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Thrombosis and Haemostasis
|
April 20, 2001
Hypofibrinogenemia due to novel 316 Asp --> Tyr substitution in the fibrinogen Bbeta chain
S O Brennan, J M Wyatt, S May, et al.
Annals of the New York Academy of Sciences
|
July 20, 2001
Genetic and immunological characterization of fibrinogen inclusion bodies in patients with hepatic fibrinogen storage and liver disease
D Medicina, G Fabbretti, S O Brennan, et al.
Chemico-Biological Interactions
|
July 27, 1999
Catalytic parameters for the hydrolysis of butyrylthiocholine by human serum butyrylcholinesterase variants
V Simeon-Rudolf, E Reiner, R T Evans, et al.
Lancet (London, England)
|
December 22, 1984
A genetically engineered mutant of alpha 1-antitrypsin protects connective tissue from neutrophil damage and may be useful in lung disease
P M George, M C Vissers, J Travis, et al.
Journal of Clinical Pathology
|
February 1, 1996
Comparison of histological and biochemical hepatic iron indexes in the diagnosis of genetic haemochromatosis
P M George, C Conaghan, H B Angus, et al.
Pathology
|
January 1, 1991
Functional antithrombin-III variant (41 Pro----Leu) identified by liquid secondary ion mass spectrometry
S O Brennan, J Y Borg, G J Shaw, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Novel Aalpha chain truncation (fibrinogen Perth) resulting in low expression and impaired fibrinogen polymerization
V M Homer, J L Mullin, S O Brennan, et al.
Haematologica
|
November 21, 2007
Acquired dysfibrinogenemia caused by monoclonal production of immunoglobulin lambda light chain
A Dear, S O Brennan, M J Sheat, et al.
Pathology
|
October 31, 2015
Evaluation of Abbott Architect high-sensitivity troponin I assay for haemolysis interference
J B Ryan, J Wallace, C W Sies, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
April 7, 2009
Dietary and supplementary betaine: effects on betaine and homocysteine concentrations in males
W Atkinson, S Slow, J Elmslie, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 165) with videos related to
Sort By:
Page
of 17
Thrombosis and Haemostasis
|
April 20, 2001
Hypofibrinogenemia due to novel 316 Asp --> Tyr substitution in the fibrinogen Bbeta chain
S O Brennan, J M Wyatt, S May, et al.
Annals of the New York Academy of Sciences
|
July 20, 2001
Genetic and immunological characterization of fibrinogen inclusion bodies in patients with hepatic fibrinogen storage and liver disease
D Medicina, G Fabbretti, S O Brennan, et al.
Chemico-Biological Interactions
|
July 27, 1999
Catalytic parameters for the hydrolysis of butyrylthiocholine by human serum butyrylcholinesterase variants
V Simeon-Rudolf, E Reiner, R T Evans, et al.
Lancet (London, England)
|
December 22, 1984
A genetically engineered mutant of alpha 1-antitrypsin protects connective tissue from neutrophil damage and may be useful in lung disease
P M George, M C Vissers, J Travis, et al.
Journal of Clinical Pathology
|
February 1, 1996
Comparison of histological and biochemical hepatic iron indexes in the diagnosis of genetic haemochromatosis
P M George, C Conaghan, H B Angus, et al.
Pathology
|
January 1, 1991
Functional antithrombin-III variant (41 Pro----Leu) identified by liquid secondary ion mass spectrometry
S O Brennan, J Y Borg, G J Shaw, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Novel Aalpha chain truncation (fibrinogen Perth) resulting in low expression and impaired fibrinogen polymerization
V M Homer, J L Mullin, S O Brennan, et al.
Haematologica
|
November 21, 2007
Acquired dysfibrinogenemia caused by monoclonal production of immunoglobulin lambda light chain
A Dear, S O Brennan, M J Sheat, et al.
Pathology
|
October 31, 2015
Evaluation of Abbott Architect high-sensitivity troponin I assay for haemolysis interference
J B Ryan, J Wallace, C W Sies, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
April 7, 2009
Dietary and supplementary betaine: effects on betaine and homocysteine concentrations in males
W Atkinson, S Slow, J Elmslie, et al.
Page
of 17