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Aytemiz Gurgey

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Co-Publications
Name
28
Altay, Cigdem
18
Gumruk, Fatma
16
Huisman, TH
13
Balta, Gunay
12
Kutlar, Ferdane
10
Kutlar, Abdullah
9
Unal, Sule
8
Cetin, Mualla
7
Aksoy, Cemalettin
7
Tavil, Betul
7
Tekinalp, Gülsevin
5
Ozyurek, Emel
5
Kuskonmaz, Baris
4
Efremov, Georgi
4
Okur, Hamza

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Publications

TOP 3
Oner Ahmet Faik; Okur Hamza; Balta Gunay; Unal Sule; Deger Ibrahim; Akarsu Nurten; Gurgey Aytemiz
Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene.
Tavil Betul; Sanal Ozden; Turul Tuba; Yel Leman; Gurgey Aytemiz; Gumruk Fatma
Parvovirus B19-induced persistent pure red cell aplasia in a child with T-cell immunodeficiency.
Tavil Betul; Kuskonmaz Baris; Kiper Nural; Cetin Mualla; Gumruk Fatma; Gurgey Aytemiz
Pulmonary thromboembolism in childhood: a single-center experience from Turkey.

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All Publications

2009: Oner Ahmet Faik; Okur Hamza; Balta Gunay; Unal Sule; Deger Ibrahim; Akarsu Nurten; Gurgey Aytemiz
Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene.
Leukemia research 2009;33(9):e152-3.
2009: Tavil Betul; Sanal Ozden; Turul Tuba; Yel Leman; Gurgey Aytemiz; Gumruk Fatma
Parvovirus B19-induced persistent pure red cell aplasia in a child with T-cell immunodeficiency.
Pediatric hematology and oncology 2009;26(2):63-8.
2009: Tavil Betul; Kuskonmaz Baris; Kiper Nural; Cetin Mualla; Gumruk Fatma; Gurgey Aytemiz
Pulmonary thromboembolism in childhood: a single-center experience from Turkey.
Heart & lung : the journal of critical care 2009;38(1):56-65.
2008: Gumruk Fatma; Tavil Betul; Balta Gunay; Unal Selma; Gurgey Aytemiz
Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: reevaluation of fetal hemoglobin values by a sensitive method.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2008;30(12):896-9.
2008: Gurgey Aytemiz; Unal Sule; Okur Hamza; Orhan Diclehan; Yurdakok Murat
Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2008;30(12):871-6.
2008: Onalan Orhan; Balta Gunay; Oto Ali; Kabakci Giray; Tokgozoglu Lale; Aytemir Kudret; Altay Cigdem; Gurgey Aytemiz; Nazli Nasih
Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Journal of thrombosis and thrombolysis 2008;26(3):211-7.
2008: Gurgey Aytemiz; Aytac Selin; Balta Gunay; Oguz Kader K; Gumruk Fatma
Central nervous system involvement in Turkish children with primary hemophagocytic lymphohistiocytosis.
Journal of child neurology 2008;23(11):1293-9.
2008: Kuskonmaz Baris; Unal Sule; Cördükcü Emine; Aydin Halil; Coskun Turgay; Gurgey Aytemiz; Gumruk Fatma
Lymphocytic vacuolization in sialic acid storage disease.
American journal of hematology 2008;83(10):821.
2008: Balci Yasemin Isik; Unal Sule; Gumruk Fatma; Cetin Mualla; Ozkutlu Suheyla; Gurgey Aytemiz
Nonstroke arterial thrombosis in children: Hacettepe experience.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(6):519-24.
2008: Okur Hamza; Balta Gunay; Akarsu Nurten; Oner Ahmet; Patiroglu Turkan; Bay Ali; Sayli Tulin; Unal Sule; Gurgey Aytemiz
Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations.
Leukemia research 2008;32(6):972-5.
2008: Gursoy Tugba; Tekinalp Gulsevin; Yigit Sule; Kirazli Serafettin; Korkmaz Ayse; Gurgey Aytemiz
Thrombin activatable fibrinolysis inhibitor activity (TAFIa) levels in neonates with meconium-stained amniotic fluid.
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 2008;21(2):123-8.
2008: Unal Selma; Gumruk Fatma; Aytac Selin; Yalnzoglu Dilek; Gurgey Aytemiz
Interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha) levels and IL-6, TNF-polymorphisms in children with thrombosis.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2008;30(1):26-31.
2008: Gursoy Tugba; Tekinalp Gulsevin; Yurdakok Murat; Ozcebe Osman; Korkmaz Ayse; Gurgey Aytemiz
Thrombin activatable fibrinolysis inhibitor activity, thrombin-antithrombin complex and D-dimer levels in preterm neonates with early respiratory distress syndrome.
American journal of hematology 2008;83(1):50-3.
2007: Tavil Betul; Ozyurek Emel; Gumruk Fatma; Cetin Mualla; Gurgey Aytemiz
Antiphospholipid antibodies in Turkish children with thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2007;18(4):347-52.
2007: Ozgur Tuba Turul; Asal Gulten Turkkan; Gurgey Aytemiz; Tezcan Ilhan; Ersoy Fugen; Sanal Ozden
Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2007;29(5):327-9.
2007: Harmanci Ozgur; Ersoy Osman; Gurgey Aytemiz; Buyukasik Yahya; Gedikoglu Gokhan; Balkanci Ferhun; Sivri Bulent; Bayraktar Yusuf
The etiologic distribution of thrombophilic factors in chronic portal vein thrombosis.
Journal of clinical gastroenterology 2007;41(5):521-7.
2007: Kuijpers Taco W; van Bruggen Robin; Kamerbeek Nanne; Tool Anton T J; Hicsonmez Gonul; Gurgey Aytemiz; Karow Axel; Verhoeven Arthur J; Seeger Karl; Sanal Ozden; Niemeyer Charlotte; Roos Dirk
Natural history and early diagnosis of LAD-1/variant syndrome.
Blood 2007;109(8):3529-37.
2006: Yurekli Banu Pinar Sarer; Aksoy Duygu Yazgan; Aybar Melda; Egesel Turker; Gurgey Aytemiz; Hascelik Gulsen; Kirazli Serafettin; Haznedaroglu Ibrahim Celalettin; Arslan Serap
The search for a common thrombophilic state during the active state of inflammatory bowel disease.
Journal of clinical gastroenterology 2006;40(9):809-13.
2006: Tavil Betul; Sivri Hatice Serapl Kalkanoglu; Coskun Turgay; Gurgey Aytemiz; Ozyurek Emel; Dursun Ali; Tokatli Aysegul; Altay Cigdem; Gumruk Fatma
Haematological findings in children with inborn errors of metabolism.
Journal of inherited metabolic disease 2006;29(5):607-11.
2006: Kuskonmaz Baris; Duzova Ali; Kanbur Nuray Oksuz; Gurakan Figen; Gumruk Fatma; Gurgey Aytemiz
Hemophagocytic syndrome and acute liver failure associated with ethylene glycol ingestion: a case report.
Pediatric hematology and oncology 2006;23(5):427-32.
2006: Ozgen B; Karli-Oguz K; Sarikaya B; Tavil B; Gurgey A
Diffusion-weighted cranial MR imaging findings in a patient with hemophagocytic syndrome.
AJNR. American journal of neuroradiology 2006;27(6):1312-4.
2006: Kuskonmaz Baris; Unal Sule; Gumruk Fatma; Cetin Mualla; Tuncer A Murat; Gurgey Aytemiz
The neurologic complications in pediatric acute lymphoblastic leukemia patients excluding leukemic infiltration.
Leukemia research 2006;30(5):537-41.
2006: Ozyurek Emel; Okur Hamza; Gurgey Aytemiz
Effect of short course high dose methylprednisolone on endothelin-1 and nitric oxide in children with acute lymphoblastic leukemia: a preliminary study.
Annals of hematology 2006;85(1):55-7.
2006: Onderoglu L; Baykal C; Al R A; Demirtas E; Deren O; Gurgey A
High frequency of thrombophilic disorders in women with recurrent fetal miscarriage.
Clinical and experimental obstetrics & gynecology 2006;33(1):50-4.
2005: Gurgey Aytemiz; Secmeer Gulten; Tavil Betul; Ceyhan Mehmet; Kuskonmaz Baris; Cengiz Bulent; Ozen Hasan; Kara Ates; Cetin Mualla; Gumruk Fatma
Secondary hemophagocytic lymphohistiocytosis in Turkish children.
The Pediatric infectious disease journal 2005;24(12):1116-7.
2005: Alikasifoglu Ayfer; Yetgin Sevgi; Cetin Mualla; Tuncer Murat; Gumruk Fatma; Gurgey Aytemiz; Yordam Nursen
Bone mineral density and serum bone turnover markers in survivors of childhood acute lymphoblastic leukemia: comparison of megadose methylprednisolone and conventional-dose prednisolone treatments.
American journal of hematology 2005;80(2):113-8.
2005: Kazanci Ebru; Oguz Kader Karli; Gurgey Aytemiz; Topçu Meral
Streptococcus oralis as a risk factor for middle cerebral artery thrombosis.
Journal of child neurology 2005;20(7):611-3.
2005: Gurgey Aytemiz; Unal Selma; Okur Hamza; Duru Feride; Gumruk Fatma
Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T.
Pediatric hematology and oncology 2005;22(4):309-14.
2005: Cinar Asli; Dilber Embiya; Karagoz Tevfik; Bahadir Nursat; Gucer Safak; Tekinalp Gulsevin; Gurgey Aytemiz
Association of prothrombin gene mutation with sepsis in a preterm with multiple intracardiac thrombi.
Echocardiography (Mount Kisco, N.Y.) 2005;22(4):340-4.
2004: Gurgey Aytemiz; Balta Gunay; Gumruk Fatma; Altay Cigdem
Analysis of some clinical and laboratory aspects of adolescent patients with thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(8):657-62.
2004: Gurgey Aytemiz; Tekinalp Gulsevin; Cinar Asli; Cakmak Fatmanur
Symptomatic thrombosis in Turkish neonates.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2004;26(7):417-20.
2004: Aygun Canan; Tekinalp Gülsevin; Gurgey Aytemiz
Increased fetal iron load in rhesus hemolytic disease.
Pediatric hematology and oncology 2004;21(4):329-33.
2004: Unal Selma; Balta Gunay; Duru Feride; Gumruk Fatma; Altay Cigdem; Gurgey Aytemiz
Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(4):343-6.
2003: Koc A; Gumruk F; Gurgey A
The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: a preliminary study.
Pediatric hematology and oncology 2003;20(6):429-34.
2003: Balta Gunay; Gumruk Fatma; Akarsu Nurten; Gurgey Aytemiz; Altay Cigdem
Molecular characterization of Turkish patients with pyrimidine 5' nucleotidase-I deficiency.
Blood 2003;102(5):1900-3.
2003: Aygun Canan; Tekinalp Gülsevin; Gurgey Aytemiz
Infection-associated hemophagocytic syndrome due to Pseudomonas aeruginosa in preterm infants.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2003;25(8):665-7.
2003: Balta Gunay; Yuksek Nazmiye; Ozyurek Emel; Ertem Ulya; Hicsonmez Gonul; Altay Cigdem; Gurgey Aytemiz
Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia.
American journal of hematology 2003;73(3):154-60.
2003: Gurgey A; Ozyurek E; Gümrük F; Celiker A; Ozkutlu S; Ozer S; Bilgiç A
Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations.
Pediatric cardiology 2003;24(3):244-8.
2003: Balta G; Altay C; Gurgey A
Prevalence of PAI-1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review.
Journal of thrombosis and haemostasis : JTH 2003;1(4):858-9.
2003: Gurgey Aytemiz; Balta Gunay; Boyvat Ayse
Factor V Leiden mutation and PAI-1 gene 4G/5G genotype in thrombotic patients with Behcet's disease.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003;14(2):121-4.
2003: Dogan Yasar; Aygun Denizmen; Yilmaz Yelda; Kanra Guler; Secmeer Gulten; Besbas Nesrin; Gurgey Aytemiz
Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminans.
Pediatric hematology and oncology 2003;20(1):1-5.
2002: Yigit S; Tekinalp G; Oran O; Yurdakok M; Aliefendioglu D; Gurgey A
Endothelin 1 concentrations in infants with meconium stained amniotic fluid.
Archives of disease in childhood. Fetal and neonatal edition 2002;87(3):F212-3.
2002: Balta Gunay; Altay Cigdem; Gurgey Aytemiz
PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs.
American journal of hematology 2002;71(2):89-93.
2001: Gurgey A; Haznedaroglu I C; Egesel T; Buyukasik Y; Ozcebe O I; Sayinalp N; Dundar S V; Bayraktar Y
Two common genetic thrombotic risk factors: factor V Leiden and prothrombin G20210A in adult Turkish patients with thrombosis.
American journal of hematology 2001;67(2):107-11.
2001: Gurgey A; Aslan D
Outcome of noncatheter-related thrombosis in children: influence of underlying or coexisting factors.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2001;23(3):159-64.
2001: Balta G; Gurgey A; Kudayarov D K; Tunc B; Altay C
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan.
Thrombosis research 2001;101(4):231-4.
2000: Gurgey A; Kudayarov D K; Tuncer M; Parlak H; Altay C
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population.
Thrombosis and haemostasis 2000;84(2):356.
2000: Togrul J; Rustamov R; Gurgey A; Altay S; Altay C
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan.
British journal of haematology 2000;108(4):887-8.
1999: Gurgey A
Clinical manifestations in thrombotic children with factor V Leiden mutation.
Pediatric hematology and oncology 1999;16(3):233-7.
1998: Tezcan I; Xu W; Gurgey A; Tuncer M; Cetin M; Oner C; Yetgin S; Ersoy F; Aizencang G; Astrin K H; Desnick R J
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation.
Blood 1998;92(11):4053-8.
1998: Gurgey A; Rustemov R; Parlak H; Balta G
Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan.
Thrombosis and haemostasis 1998;80(3):520-1.
1996: Gurgey A; Mesci L; Renda Y; Olcay L; Kocak N; Erdem G
Factor V Q 506 mutation in children with thrombosis.
American journal of hematology 1996;53(1):37-9.
1996: Ozbek N; Unsal M; Kara A; Gumruk F; Gurgey A
Treatment of hemophilic pseudotumor with low-dose radiotherapy.
The Turkish journal of pediatrics 1996;38(1):91-4.
1996: Kalayci O; Cetin M; Kirel B; Ozdirim E; Yetgin S; Aysun S; Gurgey A
Neurologic findings of vitamin B12 deficiency: presentation of 7 cases.
The Turkish journal of pediatrics 1996;38(1):67-72.
1994: Gurgey A; Sayli T; Gunay M; Ersoy F; Kucukali T; Kale G; Caglar M
High-dose methylprednisolone and VP-16 in treatment of Griscelli syndrome with central nervous system involvement.
American journal of hematology 1994;47(4):331-2.
1994: Ozen S; Damarguc I; Besbas N; Saatci U; Kanra T; Gurgey A
A case of mumps associated with acute hemolytic crisis resulting in hemoglobinuria and acute renal failure.
Journal of medicine 1994;25(3-4):255-9.
1992: Hicsönmez G; Karadeniz N; Zamani V P; Tuncer A M; Gümrük F; Erturk G; Gurgey A; Ozsoylu S
High remission rate in acute myeloblastic leukemia in children treated with high-dose methylprednisolone.
European journal of haematology 1992;48(4):215-20.
1992: Oner C; Dimovski A J; Altay C; Gurgey A; Gu Y C; Huisman T H; Lanclos K D
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes.
Blood 1992;79(3):813-9.
1992: Fei Y J; Oner R; Bözkurt G; Gu L H; Altay C; Gurgey A; Fattoum S; Baysal E; Huisman T H
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
Acta haematologica 1992;88(2-3):82-5.
1991: Gumruk F; Hiçsónmez G; Ozsoylu S; Gurgey A; Tuncer A M
High-dose methylprednisolone for the treatment of priapism in childhood leukemia.
Pediatric hematology and oncology 1991;8(4):367-8.
1991: Kutlar F; Moscoso H; Kiefer C R; Garver F A; Beksaç S; Onderoglu L; Gurgey A; Altay C; Huisman T H
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.
Journal of chromatography 1991;567(2):359-68.
1991: Altay C; Gurgey A; Oner R; Kutlar A; Kutlar F; Huisman T H
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin 1991;15(4):327-30.
1991: Oner R; Agarwal S; Dimovski A J; Efremov G D; Petkov G H; Altay C; Gurgey A; Huisman T H
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
Hemoglobin 1991;15(1-2):67-76.
1990: Oner C; Gurgey A; Altay C; Kutlar F; Huisman T H
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.
American journal of hematology 1990;34(3):230-1.
1990: Gurgey A; Sipahioglu M; Aksoy M
Compound heterozygosity for Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys and beta-thalassemia type IVS-I-6 (T----C)
Hemoglobin 1990;14(4):449-51.
1990: Oner R; Altay C; Gurgey A; Aksoy M; Kilinç Y; Stoming T A; Reese A L; Kutlar A; Kutlar F; Huisman T H
Beta-thalassemia in Turkey.
Hemoglobin 1990;14(1):1-13.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar A; Kutlar F; Lanclos K D; Howard E F; Fei Y J; Aksoy M; Altay C; Gurgey A
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
Blood 1989;73(6):1705-11.
1989: Kutlar F; Gonzalez-Redondo J M; Kutlar A; Gurgey A; Altay C; Efremov G D; Kleman K; Huisman T H
The levels of zeta, gamma, and delta chains in patients with Hb H disease.
Human genetics 1989;82(2):179-86.
1989: Gurgey A; Altay C; Beksaç M S; Bhattacharya R; Kutlar F; Huisman T H
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
Acta haematologica 1989;81(3):169-71.
1989: Kutlar A; Kutlar F; Aksoy M; Gurgey A; Altay C; Wilson J B; Diaz-Chico J C; Hu H; Huisman T H
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
Hemoglobin 1989;13(1):7-16.
1989: Gurgey A; Altay C; Diaz-Chico J C; Kutlar F; Kutlar A; Huisman T H
Molecular heterogeneity of beta-thalassemia intermedia in Turkey.
Acta haematologica 1989;81(1):22-7.
1988: Fei Y J; Stoming T A; Efremov G D; Efremov D G; Battacharia R; Gonzalez-Redondo J M; Altay C; Gurgey A; Huisman T H
Beta-thalassemia due to a T----A mutation within the ATA box.
Biochemical and biophysical research communications 1988;153(2):741-7.
1988: Diaz-Chico J C; Yang K G; Stoming T A; Efremov D G; Kutlar A; Kutlar F; Aksoy M; Altay C; Gurgey A; Kilinc Y
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
Blood 1988;71(1):248-51.
1988: Altay C; Gurgey A; Wilson J B; Hu H; Webber B B; Kutlar F; Huisman T H
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.
Hemoglobin 1988;12(1):87-9.
1986: Yang K G; Liu J Z; Kutlar F; Kutlar A; Altay C; Gurgey A; Huisman T H
Beta zero-thalassemia in association with a gamma-globin gene quadruplication.
Blood 1986;68(6):1394-7.
1986: Aksoy M; Gurgey A; Altay C; Kilinc Y; Carstairs K C; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Some notes about Hb Q-India and Hb Q-Iran.
Hemoglobin 1986;10(2):215-9.
1985: Kilinç Y; Kumi M; Gurgey A; Altay C; Webber B B; Wilson J B; Kutlar A; Huisman T H
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
Hemoglobin 1985;9(6):621-5.
1983: Hicsönmez G; Ozsoylu S; Yetgin S; Zamani V; Gurgey A
Poor prognosis of childhood acute lymphoblastic leukaemia.
British medical journal (Clinical research ed.) 1983;286(6375):1437.
1982: Efremov G D; Ibarra B; Gurgey A; Sukumaran P K; Altay C; Huisman T H
Gamma-chain heterogeneity of fetal hemoglobin in nonblack beta- and delta beta- thalassemia and HPFH heterozygotes and homozygotes.
American journal of hematology 1982;12(4):367-82.
1981: Dincol G; Altay C; Aksoy M; Gurgey A; Felice A E; Huisman T H
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotes.
Hemoglobin 1981;5(2):153-64.

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