Glanzmann thrombasthenia

Bằng Nurden, Alan T
Được phát hành 2006

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

Bằng Nurden, Alan
Xuất bản năm J Blood Med (2021)

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

Bằng Nurden, Alan T., Nurden, Paquita
Xuất bản năm Haematologica (2018)

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

Bằng Nurden, Paquita, Nurden, Alan T
Xuất bản năm Haematologica (2019)

Inherited thrombocytopenias: history, advances and perspectives

Bằng Nurden, Alan T., Nurden, Paquita
Xuất bản năm Haematologica (2020)

Glanzmann Thrombasthenia: State of the Art and Future Directions

Bằng Nurden, Alan T, Pillois, Xavier, Wilcox, David A.
Được phát hành 2013

Clinical utility gene card for: Glanzmann thrombasthenia

Bằng Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Được phát hành 2012

Clinical utility gene card for: Glanzmann thrombasthenia

Bằng Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Được phát hành 2012

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

Bằng Nurden, Alan, Mercié, Patrick, Zely, Pascal, Nurden, Paquita
Được phát hành 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

Bằng Pillois, Xavier, Peters, Pierre, Segers, Karin, Nurden, Alan T.
Xuất bản năm Mol Genet Genomic Med (2018)

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

Bằng Nurden, Paquita, Stritt, Simon, Favier, Remi, Nurden, Alan T.
Xuất bản năm Haematologica (2020)

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

Bằng Nurden, Paquita, Bordet, Jean-Claude, Pillois, Xavier, Nurden, Alan T.
Xuất bản năm Blood Adv (2017)

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

Bằng Fiore, Mathieu, Pillois, Xavier, Nurden, Paquita, Nurden, Alan T, Austerlitz, Frédéric
Được phát hành 2011

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

Bằng Deppermann, Carsten, Nurden, Paquita, Nurden, Alan T, Nieswandt, Bernhard, Stegner, David
Được phát hành 2013

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

Bằng Hagen, Inger, Nurden, Alan, Bjerrum, Ole Jannik, Solum, Nils Olav, Caen, Jacques
Được phát hành 1980

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

Bằng Nurden, Paquita, Nurden, Alan T, La Marca, Silvia, Punzo, Margherita, Baronciani, Luciano, Federici, Augusto B.
Được phát hành 2009

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

Bằng Laguerre, Michel, Sabi, Essa, Daly, Martina, Stockley, Jacqueline, Nurden, Paquita, Pillois, Xavier, Nurden, Alan T.
Được phát hành 2013

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

Bằng Nurden, Alan T., Nurden, Paquita, Bermejo, Emilsé, Combrié, Robert, McVicar, Daniel W., Washington, A. Valance
Được phát hành 2008

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

Bằng Fang, Juan, Nurden, Paquita, North, Paula, Nurden, Alan T., Du, Lily M., Valentin, Nathalie, Wilcox, David A.
Được phát hành 2013

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

Bằng Saposnik, Béatrice, Binard, Sylvie, Fenneteau, Odile, Nurden, Alan, Nurden, Paquita, Hurtaud-Roux, Marie-Françoise, Schlegel, Nicole
Được phát hành 2014