Publications by authors named "Gunay Balta"

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Fanconi Anemia and Ataxia Telangiectasia in Siblings who Inherited Unique Combinations of Novel FANCA and ATM Null Mutations.
Gunay Balta, Turkan Patiroglu, Fatma Gumruk

J Pediatr Hematol Oncol· April 2019

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Bone marrow mesenchymal stem cell donors with a high body mass index display elevated endoplasmic reticulum stress and are functionally impaired.
Baris Ulum, Hikmet Taner Teker, Aysun Sarikaya, Gunay Balta, Baris Kuskonmaz

J Cell Physiol· November 2018

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The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience.
Burcin Beken, Selin Aytac, Gunay Balta, Baris Kuskonmaz, Duygu Uckan

Haematologica· February 2018

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Survey of Hfe Gene C282Y Mutation in Turkish Beta-Thalassemia Patients and Healthy Population: A Preliminary Study.
Selma Unal, Günay Balta, Fatma Gümrük, Hong-Gui Xu

Turk J Haematol· September 2014

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Defective UNC13D gene-associated familial hemophagocytic lymphohistiocytosis triggered by visceral leishmaniasis: a diagnostic challenge.
Gunay Balta, Fatih M Azik, Aytemiz Gurgey

J Pediatr Hematol Oncol· January 2014

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Association of nonimmune hydrops fetalis with familial hemophagocytic lymphohistiocytosis in identical twin neonates with perforin His222Arg (c665A>G) mutation.
Gunay Balta, Sevilay Topcuoglu, Tugba Gursoy, Aytemiz Gurgey, Fahri Ovali

J Pediatr Hematol Oncol· November 2013

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Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis.
Sule Unal, Gunay Balta, Hamza Okur, Selin Aytac, Mualla Cetin

J Pediatr Hematol Oncol· July 2013

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Spinal cord involvement in a child with familial hemophagocytic lymphohistiocytosis.
Muge Gokce, Gunay Balta, Sule Unal, Kader Oguz, Mualla Cetin

J Pediatr Neurosci· September 2012

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Leptin promoter G-2548A genotypes and associated serum leptin levels in childhood acute leukemia at diagnosis and under high-dose steroid therapy.
Betul Tavil, Gunay Balta, Eser Lay Ergun, Serdar Ozkasap, Murat Tuncer

Leuk Lymphoma· April 2012

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The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis.
Hamza Okur, Şule Ünal, Günay Balta, Didem Efendioğlu, Eren Çimen

Turk J Haematol· June 2011

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Hemophagocytic syndrome in a child with severe Crohn's disease and familial Mediterranean fever.
Nuray Uslu, Hulya Demir, Gunay Balta, Inci N Saltik-Temizel, Hasan Ozen

J Crohns Colitis· September 2010

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Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation.
Gunay Balta, Hamza Okur, Sule Unal, Nese Yarali, Adalet Meral Gunes

Leuk Res· August 2010

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Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene.
Ahmet Faik Oner, Hamza Okur, Gunay Balta, Sule Unal, Ibrahim Deger

Leuk Res· September 2009

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Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Orhan Onalan, Gunay Balta, Ali Oto, Giray Kabakci, Lale Tokgozoglu

J Thromb Thrombolysis· December 2008

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Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: reevaluation of fetal hemoglobin values by a sensitive method.
Fatma Gumruk, Betul Tavil, Gunay Balta, Selma Unal, Aytemiz Gurgey

J Pediatr Hematol Oncol· December 2008

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Central nervous system involvement in Turkish children with primary hemophagocytic lymphohistiocytosis.
Aytemiz Gurgey, Selin Aytac, Gunay Balta, Kader K Oguz, Fatma Gumruk

J Child Neurol· November 2008

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Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations.
Hamza Okur, Gunay Balta, Nurten Akarsu, Ahmet Oner, Turkan Patiroglu

Leuk Res· June 2008

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Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
Emel Ozyurek, Gunay Balta, Aydan Degerliyurt, Hülya Parlak, Sabiha Aysun

Clin Appl Thromb Hemost· April 2007

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Analysis of some clinical and laboratory aspects of adolescent patients with thrombosis.
Aytemiz Gurgey, Gunay Balta, Fatma Gumruk, Cigdem Altay

Blood Coagul Fibrinolysis· October 2004

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Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
Selma Unal, Gunay Balta, Feride Duru, Fatma Gumruk, Cigdem Altay

Blood Coagul Fibrinolysis· June 2004

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Molecular characterization of Turkish patients with pyrimidine 5' nucleotidase-I deficiency.
Gunay Balta, Fatma Gumruk, Nurten Akarsu, Aytemiz Gurgey, Cigdem Altay

Blood· September 2003

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Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia.
Gunay Balta, Nazmiye Yuksek, Emel Ozyurek, Ulya Ertem, Gonul Hicsonmez

Am J Hematol· July 2003

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Factor V Leiden mutation and PAI-1 gene 4G/5G genotype in thrombotic patients with Behcet's disease.
Aytemiz Gurgey, Gunay Balta, Ayse Boyvat

Blood Coagul Fibrinolysis· February 2003

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PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs.
Gunay Balta, Cigdem Altay, Aytemiz Gurgey

Am J Hematol· October 2002

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