Glanzmann thrombasthenia

по Nurden, Alan T
Опубликовано 2006

Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?

по Nurden, Alan
Опубликовано в: J Blood Med (2021)

High-throughput sequencing for rapid diagnosis of inherited platelet disorders: a case for a European consensus

по Nurden, Alan T., Nurden, Paquita
Опубликовано в: Haematologica (2018)

Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?

по Nurden, Paquita, Nurden, Alan T
Опубликовано в: Haematologica (2019)

Inherited thrombocytopenias: history, advances and perspectives

по Nurden, Alan T., Nurden, Paquita
Опубликовано в: Haematologica (2020)

Glanzmann Thrombasthenia: State of the Art and Future Directions

по Nurden, Alan T, Pillois, Xavier, Wilcox, David A.
Опубликовано 2013

Clinical utility gene card for: Glanzmann thrombasthenia

по Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Опубликовано 2012

Clinical utility gene card for: Glanzmann thrombasthenia

по Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Опубликовано 2012

Deep Vein Thrombosis, Raynaud's Phenomenon, and Prinzmetal Angina in a Patient with Glanzmann Thrombasthenia

по Nurden, Alan, Mercié, Patrick, Zely, Pascal, Nurden, Paquita
Опубликовано 2012

In silico analysis of structural modifications in and around the integrin αIIb genu caused by ITGA2B variants in human platelets with emphasis on Glanzmann thrombasthenia

по Pillois, Xavier, Peters, Pierre, Segers, Karin, Nurden, Alan T.
Опубликовано в: Mol Genet Genomic Med (2018)

Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy

по Nurden, Paquita, Stritt, Simon, Favier, Remi, Nurden, Alan T.
Опубликовано в: Haematologica (2020)

An intracytoplasmic β3 Leu718 deletion in a patient with a novel platelet phenotype

по Nurden, Paquita, Bordet, Jean-Claude, Pillois, Xavier, Nurden, Alan T.
Опубликовано в: Blood Adv (2017)

Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families

по Fiore, Mathieu, Pillois, Xavier, Nurden, Paquita, Nurden, Alan T, Austerlitz, Frédéric
Опубликовано 2011

The Nbeal2(−/−) mouse as a model for the gray platelet syndrome

по Deppermann, Carsten, Nurden, Paquita, Nurden, Alan T, Nieswandt, Bernhard, Stegner, David
Опубликовано 2013

Immunochemical Evidence for Protein Abnormalities in Platelets from Patients with Glanzmann's Thrombasthenia and Bernard-Soulier Syndrome

по Hagen, Inger, Nurden, Alan, Bjerrum, Ole Jannik, Solum, Nils Olav, Caen, Jacques
Опубликовано 1980

Platelet morphological changes in 2 patients with von Willebrand disease type 3 caused by large homozygous deletions of the von Willebrand factor gene

по Nurden, Paquita, Nurden, Alan T, La Marca, Silvia, Punzo, Margherita, Baronciani, Luciano, Federici, Augusto B.
Опубликовано 2009

Molecular Dynamics Analysis of a Novel β3 Pro189Ser Mutation in a Patient with Glanzmann Thrombasthenia Differentially Affecting αIIbβ3 and αvβ3 Expression

по Laguerre, Michel, Sabi, Essa, Daly, Martina, Stockley, Jacqueline, Nurden, Paquita, Pillois, Xavier, Nurden, Alan T.
Опубликовано 2013

Phenotypic Heterogeneity in the Gray Platelet Syndrome Extends to the Expression of TREM Family Member, TLT-1

по Nurden, Alan T., Nurden, Paquita, Bermejo, Emilsé, Combrié, Robert, McVicar, Daniel W., Washington, A. Valance
Опубликовано 2008

C560Rβ3 caused platelet integrin αIIbβ3 to Bind Fibrinogen Continuously yet Resulted in a Severe Bleeding Syndrome and Increased Murine Mortality

по Fang, Juan, Nurden, Paquita, North, Paula, Nurden, Alan T., Du, Lily M., Valentin, Nathalie, Wilcox, David A.
Опубликовано 2013

Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders

по Saposnik, Béatrice, Binard, Sylvie, Fenneteau, Odile, Nurden, Alan, Nurden, Paquita, Hurtaud-Roux, Marie-Françoise, Schlegel, Nicole
Опубликовано 2014