A unique combination of inhibitory and partially activating mutations in &bgr;3 of a patient with variant-type Glanzmann thrombasthenia

By Nurden Alan T.   Fernandes Helder   Fiore Mathieu   Nurden Paquita   Vinciguerra Christine   Martins Nathalie   Sirvain-Trukniewicz Peggy   Couloux Arnaud   Heilig Roland   Pillois Xavier  

Platelets, Vol. 21, Iss. 6, 2010-09 ,pp. : 498-500

Informa Healthcare

Access to resources Recommend Favorite

Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India

By Vijapurkar Manasi   Ghosh Kanjaksha   Shetty Shrimati  

Platelets, Vol. 20, Iss. 1, 2009-02 ,pp. : 35-40

Informa Healthcare

Access to resources Recommend Favorite

αIIbG236E causes Glanzmann thrombasthenia by impairing association with β3

By Afrasiabi A.   Gelain F.   Artoni A.   Mannucci P. M.  

Platelets, Vol. 19, Iss. 5, 2008-08 ,pp. : 322-327

Informa Healthcare

Access to resources Recommend Favorite

Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations??

By Nurden Alan T.   Fiore Mathieu   Nurden Paquita   Heilig Roland   Pillois Xavier  

Platelets, Vol. 22, Iss. 7, 2011-11 ,pp. : 547-551

Informa Healthcare

Access to resources Recommend Favorite

A novel ¹⁹⁶Leu to Pro substitution in the β3 subunit of the αIIbβ3 integrin in a patient with a variant form of Glanzmann thrombasthenia

By Nurden Alan T.   Ruan Jian   Pasquet Jean-Max   Gauthier Bruno   Combrié Robert   Kunicki Thomas   Nurden Paquita  

Platelets, Vol. 13, Iss. 2, 2002-03 ,pp. : 101-111

Informa Healthcare

Access to resources Recommend Favorite