Gülen Tüysüz

Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL.

Yücel Erbilgin, Müge Sayitoğlu, Ömer Doğru et al. · PubMed · 2010 · 33 citations · Full text

Lymphocyte Development, Genetics, Immunology +18

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

Prognostic Significance of<i>NOTCH1</i>and<i>FBXW7</i>Mutations in Pediatric T-ALL

Yücel Erbilgin, Müge Sayitoğlu, Ömer Doğru et al. · Disease Markers · 2010 · 23 citations · Full text

Lymphocyte Development, Genetics, Immunology +17

Febrile neutropenia in children with acute lymphoblastic leukemia: single center experience

Nihal Özdemir, Gülen Tüysüz, Nigar Çelik et al. · Türk Pediatri Arşivi · 2016 · 20 citations · Full text

Health-related Quality of Life and its Predictors Among Transfusion-dependent Thalassemia Patients

Gülen Tüysüz, Funda Tayfun · Journal of Pediatric Hematology/Oncology · 2017 · 18 citations