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Journal of Thrombosis and Haemostasis : JTH
|
August 18, 2015
Mild hemophilia A patient with novel Pro1809Leu mutation develops an anti-C2 antibody inhibiting allogeneic but not autologous factor VIII activity
K Yada, K Nogami, M Takeyama, et al.
Bioscience, Biotechnology, and Biochemistry
|
July 1, 1997
Effects of medium-chain fatty acids and their acylglycerols on the transport of penicillin V across Caco-2 cell monolayers
M Shima, K Yohdoh, M Yamaguchi, et al.
Journal of Immunological Methods
|
February 8, 1989
A biotin-avidin sandwich ELISA for quantification of intact complement component C9. The sera from hereditary C9 deficient individuals completely lack C9
Y Takata, T Moriyama, Y Fukumori, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1995
[Spinal canal bleeding in hemophilia A]
S Morichika, M Shima, Y Imanaka, et al.
Acta Paediatrica Scandinavica
|
September 1, 1985
Bone gamma-carboxyglutamic acid containing protein in the perinatal period
M Shima, Y Seino, Y Tanaka, et al.
Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society
|
November 1, 1985
[Multimeric composition of factor VIII-related protein following DDAVP infusion in normal subjects and patients with hemophilia A and von Willebrand's disease]
T Takase, M Nishino, M Yasui, et al.
Thrombosis and Haemostasis
|
April 9, 2011
Mechanisms of human neutrophil elastase-catalysed inactivation of factor VIII(a)
K Nogami, K Ogiwara, T Matsumoto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 30, 2016
The utility of VWF multimer analysis in response to the desmopressin administration for the diagnosis of severe type 1 von Willebrand disease
M Takeyama, K Nogami, M Onaka, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 30, 2014
Comprehensive evaluation of haemostatic function in von Willebrand disease patients using a microchip-based flow chamber system
K Ogiwara, K Nogami, K Hosokawa, et al.
Clinical Orthopaedics and Related Research
|
July 1, 1980
Multiple exostoses--mental retardation (MEMR) syndrome: report of a case
T Miki, H Kohno, H Miyata, et al.
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of 27
Search research articles
Search
Showing results (111-120 of 262) with videos related to
Sort By:
Page
of 27
Journal of Thrombosis and Haemostasis : JTH
|
August 18, 2015
Mild hemophilia A patient with novel Pro1809Leu mutation develops an anti-C2 antibody inhibiting allogeneic but not autologous factor VIII activity
K Yada, K Nogami, M Takeyama, et al.
Bioscience, Biotechnology, and Biochemistry
|
July 1, 1997
Effects of medium-chain fatty acids and their acylglycerols on the transport of penicillin V across Caco-2 cell monolayers
M Shima, K Yohdoh, M Yamaguchi, et al.
Journal of Immunological Methods
|
February 8, 1989
A biotin-avidin sandwich ELISA for quantification of intact complement component C9. The sera from hereditary C9 deficient individuals completely lack C9
Y Takata, T Moriyama, Y Fukumori, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1995
[Spinal canal bleeding in hemophilia A]
S Morichika, M Shima, Y Imanaka, et al.
Acta Paediatrica Scandinavica
|
September 1, 1985
Bone gamma-carboxyglutamic acid containing protein in the perinatal period
M Shima, Y Seino, Y Tanaka, et al.
Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society
|
November 1, 1985
[Multimeric composition of factor VIII-related protein following DDAVP infusion in normal subjects and patients with hemophilia A and von Willebrand's disease]
T Takase, M Nishino, M Yasui, et al.
Thrombosis and Haemostasis
|
April 9, 2011
Mechanisms of human neutrophil elastase-catalysed inactivation of factor VIII(a)
K Nogami, K Ogiwara, T Matsumoto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 30, 2016
The utility of VWF multimer analysis in response to the desmopressin administration for the diagnosis of severe type 1 von Willebrand disease
M Takeyama, K Nogami, M Onaka, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 30, 2014
Comprehensive evaluation of haemostatic function in von Willebrand disease patients using a microchip-based flow chamber system
K Ogiwara, K Nogami, K Hosokawa, et al.
Clinical Orthopaedics and Related Research
|
July 1, 1980
Multiple exostoses--mental retardation (MEMR) syndrome: report of a case
T Miki, H Kohno, H Miyata, et al.
Page
of 27