Suchergebnisse - "Nurden, Paquita"

PubPharm (211)

101

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

enthalten in: Thrombosis and haemostasis | 2011

von Bartsch, I. | Sandrock, K. | Lanza, F. | +12

102

Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

enthalten in: Nature genetics | 2011

von Albers, C. | Cvejic, A. | Favier, R. | +17

103

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

enthalten in: Platelets | 2011

von Nurden, A. | Fiore, M. | Nurden, P. | +2

104

Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

enthalten in: Nature genetics | 2011

von Albers, C. | Cvejic, A. | Favier, R. | +17

105

Megakaryocytes possess a functional intrinsic apoptosis pathway that must be restrained to survive and produce platelets

enthalten in: The journal of cell biology | 2011

von Josefsson, E. | James, C. | Henley, K. | +14

106

Megakaryocytes possess a functional intrinsic apoptosis pathway that must be restrained to survive and produce platelets

enthalten in: The journal of experimental medicine | 2011

von Josefsson, E. | James, C. | Henley, K. | +14

107

Antagonism of P2Y12 reduces physiological thromboxane levels

enthalten in: Platelets | 2010

von Bhavaraju, K. | Georgakis, A. | Jin, J. | +5

108

Le CD154 plaquettaire : Une nouvelle interface dans l’hémostase et la réaction inflammatoire

enthalten in: Médecine sciences | 2010

von Delmas, Y. | Viallard, J. | Villeneuve, J. | +9

109

Rapid diagnosis of the French gypsy mutation in Glanzmann thrombasthenia using high-resolution melting analysis

enthalten in: Thrombosis and haemostasis | 2010

von Fiore, M. | Nurden, A. | Vinciguerra, C. | +2

110

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

enthalten in: Platelets | 2010

von Nurden, A. | Fernandes, H. | Fiore, M. | +7