Berna Atabay

MUTATION OF THE PROTON-COUPLED FOLATE TRANSPORTER GENE (PCFT-SLC46A1) IN TURKISH SIBLINGS WITH HEREDITARY FOLATE MALABSORPTION

Berna Atabay, Meral Türker, Esra Arun Özer et al. · Pediatric Hematology and Oncology · 2010 · 28 citations · Full text

Genetics, Genetic Epidemiology, Molecular Biology +16

Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

Deniz Yılmaz Karapınar, Türkan Patıroğlu, Ayşe Metìn et al. · Pediatric Blood & Cancer · 2019 · 25 citations

Investigation of megakaryocyte apoptosis in children with acute and chronic idiopathic thrombocytopenic purpura

Canan Uçar, Hale Ören, Gülersu i ̇rken et al. · European Journal Of Haematology · 2003 · 19 citations

Life-Threatening Mediastinal-Retroperitoneal Hemorrhage in a Child With Moderate Hemophilia A and High Inhibitor Titer

Şebnem Ylmaz, Hale Ören, Gülersu İrken et al. · Journal of Pediatric Hematology/Oncology · 2005 · 15 citations

Gastroenterology, Surgery, Factor Iii Inhibitor +16

Treatment outcome of adolescents with acute lymphoblastic leukemia

G Irken, Hale Ören, Hüseyin Gülen et al. · Annals of Hematology · 2002 · 15 citations

Hematological Malignancy, Oncology, Pediatric Hematology +5