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British Journal of Haematology|July 27, 2001
Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X-linked agammaglobulinaemia and carrier femalesT Futatani, C Watanabe, Y Baba, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|March 11, 1998
[The oldest case with X-linked agammaglobulinemia in Japan lacking Bruton-type tyrosine kinase protein detected by flow cytometry]F Ishida, H Kobayashi, H Saito, et al.Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|January 30, 2002
Survival of wild polio by a patient with XLASampson Sarpong, Helen S Skolnick, Hans D Ochs, 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.Pediatric Surgery International|June 18, 2003
A case of body stalk anomaly arising in the second baby of a triplet pregnancy after in-vitro fertilization and embryo transferS Hirokawa, H Uotani, T Futatani, et al.The Journal of Allergy and Clinical Immunology|December 14, 2001
Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysisH Kanegane, T Futatani, Y Wang, et al.Genes and Immunity|September 21, 2007
Novel mutations in a Japanese patient with CD19 deficiencyH Kanegane, K Agematsu, T Futatani, et al.Clinical and Experimental Immunology|June 9, 2000
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency RegistryH Kanegane, S Tsukada, T Iwata, et al.Pediatric Research|January 3, 2001
Neutrophils and mononuclear cells express vascular endothelial growth factor in acute Kawasaki disease: its possible role in progression of coronary artery lesionsY Hamamichi, F Ichida, X Yu, et al.Internal Medicine (Tokyo, Japan)|September 10, 1999
Atypical X-linked agammaglobulinemia diagnosed in three adultsS Hashimoto, T Miyawaki, T Futatani, et al.Pageof 2