The Relationship Between Hematological Findings and Coronary Artery Aneurysm in Kawasaki Disease

por Beken, Burçin, Ünal, Şule, Çetin, Mualla, Gümrük, Fatma
Publicado 2014

Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the L...

por Bayhan, Turan, Ünal, Şule, Gümrük, Fatma, Çetin, Mualla
Publicado 2015

Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease

por Sayın, Seçil, Ünal, Şule, Çetin, Mualla, Gümrük, Fatma
Publicado 2019

Reliability and Validity of the Turkish Version of the PedsQL 3.0 Cancer Module for 2- to 7-Year-Old and the PedsQL 4.0 Generic Core Scales for 5- to 7-Year-Old: The Hacettepe Univ...

por Yıldız Kabak, Vesile, Yakut, Yavuz, Çetin, Mualla, Düger, Tülin
Publicado 2016

Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

por Bozkurt, Süreyya, Ünal, Şule, Bayhan, Turan, Gümrük, Fatma, Çetin, Mualla
Publicado 2020

Hematological features in children with systemic lupus erythematosus: are they more common than appreciated?

por Gokce, Muge, Besbas, Nesrin, Bilginer, Yelda, Cetin, Mualla, Gumruk, Fatma, Ozen, Seza
Publicado 2011

Spinal cord involvement in a child with familial hemophagocytic lymphohistiocytosis

por Gokce, Muge, Balta, Gunay, Unal, Sule, Oguz, Kader, Cetin, Mualla, Gumruk, Fatma
Publicado 2012

Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant

por Gökçe, Müge, Aytaç, Selin, Ünal, Şule, Altan, İlhan, Gümrük, Fatma, Çetin, Mualla
Publicado 2015

Intracerebral metastasis in pediatric acute lymphoblastic leukemia: A rare presentation

por Gokce, Müge, Aytac, Selin, Altan, Ilhan, Unal, Sule, Tuncer, Murat, Gumruk, Fatma, Cetin, Mualla
Publicado 2012

Transcobalamin II Deficiency in Four Cases with Novel Mutations

por Ünal, Şule, Rupar, Tony, Yetgin, Sevgi, Yaralı, Neşe, Dursun, Ali, Gürsel, Türkiz, Çetin, Mualla
Publicado 2015

The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience

por Beken, Burcin, Aytac, Selin, Balta, Gunay, Kuskonmaz, Baris, Uckan, Duygu, Unal, Sule, Cetin, Mualla, Gumruk, Fatma
Publicado 2018

Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases

por Fermo, Elisa, Vercellati, Cristina, Marcello, Anna Paola, Zaninoni, Anna, Aytac, Selin, Cetin, Mualla, Capolsini, Ilaria, Casale, Maddalena, Paci, Sabrina, Zanella, Alberto, Barcellini, Wilma, Bianchi, Paola
Publicado 2019

NBEAL2 is mutated in Gray Platelet Syndrome and is required for biogenesis of platelet alpha-granules

por Gunay-Aygun, Meral, Falik-Zaccai, Tzipora C, Vilboux, Thierry, Zivony-Elboum, Yifat, Gumruk, Fatma, Cetin, Mualla, Khayat, Morad, Boerkoel, Cornelius F, Kfir, Nehama, Huang, Yan, Maynard, Dawn, Dorward, Heidi, Berger, Katherine, Kleta, Robert, Anikster, Yair, Arat, Mutlu, Freiberg, Andrew S, Kehrel, Beate E, Jurk, Kerstin, Cruz, Pedro, Mullikin, Jim C, White, James G, Huizing, Marjan, Gahl, William A
Publicado 2011