Suchergebnisse - "Nurden, Paquita"

PubPharm (23)

1

Correction of Severe Myelofibrosis, Impaired Platelet Functions and Abnormalities in a Patient with Gray Platelet Syndrome Successfully Treated by Stem Cell Transplantation

enthalten in: Platelets | 2020

von Favier, R. | Roussel, X. | Audia, S. | +10

2

A Glanzmann thrombasthenia family associated with a TUBB1-related macrothrombocytopenia

enthalten in: Journal of thrombosis and haemostasis : JTH | 2019

von Guillet, B. | Bayart, S. | Pillois, X. | +3

3

A novel missense mutation in a leucine-rich repeat of GPIbα in a Bernard-Soulier variant reduces shear-dependent adherence on von Willebrand factor

enthalten in: British journal of haematology | 2019

von Proulle, V. | Strassel, C. | Perrault, C. | +10

4

Management of pregnancy for a patient with the new syndromic macrothrombocytopenia, DIAPH1-related disease

enthalten in: Platelets | 2018

von Nurden, P. | Nurden, A. | Favier, R. | +1

5

Marked bleeding diathesis in patients with platelet dysfunction due to a novel mutation in RASGRP2, encoding CalDAG-GEFI (p.Gly305Asp)

enthalten in: Platelets | 2018

von Bermejo, E. | Alberto, M. | Paul, D. | +5

6

Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin αIIbβ3 Activation

enthalten in: Arteriosclerosis, thrombosis, and vascular biology | 2017

von Berrou, E. | Adam, F. | Lebret, M. | +11

7

Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect

enthalten in: Nature communications | 2014

von Bender, M. | Stritt, S. | Nurden, P. | +15

ErratumIn: Nat Commun. 2015;6:6507 Heinze, Katrin [corrected to Heinze, Katrin G]. - PMID 25744693

8

Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome

enthalten in: Blood | 2011

von Nurden, P. | Debili, N. | Coupry, I. | +17

9

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

10

A unique combination of inhibitory and partially activating mutations in beta3 of a patient with variant-type Glanzmann thrombasthenia

enthalten in: Platelets | 2010

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