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R Pflugshaupt

Showing results (1-10 of 11) with videos related to

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Vox Sanguinis|January 1, 1983
FPA content - a criterion of quality for plasma as factor VIII sourceR Pflugshaupt, G Kurt
Human Heredity|January 1, 1981
Isoelectric focusing of human red cell phosphoglucomutase (PGM1): phenotype distribution in the Swiss population - rare phenotypesR Scherz, R Pflugshaupt, R Bütler
Vox Sanguinis|January 1, 1977
Naturally occurring human antibodies with specificity for light chains of immunoglobulinsR Scherz, R Pflugshaupt, R Bütler
Human Genetics|November 24, 1978
A new rare phenotype of glycine-rich beta-glycoproteinR Scherz, R Pflugshaupt, R Bütler
Human Genetics|December 29, 1976
A new genetic variant of galactose-1-phosphate uridyl transferaseR Scherz, R Pflugshaupt, R Bütler
Human Heredity|January 1, 1982
Genetic polymorphism of glycine-rich beta-glycoprotein in the Italian populationR Scherz, R Pflugshaupt, R Bütler, et al.
Vox Sanguinis|July 1, 1978
Variable degradation of factor VIII-related protein in lyophilised concentrates of antihaemophilic factor (AHF)T Jakab, R Pflugshaupt, M Furlan, et al.
Thrombosis Research|June 15, 1992
Multimeric analysis of von Willebrand factor by vertical sodium dodecyl sulphate agarose gel electrophoresis, vacuum blotting technology and sensitive visualization by alkaline phosphatase anti-alkaline phosphatase complexP Baillod, B Affolter, G H Kurt, et al.
American Journal of Hematology|May 1, 1995
New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding historyP Baillod, C Gaucher, B Affolter, et al.
American Journal of Physical Anthropology|August 1, 1988
Study of five haemogenetic markers (Gc, C3, Bf, Ag, and GALT) in six Indonesian populations and in 12 subgroups of BalineseR Scherz, G Breguet, R Ney, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Vox Sanguinis|January 1, 1983
FPA content - a criterion of quality for plasma as factor VIII sourceR Pflugshaupt, G Kurt
Human Heredity|January 1, 1981
Isoelectric focusing of human red cell phosphoglucomutase (PGM1): phenotype distribution in the Swiss population - rare phenotypesR Scherz, R Pflugshaupt, R Bütler
Vox Sanguinis|January 1, 1977
Naturally occurring human antibodies with specificity for light chains of immunoglobulinsR Scherz, R Pflugshaupt, R Bütler
Human Genetics|November 24, 1978
A new rare phenotype of glycine-rich beta-glycoproteinR Scherz, R Pflugshaupt, R Bütler
Human Genetics|December 29, 1976
A new genetic variant of galactose-1-phosphate uridyl transferaseR Scherz, R Pflugshaupt, R Bütler
Human Heredity|January 1, 1982
Genetic polymorphism of glycine-rich beta-glycoprotein in the Italian populationR Scherz, R Pflugshaupt, R Bütler, et al.
Vox Sanguinis|July 1, 1978
Variable degradation of factor VIII-related protein in lyophilised concentrates of antihaemophilic factor (AHF)T Jakab, R Pflugshaupt, M Furlan, et al.
Thrombosis Research|June 15, 1992
Multimeric analysis of von Willebrand factor by vertical sodium dodecyl sulphate agarose gel electrophoresis, vacuum blotting technology and sensitive visualization by alkaline phosphatase anti-alkaline phosphatase complexP Baillod, B Affolter, G H Kurt, et al.
American Journal of Hematology|May 1, 1995
New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding historyP Baillod, C Gaucher, B Affolter, et al.
American Journal of Physical Anthropology|August 1, 1988
Study of five haemogenetic markers (Gc, C3, Bf, Ag, and GALT) in six Indonesian populations and in 12 subgroups of BalineseR Scherz, G Breguet, R Ney, et al.
Pageof 2