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Alan T Nurden

Showing results (61-70 of 109) with videos related to

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Thrombosis and Haemostasis|January 31, 2014
Phosphatidylserine exposure, microparticle formation and mitochondrial depolarisation in Glanzmann thrombasthenia plateletsHong Wang, K W Annie Bang, Victor S Blanchette, et al.
Haematologica|July 18, 2009
Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor genePaquita Nurden, Alan T Nurden, Silvia La Marca, et al.
Thrombosis and Haemostasis|July 10, 2008
Phenotypic heterogeneity in the Gray platelet syndrome extends to the expression of TREM family member, TLT-1Alan T Nurden, Paquita Nurden, Emilsé Bermejo, et al.
Thrombosis and Haemostasis|October 4, 2002
Analysis of the amino acid requirement for a normal alphaIIbbeta3 maturation at alphaIIbGlu324 commonly mutated in Glanzmann thrombastheniaSandrine Milet-Marsal, Christelle Breillat, Olivier Peyruchaud, et al.
Platelets|March 19, 2002
A novel 196Leu to Pro substitution in the beta3 subunit of the alphaIIbbeta3 integrin in a patient with a variant form of Glanzmann thrombastheniaAlan T Nurden, Jian Ruan, Jean-Max Pasquet, et al.
Thrombosis and Haemostasis|October 7, 2004
Delayed immunologic thrombocytopenia induced by abciximabPaquita Nurden, Gisèle Clofent-Sanchez, Catherine Jais, et al.
Thrombosis and Haemostasis|May 29, 2010
Development of a high-throughput ELISA assay for platelet function testing using platelet-rich plasma or whole bloodIsabelle Salles, Katleen Broos, Alexandre Fontayne, et al.
Plastic and Reconstructive Surgery|February 22, 2007
Reciprocal actions of platelet-secreted TGF-beta1 on the production of VEGF and HGF by human tendon cellsEduardo Anitua, Mikel Sanchez, Alan T Nurden, et al.
Thrombosis and Haemostasis|September 6, 2006
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptideLysiane Hilbert, Paquita Nurden, Claudine Caron, et al.
Haematologica|February 14, 2018
A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of <i>ITGB3</i>: evidence of a dominant effect of gain-of-function mutationsLoredana Bury, Eva Zetterberg, Eva B Leinøe, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
Thrombosis and Haemostasis|January 31, 2014
Phosphatidylserine exposure, microparticle formation and mitochondrial depolarisation in Glanzmann thrombasthenia plateletsHong Wang, K W Annie Bang, Victor S Blanchette, et al.
Haematologica|July 18, 2009
Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor genePaquita Nurden, Alan T Nurden, Silvia La Marca, et al.
Thrombosis and Haemostasis|July 10, 2008
Phenotypic heterogeneity in the Gray platelet syndrome extends to the expression of TREM family member, TLT-1Alan T Nurden, Paquita Nurden, Emilsé Bermejo, et al.
Thrombosis and Haemostasis|October 4, 2002
Analysis of the amino acid requirement for a normal alphaIIbbeta3 maturation at alphaIIbGlu324 commonly mutated in Glanzmann thrombastheniaSandrine Milet-Marsal, Christelle Breillat, Olivier Peyruchaud, et al.
Platelets|March 19, 2002
A novel 196Leu to Pro substitution in the beta3 subunit of the alphaIIbbeta3 integrin in a patient with a variant form of Glanzmann thrombastheniaAlan T Nurden, Jian Ruan, Jean-Max Pasquet, et al.
Thrombosis and Haemostasis|October 7, 2004
Delayed immunologic thrombocytopenia induced by abciximabPaquita Nurden, Gisèle Clofent-Sanchez, Catherine Jais, et al.
Thrombosis and Haemostasis|May 29, 2010
Development of a high-throughput ELISA assay for platelet function testing using platelet-rich plasma or whole bloodIsabelle Salles, Katleen Broos, Alexandre Fontayne, et al.
Plastic and Reconstructive Surgery|February 22, 2007
Reciprocal actions of platelet-secreted TGF-beta1 on the production of VEGF and HGF by human tendon cellsEduardo Anitua, Mikel Sanchez, Alan T Nurden, et al.
Thrombosis and Haemostasis|September 6, 2006
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptideLysiane Hilbert, Paquita Nurden, Claudine Caron, et al.
Haematologica|February 14, 2018
A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of <i>ITGB3</i>: evidence of a dominant effect of gain-of-function mutationsLoredana Bury, Eva Zetterberg, Eva B Leinøe, et al.
Pageof 11