Metrikler
Yayın
96
Açık Erişim
2
BM Sürdürülebilir Kalkınma Amaçları
Makaleler
Tümü (84)
SCI-E, SSCI, AHCI (79)
SCI-E, SSCI, AHCI, ESCI (80)
ESCI (1)
Scopus (84)
TRDizin (2)
2015
20151. 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)
2014
20142. 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)
2013
20133. 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)
2013
20134. 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)
2013
20135. 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)
2012
20126. 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)
2011
20117. 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)
2011
20118. 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)
2010
20109. 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)
2010
201010. 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)
2010
201011. 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)
2010
201012. 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)
2010
201013. 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)
2009
200914. 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)
2009
200915. 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)
2009
200916. 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)
2009
200917. 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)
2009
200918. 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)
2009
200919. 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)
2008
200820. 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)
2008
200821. 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)
2008
200822. Macrothrombocytopenias excluding bernard-soulier syndrome
ÜNAL S., Gurgey A.
HAEMOPHILIA
, cilt.14, ss.98, 2008 (SCI-Expanded, Scopus)
2008
200823. 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)
2008
200824. 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)
2008
200825. 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)
2008
200826. 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)
2008
200827. 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)
2007
200728. 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)
2007
200729. 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)
2007
200730. 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)
2007
200731. 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)
2007
200732. 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)
2007
200733. 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)
2007
200734. 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)
2006
200635. 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)
2006
200636. 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)
2006
200637. 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)
2006
200638. 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)
2006
200639. 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)
2006
200640. 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)
2005
200541. 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)
2005
200542. 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)
2005
200543. 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)
2005
200544. 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)
2005
200545. 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)
2005
200546. 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)
2004
200447. 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)
2004
200448. 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)
2004
200449. 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)
2004
200450. 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)
2004
200451. 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)
2004
200452. 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)
2004
200453. 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)
2003
200354. 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)
2003
200355. 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)
2003
200356. 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)
2003
200357. 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)
2003
200358. 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)
2003
200359. 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)
2003
200360. 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)
2003
200361. 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)
2003
200362. 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)
2003
200363. 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)
2003
200364. 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)
2003
200365. 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)
2003
200366. 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)
2003
200367. 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)
2003
200368. 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)
2002
200269. 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)
2002
200270. 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)
2002
200271. 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)
2002
200272. 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)
2002
200273. 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)
2001
200174. 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)
2001
200175. 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)
2001
200176. 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)
1998
199877. 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)
1998
199878. 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)
1998
199879. 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)
1996
199680. 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)
1996
199681. 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)
1995
199582. 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)
1994
199483. 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)
1988
198884. 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)
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2008
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13th Congress of the European-Hematology-Association, Copenhagen, Danimarka, 12 - 15 Haziran 2008, cilt.93, ss.479, (Özet Bildiri)
2007
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49th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 8 - 11 Aralık 2007, cilt.110, (Özet Bildiri)
2007
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12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.456-457, (Özet Bildiri)
2007
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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)
2006
20068. Pyrimidine 5' nucleotidase-1 (P5N-1) deficiency associated with 4 novel mutations in 5 new Turkish families: Genotype-phenotype analysis.
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48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108, (Özet Bildiri)
2005
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2002
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2002
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2002
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