Prof. Dr. AYTEMİZ GÜRGEY

Yayın Ağı

Makaleler 84

1. Cohort Study: Central Venous Catheter-Related Complications in Children with Hematologic Diseases at a Single Center

PEKTAŞ A., KARA A., GÜRGEY A.

TURKISH JOURNAL OF HEMATOLOGY , cilt.32, sa.2, ss.144-151, 2015 (SCI-Expanded, Scopus, TRDizin)

2. THE OUTCOME OF PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA IN PATIENTS WHO PRESENTED WITH HYPERLEUKOCYTOSIS

ÜNAL S., ÖZSÜREKCİ Y., AYTAÇ S. A., KUŞKONMAZ B. B., Tavil B., TUNCER M., et al.

PEDIATRIC BLOOD & CANCER , cilt.61, 2014 (SCI-Expanded, Scopus)

3. IMPROVED OUTCOME IN HIGH RISK GROUP PATIENTS WITH HIGH DOSE METHYLPREDNISOLONE DURING INDUCTION OF MODIFIED ST JUDE TOTAL XIIIA

ÜNAL S., Gurgey A., Yetgin S., GÜMRÜK F., TUNCER M., AYTAÇ S. A., et al.

PEDIATRIC BLOOD & CANCER , cilt.60, ss.70, 2013 (SCI-Expanded, Scopus)

4. In vitro characterisation of two ADAMTS13 mutants (I143T, Y570C) identified in two patients with congenital thrombotic thrombocytopenic purpura (TTP)

Underwood M., Garagiola I., Mackie I. J., Machin S. J., Metin A., Gurgey A., et al.

JOURNAL OF THROMBOSIS AND HAEMOSTASIS , cilt.11, ss.491, 2013 (SCI-Expanded, Scopus)

5. Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients

An O., Gursoy A., GÜRGEY A., Keskin O.

PROTEIN SCIENCE , cilt.22, sa.6, ss.823-839, 2013 (SCI-Expanded, Scopus)

6. RECURRENT PEDIATRIC THROMBOSIS: INFLUENCE AND UNDERLYING OR COEXISTING FACTORS

Gokce M., Altan I., ÜNAL S., KUŞKONMAZ B. B., AYTAÇ S. A., ÇETİN M., et al.

HAEMATOLOGICA , cilt.97, ss.192, 2012 (SCI-Expanded, Scopus)

7. Plasminogen Activator Inhibitor 1 4G/5G Polymorphism in Neonatal Respiratory Distress Syndrome

Armangil D., YURDAKÖK M., OKUR H., Gurgey A.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.17, sa.4, ss.352-357, 2011 (SCI-Expanded, Scopus)

8. Prenatal Diagnosis of Hemoglobinopathies in Hacettepe University, Turkey

BEKSAÇ M. S., GÜMRÜK F., Gurgey A., Cakar N., MÜMÜŞOĞLU S., ÖZYÜNCÜ Ö., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.28, sa.1, ss.51-55, 2011 (SCI-Expanded, Scopus)

9. Measles, mumps, and rubella antibody status and response to immunization in children after therapy for acute lymphoblastic leukemia

Aytac Ş. S., YALÇIN Ş., Cetin M., Yetgin S., GÜMRÜK F., Tuncer M., et al.

Pediatric Hematology and Oncology , cilt.27, sa.5, ss.333-343, 2010 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

10. Infectious mononucleosis in Turkish children

Cengiz A. B., Cultu-Kantaroglu O., Secmeer G., Ceyhani M., KARA A., GÜRGEY A.

TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.3, ss.245-254, 2010 (SCI-Expanded, Scopus)

11. Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon

Aytac S., ÜNAL S., Coskun T., Tokatli A., Sivri S., DURSUN A., et al.

HAEMOPHILIA , cilt.16, sa.2, ss.408, 2010 (SCI-Expanded, Scopus)

12. Glanzmann thrombasthenia: Hacettepe experience

Aytac S., ÜNAL S., Cetin M., Gurgey A., Gumruk F.

HAEMOPHILIA , cilt.16, sa.2, ss.408, 2010 (SCI-Expanded, Scopus)

13. Macrothrombocytopenia excluding Bernard Soulier: ten year experience from a single pediatric center

ÜNAL S., Aytac S., Gurgey A., Cetin M., Gumruk F.

HAEMOPHILIA , cilt.16, sa.2, ss.412, 2010 (SCI-Expanded, Scopus)

14. Hydrops fetalis associated with chorioangioma and thrombosis of umbilical vein

Sivasli E., TEKŞAM Ö., HALİLOĞLU M., Gucer S., ORHAN D., GÜRGEY A., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.5, ss.515-518, 2009 (SCI-Expanded, Scopus)

15. Purpura fulminans as the presenting manifestation in a patient with juvenile SLE.

DEMIRKAYA E., CAKMAKLI H., GÜÇER S., AKTAY-AYAZ N., GÜRGEY A., Ozen S.

The Turkish journal of pediatrics , cilt.51, ss.378-80, 2009 (SCI-Expanded, Scopus)

16. 35(th) NATIONAL HEMATOLOGY CONGRESS INTERNATIONAL SESSIONS 10 October 2009 Gloria Golf Resort Hotel Congress Center Antalya, Turkey

Gurgey A.

TURKISH JOURNAL OF HEMATOLOGY , cilt.26, sa.2, ss.46, 2009 (SCI-Expanded, Scopus, TRDizin)

17. Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: a probable new familial syndrome with multisystem involvement

DURSUN A., ÖZGÜL R. K., SOYDAŞ A., Tugrul T., GÜRGEY A., ÇELİKER A., et al.

CLINICAL DYSMORPHOLOGY , cilt.18, sa.1, ss.19-23, 2009 (SCI-Expanded, Scopus)

18. Pulmonary thromboembolism in childhood: A single-center experience from Turkey

Tavil B., Kuskonmaz B. B., Kiper N., Cetin M., Gumruk F., Gurgey A.

HEART & LUNG , cilt.38, sa.1, ss.56-65, 2009 (SCI-Expanded, Scopus)

19. PARVOVIRUS B19-INDUCED PERSISTENT PURE RED CELL APLASIA IN A CHILD WITH T-CELL IMMUNODEFICIENCY

Tavil B., Sanal O., Turul T., Yel L., Gurgey A., Gumruk F.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.26, sa.2, ss.63-68, 2009 (SCI-Expanded, Scopus)

20. Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis

Horne A., Ramme K. G., Rudd E., Zheng C., Wali Y., al-Lamki Z., et al.

BRITISH JOURNAL OF HAEMATOLOGY , cilt.143, sa.1, ss.75-83, 2008 (SCI-Expanded, Scopus)

21. JAK2V617F mutation in patients with portal vein thrombosis

BAYRAKTAR Y., HARMANCI Ö., BÜYÜKAŞIK Y., Shorbagi A. I., Sungur A. H., Boylu C. A., et al.

DIGESTIVE DISEASES AND SCIENCES , cilt.53, sa.10, ss.2778-2783, 2008 (SCI-Expanded, Scopus)

22. Macrothrombocytopenias excluding bernard-soulier syndrome

ÜNAL S., Gurgey A.

HAEMOPHILIA , cilt.14, ss.98, 2008 (SCI-Expanded, Scopus)

23. Influences of factor VIII inhibitor positivity on outcome and chronic arthropathy in hemophilia-A children

ÜNAL S., Aytac S., Gumruk F., Cetin M., Tuncer M., Gurgey A.

HAEMOPHILIA , cilt.14, ss.57, 2008 (SCI-Expanded, Scopus)

24. Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis

Rudd E., Bryceson Y. T., Zheng C., Edner J., Wood S. M., Ramme K., et al.

JOURNAL OF MEDICAL GENETICS , cilt.45, sa.3, ss.134-141, 2008 (SCI-Expanded, Scopus)

25. Thrombin activatable fibrinolysis inhibitor activity, thrombin-antithrombin complex and D-dimer levels in preterm neonates with early respiratory distress syndrome

Gursoy T., Tekinalp G., YURDAKÖK M., Ozcebe O., Korkmaz A., Gurgey A.

AMERICAN JOURNAL OF HEMATOLOGY , cilt.83, sa.1, ss.50-53, 2008 (SCI-Expanded, Scopus)

26. Thrombin activatable fibrinolysis inhibitor activity (TAFIa) levels in neonates with meconium-stained amniotic fluid

Gursoy T., TEKİNALP G., YİĞİT Ş., Kirazli S., KORKMAZ TOYGAR A., GÜRGEY A.

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE , cilt.21, sa.2, ss.123-128, 2008 (SCI-Expanded, Scopus)

27. Interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) levels and IL-6, TNF-polymorphisms in children with thrombosis

Una S., GÜMRÜK F., Aytac Ş. S., YALNIZOĞLU D., GÜRGEY A.

Journal of Pediatric Hematology/Oncology , cilt.30, sa.1, ss.26-31, 2008 (SCI-Expanded, Scopus)

28. Severe proximal renal tubular acidosis in Pearson syndrome

Demirkaya E., Topaloglu R., Rotig A., Coskun T., Topaloglu H., Bakkaloglu A., et al.

PEDIATRIC NEPHROLOGY , cilt.22, sa.9, ss.1633, 2007 (SCI-Expanded, Scopus)

29. Characterization of genotype-phenotype correlations in hemophagocytic lymphohistiocytosis

Horne A., Rudd E., Ericson K. G., Zheng C., Wali Y., al-Lamki Z., et al.

PEDIATRIC BLOOD & CANCER , cilt.48, sa.7, ss.750-751, 2007 (SCI-Expanded, Scopus)

30. Spectrum of MUNC 13-4 gene mutations in familial hemophagocytic lymphohistiocytosis

Rudd E., Zheng C., Edner J., Gurgey A., Wali Y., Hellebostad M., et al.

PEDIATRIC BLOOD & CANCER , cilt.48, sa.7, ss.752, 2007 (SCI-Expanded, Scopus)

31. Anti phospholipid antibodies in Turkish children with thrombosis

Tavil B., Ozyurek E., Gumruk F., Cetin M., Gurgey A.

BLOOD COAGULATION & FIBRINOLYSIS , cilt.18, sa.4, ss.347-352, 2007 (SCI-Expanded, Scopus)

32. The etiologic distribution of thrombophilic factors in chronic portal vein thrombosis

Harmanci O., Ersoy O., Gurgey A., Buyukasik Y., Gedikoglu G., Balkanci F., et al.

JOURNAL OF CLINICAL GASTROENTEROLOGY , cilt.41, sa.5, ss.521-527, 2007 (SCI-Expanded, Scopus)

33. Acquired Factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome

Ozgur T. T., Asal G. T., Gurgey A., Tezcan I., Ersoy F., Sanal O.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.29, sa.5, ss.327-329, 2007 (SCI-Expanded, Scopus)

34. Natural history and early diagnosis of LAD-1/variant syndrome

Kuijpers T. W., van Bruggen R., Kamerbeek N., Tool A. T. J., Hicsonmez G., Gurgey A., et al.

BLOOD , cilt.109, sa.8, ss.3529-3537, 2007 (SCI-Expanded, Scopus)

35. Hypertriglyceridemia and Decreased High-density Lipoprotein Could be a Clue for Visceral Leishmaniasis

Secmeer G., Cengiz A. B., GÜRGEY A., KARA A., Cultu O., Tavil B., et al.

INFECTIOUS DISEASES IN CLINICAL PRACTICE , cilt.14, sa.6, ss.401-402, 2006 (ESCI, Scopus)

36. Prothrombotic risk factors in patients with recurrent thrombosis of the arteriovenous fistula

Tavil B., Bakkaloglu A., Gurgey A.

DIALYSIS & TRANSPLANTATION , cilt.35, sa.11, ss.715-718, 2006 (SCI-Expanded, Scopus)

37. The search for a common thrombophilic state during the active state of inflammatory bowel disease

Yurekli B. P. S., Aksoy D. Y., Aybar M., Egesel T., Gurgey A., Hascelik G., et al.

JOURNAL OF CLINICAL GASTROENTEROLOGY , cilt.40, sa.9, ss.809-813, 2006 (SCI-Expanded, Scopus)

38. Haematological findings in children with inborn errors of metabolism

Tavil B., Sivri H. S. K., Coskun T., Gurgey A., Ozyurek E., DURSUN A., et al.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.29, sa.5, ss.607-611, 2006 (SCI-Expanded, Scopus)

39. Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N

Berber E., Fidanci I. D., Un C., El-Maarri O., Aktuglu G., Gurgey A., et al.

HAEMOPHILIA , cilt.12, sa.4, ss.398-400, 2006 (SCI-Expanded, Scopus)

40. Effect of short course high dose methylprednisolone on endothelin-1 and nitric oxide in children with acute lymphoblastic leukemia: a preliminary study

Ozyurek E., Okur H., Gurgey A.

ANNALS OF HEMATOLOGY , cilt.85, sa.1, ss.55-57, 2006 (SCI-Expanded, Scopus)

41. Bone mineral density and serum bone turnover markers in survivors of childhood acute lymphoblastic leukemia: Comparison of megadose methylprednisolone and conventional-dose prednisolone treatments

Alikasifoglu A., Yetgin S., Cetin M., Tuncer M., Gumruk F., Gurgey A., et al.

AMERICAN JOURNAL OF HEMATOLOGY , cilt.80, sa.2, ss.113-118, 2005 (SCI-Expanded, Scopus)

42. Outcome in children with purpura fulminans: Report on 16 patients

Gurgey A., Aytac Ş. S., Kanra G., Secmeer G., Ceyhan M., Altay C.

American Journal of Hematology , cilt.80, sa.1, ss.20-25, 2005 (SCI-Expanded, Scopus)

43. Streptococcus oralis as a risk factor for middle cerebral artery thrombosis

Kazanci E., Oguz K., Gurgey A., Topcu M.

JOURNAL OF CHILD NEUROLOGY , cilt.20, sa.7, ss.611-613, 2005 (SCI-Expanded, Scopus)

44. Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T

Gurgey A., ÜNAL S., Okur H., Duru F., Gumruk F.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.22, sa.4, ss.309-314, 2005 (SCI-Expanded, Scopus)

45. Evaluation of thrombotic children with malignancy

ÜNAL S., Varan A., Yalcin B., Buyukpamukcu M., Gurgey A.

ANNALS OF HEMATOLOGY , cilt.84, sa.6, ss.395-399, 2005 (SCI-Expanded, Scopus)

46. Association of prothrombin gene mutation with sepsis in a preterm with multiple intracardiac thrombi

Cinar A., Dilber E., Karagoz T., Bahadir N., Gucer S., Tekinalp G., et al.

ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES , cilt.22, sa.4, ss.340-344, 2005 (SCI-Expanded, Scopus)

47. Analysis of pediatric thrombotic patients in Turkey

Oren H., Devecioglu O., Errem M., Vergin C., Kavakli K., Meral A., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.21, sa.7, ss.573-583, 2004 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

48. Symptomatic thrombosis in Turkish neonates

Gurgey A., Tekinalp G., Cinar A., Cakmak F.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.26, sa.7, ss.417-420, 2004 (SCI-Expanded, Scopus)

49. The predictability of factor V Leiden (FV : Q(506)) gene mutation via clotting-based diagnosis of activated protein C resistance

Sayinalp N., Haznedaroglu I., Aksu S., Buyukasik Y., Goker H., Parlak H., et al.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.10, sa.3, ss.265-270, 2004 (SCI-Expanded, Scopus)

50. Increased fetal iron load in rhesus hemolytic disease

Aygun C., Tekinalp G., Gurgey A.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.21, sa.4, ss.329-333, 2004 (SCI-Expanded, Scopus)

51. The effect of short course high dose methylprednisolon therapy on fibrinogen level in children with acute lymphoblastic leukemia - A preliminary study

Tokosz H., ÜNAL S., Kirazli S., Gurgey A.

LEUKEMIA RESEARCH , cilt.28, sa.5, ss.533-535, 2004 (SCI-Expanded, Scopus)

52. Fatal cytophagic histiocytic panniculitis

Secmeer G., Sakalli H., Gok F., Ozen S., Kara A., Cengiz A., et al.

PEDIATRIC DERMATOLOGY , cilt.21, sa.3, ss.246-249, 2004 (SCI-Expanded, Scopus)

53. Acute lymphoblastic leukemia in infants

Gurgey A., Yetgin S., Cetin M., Gumruk F., Tuncer A., Tuncbilek E., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.46, sa.2, ss.115-119, 2004 (SCI-Expanded, Scopus)

54. Molecular characterization of Turkish patients with pyrimidine 5 ' nucleotidase-I deficiency

Balta G., GUMRUK F., AKARSU N., GURGEY A., ALTAY C.

BLOOD , cilt.102, sa.5, ss.1900-1903, 2003 (SCI-Expanded, Scopus)

55. The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: A preliminary study

Koc A., Gumruk F., Gurgey A.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.20, sa.6, ss.429-434, 2003 (SCI-Expanded, Scopus)

56. Use of recombinant factor VIIa for bleeding in children with Glanzmann thrombasthenia.

Caglar K., Cetinkaya A., Aytac Ş. S., Gumruk F., Gurgey A.

Pediatric hematology and oncology , cilt.20, sa.6, ss.435-8, 2003 (SCI-Expanded, Scopus)

57. Infection-associated hemophagocytic syndrome due to Pseudomonas aeruginosa in preterm infants

Aygun C., Tekinalp G., Gurgey A.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.25, sa.8, ss.665-667, 2003 (SCI-Expanded, Scopus)

58. Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients

Birben E., ÖNER C., ÖNER R., ALTAY Ç., Gurgey A.

EUROPEAN JOURNAL OF HAEMATOLOGY , cilt.71, sa.1, ss.39-43, 2003 (SCI-Expanded, Scopus)

59. Primary hemophagocytic lymphohistiocytosis in Turkish children

Gurgey A., Gogus S., Ozyurek E., Aslan D., Gumruk F., Cetin M., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.20, sa.5, ss.367-371, 2003 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

60. Stroke owing to noncompaction of myocardium

Hascelik S., Yalnizoglu D., Kafali G., Celiker A., Cila A., Topcu M., et al.

JOURNAL OF CHILD NEUROLOGY , cilt.18, sa.6, ss.437-439, 2003 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

61. Thrombosis in children with cardiac pathology: Frequency of factor V Leiden and prothrombin G20210A mutations

Gurgey A., Ozyurek E., Gumruk F., Celiker A., Ozkutlu S., Ozer S., et al.

PEDIATRIC CARDIOLOGY , cilt.24, sa.3, ss.244-248, 2003 (SCI-Expanded, Scopus)

62. Prevalence of PAI-1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review

Balta G., ALTAY C., GURGEY A.

JOURNAL OF THROMBOSIS AND HAEMOSTASIS , cilt.1, sa.4, ss.858-859, 2003 (SCI-Expanded, Scopus)

63. Trauma as a risk factor for thrombosis in children: A report of three cases

Ozyurek E., Besbas N., Aslan D., Gurgey A.

TURKISH JOURNAL OF PEDIATRICS , cilt.45, sa.2, ss.167-169, 2003 (SCI-Expanded, Scopus)

64. 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

Yetgin S., Tuncer M., Cetin M., Gumruk F., Yenicesu I., Tunc B., et al.

LEUKEMIA , cilt.17, sa.2, ss.328-333, 2003 (SCI-Expanded, Scopus)

65. Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations

Onay U., Kavakli K., Kilinc Y., Gurgey A., Aktuglu G., Kemahli S., et al.

BRITISH JOURNAL OF HAEMATOLOGY , cilt.120, sa.4, ss.656-659, 2003 (SCI-Expanded, Scopus)

66. The potential effect of short-course high-dose steroid on the maturation and apoptosis of leukemic cells in a child with acute megakaryoblastic leukemia

Hicsonmez G., Cetin M., Okur H., Erdemli E., Gurgey A.

LEUKEMIA & LYMPHOMA , cilt.44, sa.6, ss.1037-1042, 2003 (SCI-Expanded, Scopus)

67. Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis

Ericson K., Fadeel B., Andersson M., Gudmundsson G., Gurgey A., Yalman N., et al.

HUMAN GENETICS , cilt.112, sa.1, ss.98-99, 2003 (SCI-Expanded, Scopus)

68. Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminans

Dogan Y., Aygun D., Yilmaz Y., Kanra G., Secmeer G., Besbas N., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.20, sa.1, ss.1-5, 2003 (SCI-Expanded, Scopus)

69. Griscelli disease: Genotype-phenotype correlation in an array of clinical heterogeneity

Sanal O., Ersoy F., Tezcan I., Metin A., Yel L., Menasche G., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.22, sa.4, ss.237-243, 2002 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

70. Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion

Birben E., ÖNER R., ÖNER C., Gumruk F., ALTAY Ç., Gurgey A.

BRITISH JOURNAL OF HAEMATOLOGY , cilt.118, sa.1, ss.278-281, 2002 (SCI-Expanded, Scopus)

71. Thrombocytopenia and emperipolesis in a patient with hepatitis A infection

Avci Z., Turul T., Catal F., Olgar E., BAYKAN A., Teksam O., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.19, sa.1, ss.67-70, 2002 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

72. Importance of RDW value in differential diagnosis of hypochrome anemias

Aslan D., Gumruk F., Gurgey A., Altay C.

AMERICAN JOURNAL OF HEMATOLOGY , cilt.69, sa.1, ss.31-33, 2002 (SCI-Expanded, Scopus)

73. Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara) 1159 C -> T (387 Arg -> Cys) deficiency associated with Gilbert syndrome in a Turkish patient

Oner R., Acar C., Oner C., Yenicesu I., Gumruk F., Gurgey A., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.19, sa.1, ss.39-44, 2002 (SCI-Expanded, Scopus)

74. Homozygosity for Hb E-Saskatoon [β22(B4)Glu → Lys] in a Turkish patient

BİRBEN E., Ner R., Ner C., GÜMRÜK F., GÜRGEY A., Altay I.

Hemoglobin , cilt.25, sa.4, ss.409-415, 2001 (SCI-Expanded, Scopus)

75. βB-Thalassaemia intermedia in a Turkish girl: Homozygosity for G→A substitution at +22 relative to the β-globin cap site

Öner R., Öner C., BİRBEN E., Sözen M., GÜMRÜK F., GÜRGEY A., et al.

British Journal of Haematology , cilt.115, sa.1, ss.90-94, 2001 (SCI-Expanded, Scopus)

76. Factor V Leiden mutation in Turkish patients with homozygous cystathionine β-synthase deficiency

Kalkanolu H., Cokun T., Aydodu S., TOKATLI A., GÜRGEY A.

Journal of Inherited Metabolic Disease , cilt.24, sa.3, ss.367-369, 2001 (SCI-Expanded, Scopus)

77. Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan

Gurgey A.

THROMBOSIS AND HAEMOSTASIS , cilt.80, sa.3, ss.520-521, 1998 (SCI-Expanded, Scopus)

78. A case of hypereosinophilic syndrome associated with factor V Leiden mutation and thrombosis [1]

GÜMRÜK F., GÜRGEY A., Altay Ç.

British Journal of Haematology , cilt.101, sa.1, ss.208-209, 1998 (SCI-Expanded, Scopus)

79. Homozygous Factor V Leiden mutation in a child with meningococcal purpura fulminans

SACKESEN C., SECMEER G., GURGEY A., KANRA G., CEYHAN M., BULUN A., et al.

PEDIATRIC INFECTIOUS DISEASE JOURNAL , cilt.17, sa.1, ss.87, 1998 (SCI-Expanded, Scopus)

80. Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience

GÜRGEY A., Beksaç S., GÜMRÜK F., Çakar N., Mesçi L., Altay S., et al.

Pediatric Hematology and Oncology , cilt.13, sa.2, ss.163-166, 1996 (Scopus)

81. A Novel (Δβ)°-Thalassemia due to a ∼30-kb Deletion Observed in a Turkish Family

öner R., öner C., ERDEM G., Balkan H., ÖZDAĞ SEVGİLİ H., Erkan M., et al.

Acta Haematologica , cilt.96, sa.4, ss.232-236, 1996 (Scopus)

82. Congenital hypoplastic anemia in six patients: Unusual association of short proximal phalanges with mild anemia

ÇETİN M., Kara A., GÜRGEY A., GÜMRÜK F., Irken G., YETGİN S., et al.

Pediatric Hematology and Oncology , cilt.12, sa.2, ss.153-158, 1995 (Scopus)

83. Convulsion after blood transfusion in four p-thalassemia intermedia patients

GÜRGEY A., Kalaya Ó., Giimriik F., ÇETİN M., Altay C.

Pediatric Hematology and Oncology , cilt.11, sa.5, ss.549-552, 1994 (Scopus)

84. BETA-THALASSEMIA DUE TO A T-]A MUTATION WITHIN THE ATA BOX

FEI Y., STOMING T., EFREMOV G., EFREMOV D., BATTACHARIA R., GONZALEZREDONDO J., et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS , sa.2, ss.741-747, 1988 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 12

1. Clinical and Laboratory Evaluation of Patients with Familial Hemophagocytic Lymphohistiocytosis in a Single Center; Striking the Importance of Central Nervous System and Hepatic Involvement

Beken B., Aytac Ş. S., KUŞKONMAZ B. B., BALTA G., Cetin M., Gurgey A., et al.

56th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2014, cilt.124, (Özet Bildiri)

2. Familial Hemophagocytic Lymphohistiocytosis Type IV: Possible Founder Effect in Syntaxin 11 Gene Common Mutation Endemic to Turkish Population

Caliskan U., Guler E., Patiroglu T., Oner A. F., GÜRGEY A.

50th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2008, cilt.112, ss.456, (Özet Bildiri)

3. Genotyp-Phenotype Correlation in Congenital ADAMTS13 Deficient Patients

Lotta L. A., Garagiola I., Cairo A., Klaassen R., Metin A., GÜRGEY A., et al.

50th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2008, cilt.112, ss.107-108, (Özet Bildiri)

4. HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ASSOCIATED WITH HEMATOLOGIC MALIGNANCIES IN PEDIATRIC AGE GROUP IS AN INDICATIVE OF POOR PROGNOSIS

ÜNAL S., Cetin M., Gumruk E., Gurgey A.

13th Congress of the European-Hematology-Association, Copenhagen, Danimarka, 12 - 15 Haziran 2008, cilt.93, ss.479, (Özet Bildiri)

5. Molecular characterization of a prototype family harboring two genomic instability disorders: Ataxia telangiectasia and fanconi anemia

BALTA G., PATIROĞLU T., GÜMRÜK F., Sanal O., GÜRGEY A., Altay C.

49th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 8 - 11 Aralık 2007, cilt.110, (Özet Bildiri)

6. Natural killer cell count and activity, perforin expression, fas and soluble FAS ligand levels in immunocompetent children with varicella zoster virus infection

ÜNAL S., Bahadir N., Secmeer G., Kara A., Gurgey A.

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.456-457, (Özet Bildiri)

7. Interleukin-6 (IL-6), tumor necrosis factor a (TNF-alpha) levels and IL-6, TNF-polymorphisms in children with thrombosis

ÜNAL S., Aytac S., Gumruk F., Yalnizoglu D., Gurgey A.

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.375, (Özet Bildiri)

8. Pyrimidine 5' nucleotidase-1 (P5N-1) deficiency associated with 4 novel mutations in 5 new Turkish families: Genotype-phenotype analysis.

Balta G., Gurgey A., Gumruk F., Buyukasik Y., Beksac M., Altay C.

48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108, (Özet Bildiri)

9. The retrospective analysis of pediatric acute leukemia cases between 1980-2003: Hacettepe experience.

ÜNAL S., Hicsonmez G., Yetgin S., Gurgey A., Gumruk F., Cetin M., et al.

47th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 10 - 13 Aralık 2005, cilt.106, (Özet Bildiri)

10. Molecular characterization of pyrimidine 5 prime nucleotidase (P5N-1) deficiency: Identification of 3 novel mutations.

Balta G., Gurgey A., Gumruk F., Akarsu N., Altay C.

44th Annual Meeting of the American-Society-of-Hematology, PHILADELPHIA, PENNSYLVANIA, 6 - 10 Aralık 2002, cilt.100, (Özet Bildiri)

11. GSTM1 null, GSTT1 null, GSTP1 (lle105Val) and CYPA1 (T6235C) genotypes in childhood acute leukemia

Balta G., Ozyurek E., Ertem U., Hicsonmez G., Altay C., Gurgey A.

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.89-90, (Özet Bildiri)

12. Association of PAI-1 gene 4G/5G genotype with Coronary Artery Disease

Balta G., Onalan O., Oto A., Gurgey A., Altay C.

Metrikler

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

915

H-İndeks (WoS)

Atıf (Scopus)

595

H-İndeks (Scopus)

Proje

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler