology 1996;13(2):163-6.
1996: Altay C; Yilgör E; Beksac S; Gürgey A
Premarital screening of hemoglobinopathies: a pilot study in Turkey.
Human heredity 1996;46(2):112-4.
1996: Oner R; Oner C; Erdem G; Balkan H; Ozdag H; Erkan M; Gümrük F; Gürgey A; Altay C
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: Gürgey A; Mesci L; Ozerkam K; Oner C
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: Gürgey A; Altay C; Gu L H; Leonova J Y; Delibalta A; Oner C; Huisman T H
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: Cetin M; Kara A; Gürgey A; Gümrük F; Irken G; Yetgin S; Altay C
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: Oner C; Oner R; Gürgey A; Altay C
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: Hiçsönmez G; Cetin M; Tuneer M A; Gümrük F; Ozbek N; Kara A; Gürgey A
High-dose methylprednisolone for remission induction in hypoplastic acute myeloid leukemia.
European journal of haematology 1995;54(2):125-6.
1995: Gürgey A; Bilginturan N; Yordam N; Vidinlisan S; Altay C; Diskapi S S
Anemia associated with diabetes mellitus.
Pediatric hematology and oncology 1995;12(1):83-5.
1994: Duru F; Gürgey A
Effect of corticosteroids in hereditary spherocytosis.
Acta paediatrica Japonica; Overseas edition 1994;36(6):666-8.
1994: Yalçin A; Avcu F; Beyan C; Gürgey A; Ural A U
A case of HB J-Meerut (or Hb J-Birmingham) [alpha 120(H3)Ala-->Glu]
Hemoglobin 1994;18(6):433-5.
1994: Besbas N; Ozen S; Bakkaloglu A; Gürgey A; Kanra T; Saatçi U
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: Gürgey A; Kalayci O; Gümrük F; Cetin M; Altay C
Convulsion after blood transfusion in four beta-thalassemia intermedia patients.
Pediatric hematology and oncology 1994;11(5):549-52.
1994: Gürgey A; Yüce A; Ozbek N; Koçak N
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: Duru F; Gümrük F; Gürgey A
Vacuolated white blood cells in thalassemia major.
The Turkish journal of pediatrics 1994;36(3):255-8.
1994: Efremov D G; Dimovski A J; Baysal E; Ye Z; Adekile A D; Ribeiro M L; Schiliro G; Altay C; Gürgey A; Efremov G D
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: Gürgey A; Kara A; Tuncer M; Alikasifoglu M; Tunçbilek E
Acute lymphoblastic leukemia associated with Klinefelter syndrome.
Pediatric hematology and oncology 1994;11(2):227-9.
1994: Sayli T R; Basak A N; Gümrük F; Gürgey A; Altay C
Imerslund-Gräsbeck syndrome coexisting with beta-thalassemia trait.
Pediatric hematology and oncology 1994;11(2):223-5.
1994: Dursun A; Kubar A; Gokoz A; Duru F; Gürgey A
Neutral lipid storage disease co-existing with ichthyosiform dermatosis.
European journal of pediatrics 1994;153(3):210-1.
1994: Duru F; Gürgey A; Cetin M; Kanra T; Altay C
Chronic autoimmune hemolytic anemia in children: a report of four patients.
Journal of medicine 1994;25(3-4):231-40.
1994: Cetin M; Yetgin S; Kara A; Tuncer A M; Günay M; Gümrük F; Gürgey A
Hyperglycemia, ketoacidosis and other complications of L-asparaginase in children with acute lymphoblastic leukemia.
Journal of medicine 1994;25(3-4):219-29.
1993: Cürük M A; Dimovski A J; Baysal E; Gu L H; Kutlar F; Molchanova T P; Webber B B; Altay C; Gürgey A; Huisman T H
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: Mesci L; Gürgey A; Altay C
Recent progress in DNA technology.
The Turkish journal of pediatrics 1993;35(3):239-40.
1993: Gürgey A; Beksaç S; Mesci L; Cakar N; Karakas U; Kutlar A; Altay C
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
The Turkish journal of pediatrics 1993;35(3):159-62.
1993: Sayli T; Cemeroglu A P; Tuncer A M; Gürgey A
Acute lymphoblastic leukemia following optic glioma treated by radiotherapy and surgery.
Acta paediatrica (Oslo, Norway : 1992) 1993;82(3):327-8.
1992: Duru F; Gürgey A; Oztürk G; Yörükan S; Altay C
Homozygosity for dominant form of hereditary spherocytosis.
British journal of haematology 1992;82(3):596-600.
1992: Gümrük F; Gürgey A; Duru F; Altay C
Reevaluation of iron absorption and serum ferritin in beta-thalassemia intermedia.
Pediatric hematology and oncology 1992;9(4):359-63.
1992: Basak A N; Ozçelik H; Ozer A; Tolun A; Aksoy M; Agaoglu L; Ridolfi F; Ulukutlu L; Akar N; Gürgey A
The molecular basis of beta-thalassemia in Turkey.
Human genetics 1992;89(3):315-8.
1992: Gürgey A; Rötig A; Gümrük F; Cemeroglu P; Sarialioglu F; Altay C
Pearson's marrow-pancreas syndrome in 2 Turkish children.
Acta haematologica 1992;87(4):206-9.
1992: Basak A N; Ozer A; Ozçelik H; Kirdar B; Gürgey A
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: Gürgey A; Ozsoylu S; Hiçsönmez G; Irken G; Altay C
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran.
The Turkish journal of pediatrics 1990;32(1):39-41.
1990: Altay C; Gürgey A
Beta-thalassemia intermedia in Turkey.
Annals of the New York Academy of Sciences 1990;612():81-9.
1989: Hiçsönmez G; Ozsoylu S; Gürgey A; Zamani V P; Irken G
High-dose methylprednisolone for remission induction in children with acute nonlymphoblastic leukemia.
European journal of haematology 1989;42(5):498-500.
1989: Ozsoylu S; Irken G; Gürgey A
High dose intravenous methylprednisolone for Kassabach-Merritt syndrome.
European journal of pediatrics 1989;148(5):403-5.
1988: Hiçsönmez G; Gürgey A; Zamani V P; Yetgin S; Altay C; Ozsoylu S
Poor prognosis in children with acute nonlymphoblastic leukemia in Turkey.
The American journal of pediatric hematology/oncology 1988;10(3):268-72.
1987: Gürgey A; Hiçsönmez G; Balci S; Ertürk G; Irken G
Leukemias associated with neurofibromatosis in children.
The Turkish journal of pediatrics 1987;29(3):171-6.
1983: Osman S; Gürgey A; Zamani V P; Altay C
Changes in serum elements of childhood acute lymphoblastic leukemia before and during therapy.
The Turkish journal of pediatrics 1983;25(4):233-43.
1983: Gürgey A; Ozsoylu S; Kanra T; Ertürk G
A case of autoimmune hemolytic anemia following thrombocytopenia.
The Turkish journal of pediatrics 1983;25(1):63-7.
1982: Hiçsönmez G; Ozsoylu S; Yetgin S; Zamani V; Gürgey A; Atahan I
Prognosis in 262 Turkish children with acute lymphocytic leukemia.
The Turkish journal of pediatrics 1982;24(3):159-67.

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