|
🐜
|
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
79 auth.
Ilenia Simeoni,
J. Stephens,
Fengyuan Hu,
Sri V. V. Deevi,
K. Megy,
T. Bariana,
C. Lentaigne,
Sol Schulman,
S. Sivapalaratnam,
Minka J. A. Vries,
S. Westbury,
D. Greene,
S. Papadia,
M. Alessi,
A. Attwood,
...
M. Ballmaier,
G. Baynam,
E. Bermejo,
M. Bertoli,
P. Bray,
L. Bury,
M. Cattaneo,
P. Collins,
L. Daugherty,
R. Favier,
D. French,
B. Furie,
M. Gattens,
M. Germeshausen,
C. Ghevaert,
A. Goodeve,
J. Guerrero,
D. Hampshire,
D. Hart,
J. Heemskerk,
Y. Henskens,
M. Hill,
Nancy Hogg,
J. Jolley,
W. Kahr,
A. Kelly,
R. Kerr,
Myrto A. Kostadima,
S. Kunishima,
Michele P. Lambert,
R. Liesner,
José A López,
R. Mapeta,
M. Mathias,
C. Millar,
A. Nathwani,
M. Neerman-Arbez,
A. Nurden,
P. Nurden,
M. Othman,
K. Peerlinck,
D. Perry,
Pawan Poudel,
P. Reitsma,
M. Rondina,
P. Smethurst,
W. Stevenson,
A. Szkotak,
Salih Tuna,
C. van Geet,
Deborah Whitehorn,
D. Wilcox,
Bin Zhang,
S. Revel-Vilk,
P. Gresele,
D. Bellissimo,
C. Penkett,
M. Laffan,
A. Mumford,
A. Rendon,
K. Gomez,
K. Freson,
W. Ouwehand,
E. Turro
|
7 |
2016 |
7
🐜
|
|
🦁
|
Effect of nitroxyl on human platelets function
E. Bermejo,
D. Sáenz,
F. Alberto,
R. Rosenstein,
S. Bari,
M. Lazzari
|
5 |
2005 |
5
🦁
|
|
🐜
|
Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding.
21 auth.
S. Westbury,
M. Canault,
D. Greene,
E. Bermejo,
K. Hanlon,
Michele P. Lambert,
C. Millar,
P. Nurden,
S. Obaji,
S. Revel-Vilk,
...
C. van Geet,
K. Downes,
S. Papadia,
Salih Tuna,
C. Watt,
K. Freson,
M. Laffan,
W. Ouwehand,
M. Alessi,
E. Turro,
A. Mumford
|
5 |
2017 |
5
🐜
|
|
🐜
|
Protective role of nitric oxide in mice with Shiga toxin-induced hemolytic uremic syndrome.
8 auth.
G. Dran,
G. Fernández,
C. Rubel,
E. Bermejo,
S. Gómez,
R. Meiss,
...
M. Isturiz,
M. Palermo
|
5 |
2002 |
5
🐜
|
|
🐜
|
Delayed immunologic thrombocytopenia induced by abciximab
7 auth.
P. Nurden,
G. Clofent-Sanchez,
C. Jais,
E. Bermejo,
L. Leroux,
P. Coste,
...
A. Nurden
|
4 |
2004 |
4
🐜
|
|
🦁
|
Marked bleeding diathesis in patients with platelet dysfunction due to a novel mutation in RASGRP2, encoding CalDAG-GEFI (p.Gly305Asp)
8 auth.
E. Bermejo,
M. Alberto,
David S. Paul,
Aaron A. Cook,
P. Nurden,
A. Sánchez Luceros,
...
A. Nurden,
W. Bergmeier
|
4 |
2018 |
4
🦁
|
|
🐜
|
Identification of p.W246L As a Novel Mutation in the GP1BA Gene Responsible for Platelet-Type von Willebrand Disease
8 auth.
A. Woods,
A. Sánchez-Luceros,
E. Bermejo,
Juvenal Paiva,
M. Alberto,
S. Grosso,
...
A. Kempfer,
M. Lazzari
|
4 |
2014 |
4
🐜
|
|
🐬
|
Phenotypic heterogeneity in the gray platelet syndrome extends to the expression of TREM family member, TLT-1
A. Nurden,
P. Nurden,
E. Bermejo,
R. Combrié,
D. McVicar,
A. Washington
|
4 |
2008 |
4
🐬
|
