Glanzmann thrombasthenia

Por Nurden, Alan T
Publicado em 2006

Glanzmann Thrombasthenia: State of the Art and Future Directions

Por Nurden, Alan T, Pillois, Xavier, Wilcox, David A.
Publicado em 2013

Clinical utility gene card for: Glanzmann thrombasthenia

Por Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Publicado em 2012

Clinical utility gene card for: Glanzmann thrombasthenia

Por Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri
Publicado em 2012

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

Por Nurden, Alan, Mercié, Patrick, Zely, Pascal, Nurden, Paquita
Publicado em 2012

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

Por Fiore, Mathieu, Pillois, Xavier, Nurden, Paquita, Nurden, Alan T, Austerlitz, Frédéric
Publicado em 2011

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

Por Deppermann, Carsten, Nurden, Paquita, Nurden, Alan T, Nieswandt, Bernhard, Stegner, David
Publicado em 2013

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

Por Hagen, Inger, Nurden, Alan, Bjerrum, Ole Jannik, Solum, Nils Olav, Caen, Jacques
Publicado em 1980

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

Por Nurden, Paquita, Nurden, Alan T, La Marca, Silvia, Punzo, Margherita, Baronciani, Luciano, Federici, Augusto B.
Publicado em 2009

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

Por Laguerre, Michel, Sabi, Essa, Daly, Martina, Stockley, Jacqueline, Nurden, Paquita, Pillois, Xavier, Nurden, Alan T.
Publicado em 2013

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

Por Nurden, Alan T., Nurden, Paquita, Bermejo, Emilsé, Combrié, Robert, McVicar, Daniel W., Washington, A. Valance
Publicado em 2008

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

Por Fang, Juan, Nurden, Paquita, North, Paula, Nurden, Alan T., Du, Lily M., Valentin, Nathalie, Wilcox, David A.
Publicado em 2013

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

Por Saposnik, Béatrice, Binard, Sylvie, Fenneteau, Odile, Nurden, Alan, Nurden, Paquita, Hurtaud-Roux, Marie-Françoise, Schlegel, Nicole
Publicado em 2014

A prototypic platelet septin and its participation in secretion

Por Dent, Judith, Kato, Kazunobu, Peng, Xiao-Rong, Martinez, Constantino, Cattaneo, Marco, Poujol, Christel, Nurden, Paquita, Nurden, Alan, Trimble, William S., Ware, Jerry
Publicado em 2002

Gray platelet syndrome and defective thrombo-inflammation in Nbeal2-deficient mice

Por Deppermann, Carsten, Cherpokova, Deya, Nurden, Paquita, Schulz, Jan-Niklas, Thielmann, Ina, Kraft, Peter, Vögtle, Timo, Kleinschnitz, Christoph, Dütting, Sebastian, Krohne, Georg, Eming, Sabine A., Nurden, Alan T., Eckes, Beate, Stoll, Guido, Stegner, David, Nieswandt, Bernhard
Publicado em 2013

Procoagulant Platelets Form an α-Granule Protein-covered “Cap” on Their Surface That Promotes Their Attachment to Aggregates

Por Abaeva, Anastasia A., Canault, Matthias, Kotova, Yana N., Obydennyy, Sergey I., Yakimenko, Alena O., Podoplelova, Nadezhda A., Kolyadko, Vladimir N., Chambost, Herve, Mazurov, Aleksei V., Ataullakhanov, Fazoil I., Nurden, Alan T., Alessi, Marie-Christine, Panteleev, Mikhail A.
Publicado em 2013

Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A

Por Du, Lily M., Nurden, Paquita, Nurden, Alan T., Nichols, Timothy C., Bellinger, Dwight A., Jensen, Eric S., Haberichter, Sandra L., Merricks, Elizabeth, Raymer, Robin A., Fang, Juan, Koukouritaki, Sevasti B., Jacobi, Paula M., Hawkins, Troy B., Cornetta, Kenneth, Shi, Qizhen, Wilcox, David A.
Publicado em 2013

Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding

Por Canault, Matthias, Ghalloussi, Dorsaf, Grosdidier, Charlotte, Guinier, Marie, Perret, Claire, Chelghoum, Nadjim, Germain, Marine, Raslova, Hana, Peiretti, Franck, Morange, Pierre E., Saut, Noemie, Pillois, Xavier, Nurden, Alan T., Cambien, François, Pierres, Anne, van den Berg, Timo K., Kuijpers, Taco W., Alessi, Marie-Christine, Tregouet, David-Alexandre
Publicado em 2014

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

Por Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Publicado em 2011

Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg(2+) homeostasis and cytoskeletal architecture

Por Stritt, Simon, Nurden, Paquita, Favier, Remi, Favier, Marie, Ferioli, Silvia, Gotru, Sanjeev K., van Eeuwijk, Judith M M., Schulze, Harald, Nurden, Alan T., Lambert, Michele P., Turro, Ernest, Burger-Stritt, Stephanie, Matsushita, Masayuki, Mittermeier, Lorenz, Ballerini, Paola, Zierler, Susanna, Laffan, Michael A., Chubanov, Vladimir, Gudermann, Thomas, Nieswandt, Bernhard, Braun, Attila
Publicado no Nat Commun (2016)