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Hemoglobin
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April 10, 2012
Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy
Cigdem Karakukcu, Musa Karakukcu, Ekrem Unal, et al.
Leukemia Research
|
January 15, 2008
Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations
Hamza Okur, Gunay Balta, Nurten Akarsu, et al.
Northern Clinics of Istanbul
|
January 29, 2019
Evaluation of childhood solid pseudopapillary tumors of the pancreas
Alper Ozcan, Ceyda Arslanoglu, Ekrem Unal, et al.
The Eurasian Journal of Medicine
|
August 24, 2016
Dermatological Findings in Turkish Paediatric Haematology-Oncology Patients
Umit Uksal, Pinar Ozturk, Emine Colgecen, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 8, 2013
Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86
Mehmet Canpolat, Huseyin Per, Hakan Gumus, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 24, 2012
Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant
Turkan Patiroglu, Dilek Sarici, Ekrem Unal, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 13, 2011
Intracranial hemorrhage in children with congenital factor deficiencies
Turkan Patiroglu, Mehmet Akif Ozdemir, Ekrem Unal, et al.
European Journal of Microbiology & Immunology
|
September 13, 2014
X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report
Turkan Patiroglu, H Haluk Akar, Mirjam van den Burg, et al.
Journal of Clinical Immunology
|
August 9, 2014
Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review
Turkan Patiroglu, H Haluk Akar, Kimberly Gilmour, et al.
Journal of Pediatric Hematology/Oncology
|
March 25, 2020
Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant
Aysenur Paç Kisaarslan, Maximilam Witzel, Ekrem Unal, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 90) with videos related to
Sort By:
Page
of 9
Hemoglobin
|
April 10, 2012
Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy
Cigdem Karakukcu, Musa Karakukcu, Ekrem Unal, et al.
Leukemia Research
|
January 15, 2008
Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations
Hamza Okur, Gunay Balta, Nurten Akarsu, et al.
Northern Clinics of Istanbul
|
January 29, 2019
Evaluation of childhood solid pseudopapillary tumors of the pancreas
Alper Ozcan, Ceyda Arslanoglu, Ekrem Unal, et al.
The Eurasian Journal of Medicine
|
August 24, 2016
Dermatological Findings in Turkish Paediatric Haematology-Oncology Patients
Umit Uksal, Pinar Ozturk, Emine Colgecen, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 8, 2013
Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86
Mehmet Canpolat, Huseyin Per, Hakan Gumus, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 24, 2012
Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant
Turkan Patiroglu, Dilek Sarici, Ekrem Unal, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 13, 2011
Intracranial hemorrhage in children with congenital factor deficiencies
Turkan Patiroglu, Mehmet Akif Ozdemir, Ekrem Unal, et al.
European Journal of Microbiology & Immunology
|
September 13, 2014
X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report
Turkan Patiroglu, H Haluk Akar, Mirjam van den Burg, et al.
Journal of Clinical Immunology
|
August 9, 2014
Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review
Turkan Patiroglu, H Haluk Akar, Kimberly Gilmour, et al.
Journal of Pediatric Hematology/Oncology
|
March 25, 2020
Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant
Aysenur Paç Kisaarslan, Maximilam Witzel, Ekrem Unal, et al.
Page
of 9