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Sule Unal

Showing results (71-80 of 105) with videos related to

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Pediatric Blood & Cancer|October 12, 2013
A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal periodSule Unal, Fatma Gumruk, Sule Yigit, et al.
Pediatric Hematology and Oncology|August 4, 2010
Fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin (FLAG-IDA) for the treatment of children with poor-prognosis acute leukemia: the Hacettepe experienceBetul Tavil, Selin Aytac, Yasemin Isik Balci, et al.
Frontiers in Physiology|August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Leukemia Research|June 17, 2014
Number of erythrocyte transfusions is more predictive than serum ferritin in estimation of cardiac iron loading in pediatric patients with acute lymphoblastic leukemiaSule Unal, Mualla Cetin, Tuncay Hazirolan, et al.
Frontiers in Physiology|June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Blood Advances|March 16, 2018
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopeniaManuela Germeshausen, Phil Ancliff, Jaime Estrada, et al.
Leukemia Research|March 4, 2010
Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutationGunay Balta, Hamza Okur, Sule Unal, et al.
Thrombosis Research|August 25, 2014
Bleeding and non-bleeding phenotypes in patients with GGCX gene mutationsMatthias Watzka, Christof Geisen, Monika Scheer, et al.
Pediatric Blood & Cancer|October 10, 2013
Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesisSule Unal, Yasemin Alanay, Mualla Cetin, et al.
Pageof 11

Showing results (71-80 of 105) with videos related to

Sort By:
Pageof 11
Pediatric Blood & Cancer|October 12, 2013
A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal periodSule Unal, Fatma Gumruk, Sule Yigit, et al.
Pediatric Hematology and Oncology|August 4, 2010
Fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin (FLAG-IDA) for the treatment of children with poor-prognosis acute leukemia: the Hacettepe experienceBetul Tavil, Selin Aytac, Yasemin Isik Balci, et al.
Frontiers in Physiology|August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Leukemia Research|June 17, 2014
Number of erythrocyte transfusions is more predictive than serum ferritin in estimation of cardiac iron loading in pediatric patients with acute lymphoblastic leukemiaSule Unal, Mualla Cetin, Tuncay Hazirolan, et al.
Frontiers in Physiology|June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Blood Advances|March 16, 2018
MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopeniaManuela Germeshausen, Phil Ancliff, Jaime Estrada, et al.
Leukemia Research|March 4, 2010
Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutationGunay Balta, Hamza Okur, Sule Unal, et al.
Thrombosis Research|August 25, 2014
Bleeding and non-bleeding phenotypes in patients with GGCX gene mutationsMatthias Watzka, Christof Geisen, Monika Scheer, et al.
Pediatric Blood & Cancer|October 10, 2013
Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesisSule Unal, Yasemin Alanay, Mualla Cetin, et al.
Pageof 11