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Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1995
Selective IgA deficiency with unusual features: development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura
O Sanal, F Ersoy, A Metin, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 25, 2013
Association of interleukin-1 beta (+3954) gene polymorphism and gingival crevicular fluid levels in patients with aggressive and chronic periodontitis
O Ozer Yücel, E Berker, L Mescil, et al.
Archives of Disease in Childhood
|
October 15, 1998
A case of X linked agammaglobulinaemia complicated with systemic amyloidosis
I Tezcan, F Ersoy, O Sanal, et al.
Australian Dental Journal
|
August 1, 1993
Periodical gingival bleeding as a presenting symptom of periodontitis due to underlying cyclic neutropenia. Case report
N Yamalik, E Yavuzyilmaz, F Cağlayan, et al.
Australian Dental Journal
|
May 16, 1998
A case of chronic severe neutropenia: oral findings and consequences of short-term granulocyte colony-stimulating factor treatment
H Hastürk, I Tezcan, L Yel, et al.
Pediatric Transplantation
|
March 20, 1999
Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases
I Tezcan, M Tuncer, D Uçkan, et al.
Pediatric Transplantation
|
September 19, 2001
Pneumatosis intestinalis in an infant undergoing bone marrow transplantation for Wiskott-Aldrich syndrome
D Uçkan, M Cetin, M Haliloglu, et al.
Pediatric Hematology and Oncology
|
October 23, 1998
Necrotizing otitis externa, otitis media, peripheral facial paralysis, and brain abscess in a thalassemic child after allogeneic BMT
I Tezcan, A M Tuncer, I Yenicesu, et al.
Human Mutation
|
October 23, 2001
Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia
Y Wang, H Kanegane, O Sanal, et al.
European Journal of Clinical Investigation
|
June 20, 2007
Mutations of chronic granulomatous disease in Turkish families
M Y Köker, O Sanal, M De Boer, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 73) with videos related to
Sort By:
Page
of 8
Acta Paediatrica Japonica : Overseas Edition
|
August 1, 1995
Selective IgA deficiency with unusual features: development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura
O Sanal, F Ersoy, A Metin, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 25, 2013
Association of interleukin-1 beta (+3954) gene polymorphism and gingival crevicular fluid levels in patients with aggressive and chronic periodontitis
O Ozer Yücel, E Berker, L Mescil, et al.
Archives of Disease in Childhood
|
October 15, 1998
A case of X linked agammaglobulinaemia complicated with systemic amyloidosis
I Tezcan, F Ersoy, O Sanal, et al.
Australian Dental Journal
|
August 1, 1993
Periodical gingival bleeding as a presenting symptom of periodontitis due to underlying cyclic neutropenia. Case report
N Yamalik, E Yavuzyilmaz, F Cağlayan, et al.
Australian Dental Journal
|
May 16, 1998
A case of chronic severe neutropenia: oral findings and consequences of short-term granulocyte colony-stimulating factor treatment
H Hastürk, I Tezcan, L Yel, et al.
Pediatric Transplantation
|
March 20, 1999
Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases
I Tezcan, M Tuncer, D Uçkan, et al.
Pediatric Transplantation
|
September 19, 2001
Pneumatosis intestinalis in an infant undergoing bone marrow transplantation for Wiskott-Aldrich syndrome
D Uçkan, M Cetin, M Haliloglu, et al.
Pediatric Hematology and Oncology
|
October 23, 1998
Necrotizing otitis externa, otitis media, peripheral facial paralysis, and brain abscess in a thalassemic child after allogeneic BMT
I Tezcan, A M Tuncer, I Yenicesu, et al.
Human Mutation
|
October 23, 2001
Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia
Y Wang, H Kanegane, O Sanal, et al.
European Journal of Clinical Investigation
|
June 20, 2007
Mutations of chronic granulomatous disease in Turkish families
M Y Köker, O Sanal, M De Boer, et al.
Page
of 8