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I Tezcan

Showing results (41-50 of 73) with videos related to

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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 purpuraO 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 periodontitisO 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 amyloidosisI 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 reportN 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 treatmentH 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 casesI Tezcan, M Tuncer, D Uçkan, et al.
Pediatric Transplantation|September 19, 2001
Pneumatosis intestinalis in an infant undergoing bone marrow transplantation for Wiskott-Aldrich syndromeD 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 BMTI 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 agammaglobulinemiaY Wang, H Kanegane, O Sanal, et al.
European Journal of Clinical Investigation|June 20, 2007
Mutations of chronic granulomatous disease in Turkish familiesM Y Köker, O Sanal, M De Boer, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 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 purpuraO 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 periodontitisO 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 amyloidosisI 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 reportN 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 treatmentH 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 casesI Tezcan, M Tuncer, D Uçkan, et al.
Pediatric Transplantation|September 19, 2001
Pneumatosis intestinalis in an infant undergoing bone marrow transplantation for Wiskott-Aldrich syndromeD 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 BMTI 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 agammaglobulinemiaY Wang, H Kanegane, O Sanal, et al.
European Journal of Clinical Investigation|June 20, 2007
Mutations of chronic granulomatous disease in Turkish familiesM Y Köker, O Sanal, M De Boer, et al.
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