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Sule Unal

Showing results (51-60 of 114) with videos related to

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Leukemia Research|May 26, 2009
Disease causing nature of homozygous missense, p.A523D, alteration in the perforin geneAhmet Faik Oner, Hamza Okur, Gunay Balta, et al.
Journal of Child Neurology|March 29, 2005
Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletionSule Unal, H Serap Kalkanoğlu, Cetin Kocaefe, et al.
Hemoglobin|January 10, 2015
The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patientSule Unal, David H K Chui, Hong-Yuan Luo, et al.
The Turkish Journal of Pediatrics|May 4, 2011
An unexpected parasitic cause of hypereosinophilia: fascioliasisMüge Gökçe, Umit Sahiner, Sule Unal, et al.
Haematologica|November 18, 2017
The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experienceBurcin Beken, Selin Aytac, Gunay Balta, et al.
The Turkish Journal of Pediatrics|October 13, 2009
Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from TurkeyTiraje Celkan, Su Berrak, Elif Kazanci, et al.
Journal of Pediatric Hematology/Oncology|January 1, 2013
Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritisSule Unal, Gunay Balta, Hamza Okur, et al.
The Turkish Journal of Pediatrics|March 9, 2012
A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosisMüge Gökçe, Sule Unal, Hayriye Gülşen, et al.
Pediatric Hematology and Oncology|July 10, 2010
Deferasirox use after hematopoietic stem cell transplantation in pediatric patients with beta-thalassemia major: preliminary resultsSule Unal, Baris Kuskonmaz, Tuncay Hazirolan, et al.
Frontiers in Physiology|June 28, 2021
Proerythroblast Cells of Diamond-Blackfan Anemia Patients With <i>RPS19</i> and <i>CECR1</i> Mutations Have Similar Transcriptomic SignatureBeren Karaosmanoglu, M Alper Kursunel, Duygu Uckan Cetinkaya, et al.
Pageof 12

Showing results (51-60 of 114) with videos related to

Sort By:
Pageof 12
Leukemia Research|May 26, 2009
Disease causing nature of homozygous missense, p.A523D, alteration in the perforin geneAhmet Faik Oner, Hamza Okur, Gunay Balta, et al.
Journal of Child Neurology|March 29, 2005
Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletionSule Unal, H Serap Kalkanoğlu, Cetin Kocaefe, et al.
Hemoglobin|January 10, 2015
The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patientSule Unal, David H K Chui, Hong-Yuan Luo, et al.
The Turkish Journal of Pediatrics|May 4, 2011
An unexpected parasitic cause of hypereosinophilia: fascioliasisMüge Gökçe, Umit Sahiner, Sule Unal, et al.
Haematologica|November 18, 2017
The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experienceBurcin Beken, Selin Aytac, Gunay Balta, et al.
The Turkish Journal of Pediatrics|October 13, 2009
Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from TurkeyTiraje Celkan, Su Berrak, Elif Kazanci, et al.
Journal of Pediatric Hematology/Oncology|January 1, 2013
Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritisSule Unal, Gunay Balta, Hamza Okur, et al.
The Turkish Journal of Pediatrics|March 9, 2012
A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosisMüge Gökçe, Sule Unal, Hayriye Gülşen, et al.
Pediatric Hematology and Oncology|July 10, 2010
Deferasirox use after hematopoietic stem cell transplantation in pediatric patients with beta-thalassemia major: preliminary resultsSule Unal, Baris Kuskonmaz, Tuncay Hazirolan, et al.
Frontiers in Physiology|June 28, 2021
Proerythroblast Cells of Diamond-Blackfan Anemia Patients With <i>RPS19</i> and <i>CECR1</i> Mutations Have Similar Transcriptomic SignatureBeren Karaosmanoglu, M Alper Kursunel, Duygu Uckan Cetinkaya, et al.
Pageof 12