Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Tezcan

Showing results (61-70 of 73) with videos related to

Pageof 8
Sort By:
Journal of Investigational Allergology & Clinical Immunology|August 4, 2018
A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin LymphomaB Gokturk, J L Casanova, C Picard, et al.
Bone Marrow Transplantation|July 26, 2016
Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the otherD Çağdaş, B Erman, D Hanoğlu, et al.
Bone Marrow Transplantation|October 12, 1999
Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvementI Tezcan, O Sanal, F Ersoy, et al.
European Annals of Allergy and Clinical Immunology|May 7, 2020
Primary Immunodeficiency Disorders in children with Non-Cystic Fibrosis BronchiectasisD Çağdaş, M Pehlivantürk Kizılkan, A Tagiyev, et al.
European Journal of Clinical Investigation|July 24, 2009
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutationsM Y Köker, O Sanal, K van Leeuwen, et al.
European Journal of Clinical Investigation|March 19, 2009
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous diseaseM Y Köker, K van Leeuwen, M de Boer, et al.
Genomics|March 8, 2000
Two genes are responsible for Griscelli syndrome at the same 15q21 locusE Pastural, F Ersoy, N Yalman, et al.
Blood|December 3, 1998
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantationI Tezcan, W Xu, A Gurgey, et al.
Journal of Clinical Immunology|October 27, 1999
Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasiaO Sanal, F Ersoy, L Yel, et al.
Blood|June 25, 1999
Incomplete T-cell immune reconstitution in two major histocompatibility complex class II-deficiency/bare lymphocyte syndrome patients after HLA-identical sibling bone marrow transplantationB C Godthelp, M C van Eggermond, A Peijnenburg, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Journal of Investigational Allergology & Clinical Immunology|August 4, 2018
A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin LymphomaB Gokturk, J L Casanova, C Picard, et al.
Bone Marrow Transplantation|July 26, 2016
Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the otherD Çağdaş, B Erman, D Hanoğlu, et al.
Bone Marrow Transplantation|October 12, 1999
Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvementI Tezcan, O Sanal, F Ersoy, et al.
European Annals of Allergy and Clinical Immunology|May 7, 2020
Primary Immunodeficiency Disorders in children with Non-Cystic Fibrosis BronchiectasisD Çağdaş, M Pehlivantürk Kizılkan, A Tagiyev, et al.
European Journal of Clinical Investigation|July 24, 2009
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutationsM Y Köker, O Sanal, K van Leeuwen, et al.
European Journal of Clinical Investigation|March 19, 2009
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous diseaseM Y Köker, K van Leeuwen, M de Boer, et al.
Genomics|March 8, 2000
Two genes are responsible for Griscelli syndrome at the same 15q21 locusE Pastural, F Ersoy, N Yalman, et al.
Blood|December 3, 1998
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantationI Tezcan, W Xu, A Gurgey, et al.
Journal of Clinical Immunology|October 27, 1999
Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasiaO Sanal, F Ersoy, L Yel, et al.
Blood|June 25, 1999
Incomplete T-cell immune reconstitution in two major histocompatibility complex class II-deficiency/bare lymphocyte syndrome patients after HLA-identical sibling bone marrow transplantationB C Godthelp, M C van Eggermond, A Peijnenburg, et al.
Pageof 8