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The Lancet. Respiratory Medicine
|
September 19, 2017
Predictors of enhanced response with benralizumab for patients with severe asthma: pooled analysis of the SIROCCO and CALIMA studies
J Mark FitzGerald, Eugene R Bleecker, Andrew Menzies-Gow, et al.
JMIR Formative Research
|
June 22, 2023
Identifying Patient Populations in Texts Describing Drug Approvals Through Deep Learning-Based Information Extraction: Development of a Natural Language Processing Algorithm
Aline Gendrin, Leonidas Souliotis, James Loudon-Griffiths, et al.
Thrombosis and Haemostasis
|
August 9, 2006
Establishment of the 1st International Genetic Reference Panel for Factor V Leiden, human gDNA
Elaine Gray, J Ross Hawkins, Marion Morrison, et al.
Transfusion
|
June 22, 2007
HPA-1a antibody potency and bioactivity do not predict severity of fetomaternal alloimmune thrombocytopenia
Cedric Ghevaert, Kate Campbell, Prachi Stafford, et al.
Transfusion
|
February 27, 2007
Molecular characterization of the variable domains of an alphaIIbbeta3-specific immunoglobulin M kappa platelet cold agglutinin in a follicular lymphoma patient with treatment refractory autoimmune thrombocytopenia: idiotypic overlap between alphaIIbbeta3 integrin antibodies
Nicola S Jennings, Ian J Harmer, Kate Campbell, et al.
European Journal of Human Genetics : EJHG
|
May 19, 2011
Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes
Jennifer Boyle, Malcolm Hawkins, David E Barton, et al.
Blood
|
February 28, 2002
A tyrosine703serine polymorphism of CD109 defines the Gov platelet alloantigens
Andre C Schuh, Nick A Watkins, Quang Nguyen, et al.
Blood
|
February 28, 2002
HPA-1a phenotype-genotype discrepancy reveals a naturally occurring Arg93Gln substitution in the platelet beta 3 integrin that disrupts the HPA-1a epitope
Nicholas A Watkins, Elisabeth Schaffner-Reckinger, David L Allen, et al.
European Journal of Human Genetics : EJHG
|
August 26, 2010
Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome
Malcolm Hawkins, Jennifer Boyle, Kathleen E Wright, et al.
Transfusion
|
July 16, 2015
A multicenter validation of recombinant β3 integrin-coupled beads to detect human platelet antigen-1 alloantibodies in 498 cases of fetomaternal alloimmune thrombocytopenia
Winnie Chong, Ernest Turro, Paul Metcalfe, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
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The Lancet. Respiratory Medicine
|
September 19, 2017
Predictors of enhanced response with benralizumab for patients with severe asthma: pooled analysis of the SIROCCO and CALIMA studies
J Mark FitzGerald, Eugene R Bleecker, Andrew Menzies-Gow, et al.
JMIR Formative Research
|
June 22, 2023
Identifying Patient Populations in Texts Describing Drug Approvals Through Deep Learning-Based Information Extraction: Development of a Natural Language Processing Algorithm
Aline Gendrin, Leonidas Souliotis, James Loudon-Griffiths, et al.
Thrombosis and Haemostasis
|
August 9, 2006
Establishment of the 1st International Genetic Reference Panel for Factor V Leiden, human gDNA
Elaine Gray, J Ross Hawkins, Marion Morrison, et al.
Transfusion
|
June 22, 2007
HPA-1a antibody potency and bioactivity do not predict severity of fetomaternal alloimmune thrombocytopenia
Cedric Ghevaert, Kate Campbell, Prachi Stafford, et al.
Transfusion
|
February 27, 2007
Molecular characterization of the variable domains of an alphaIIbbeta3-specific immunoglobulin M kappa platelet cold agglutinin in a follicular lymphoma patient with treatment refractory autoimmune thrombocytopenia: idiotypic overlap between alphaIIbbeta3 integrin antibodies
Nicola S Jennings, Ian J Harmer, Kate Campbell, et al.
European Journal of Human Genetics : EJHG
|
May 19, 2011
Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes
Jennifer Boyle, Malcolm Hawkins, David E Barton, et al.
Blood
|
February 28, 2002
A tyrosine703serine polymorphism of CD109 defines the Gov platelet alloantigens
Andre C Schuh, Nick A Watkins, Quang Nguyen, et al.
Blood
|
February 28, 2002
HPA-1a phenotype-genotype discrepancy reveals a naturally occurring Arg93Gln substitution in the platelet beta 3 integrin that disrupts the HPA-1a epitope
Nicholas A Watkins, Elisabeth Schaffner-Reckinger, David L Allen, et al.
European Journal of Human Genetics : EJHG
|
August 26, 2010
Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome
Malcolm Hawkins, Jennifer Boyle, Kathleen E Wright, et al.
Transfusion
|
July 16, 2015
A multicenter validation of recombinant β3 integrin-coupled beads to detect human platelet antigen-1 alloantibodies in 498 cases of fetomaternal alloimmune thrombocytopenia
Winnie Chong, Ernest Turro, Paul Metcalfe, et al.
Page
of 3