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🐜
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Dehydrated Hereditary Stomatocytosislinked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
18 auth.
J. Albuisson,
Swetha E. Murthy,
M. Bandell,
B. Coste,
Hélène Louis-dit-Picard,
Jayanti Mathur,
Madeleine Fénéant‐Thibault,
G. Tertian,
J. de Jauréguiberry,
Pierre-Yves Syfuss,
...
Stuart M. Cahalan,
L. Garçon,
F. Toutain,
P. Rohrlich,
J. Delaunay,
V. Picard,
X. Jeunemaître,
A. Patapoutian
|
8 |
2013 |
8
🐜
|
|
🐜
|
Correction: Corrigendum: Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
18 auth.
J. Albuisson,
Swetha E. Murthy,
M. Bandell,
B. Coste,
Hélène Louis-dit-Picard,
Jayanti Mathur,
Madeleine Fénéant‐Thibault,
G. Tertian,
J. de Jauréguiberry,
Pierre-Yves Syfuss,
...
Stuart M. Cahalan,
L. Garçon,
F. Toutain,
P. Rohrlich,
J. Delaunay,
V. Picard,
X. Jeunemaître,
A. Patapoutian
|
7 |
2013 |
7
🐜
|
|
🐜
|
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders
9 auth.
M. King,
L. Garçon,
J. Hoyer,
A. Iolascon,
V. Picard,
G. Stewart,
...
P. Bianchi,
S.‐H. Lee,
A. Zanella
|
7 |
2015 |
7
🐜
|
|
🐜
|
A mutation in the Gardos channel is associated with hereditary xerocytosis.
20 auth.
R. Rapetti-Mauss,
C. Lacoste,
V. Picard,
C. Guitton,
E. Lombard,
M. Loosveld,
V. Nivaggioni,
Nathalie Dasilva,
D. Salgado,
J. Desvignes,
...
C. Béroud,
P. Viout,
Monique Bernard,
O. Soriani,
Henri Vinti,
V. Lacroze,
Madeleine Fénéant‐Thibault,
I. Thuret,
H. Guizouarn,
C. Badens
|
6 |
2015 |
6
🐜
|
|
🦁
|
Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients
30 auth.
V. Picard,
C. Guitton,
I. Thuret,
C. Rose,
L. Bendélac,
K. Ghazal,
P. Aguilar-Martinez,
C. Badens,
C. Barro,
C. Bénéteau,
C. Berger,
P. Cathébras,
E. Deconinck,
J. Delaunay,
J. Durand,
...
N. Firah,
F. Galactéros,
B. Godeau,
X. Jaïs,
J. de Jauréguiberry,
C. le Stradic,
F. Lifermann,
Robert Maffre,
G. Morin,
J. Perrin,
V. Proulle,
M. Ruivard,
F. Toutain,
A. Lahary,
L. Garçon
|
6 |
2019 |
6
🦁
|
|
🐢
|
MDR-1 C3435T Polymorphism Influences Cyclosporine A Dose Requirement in Liver-Transplant Recipients
7 auth.
L. Bonhomme‐Faivre,
Aurore Devocelle,
F. Saliba,
Skander Chatled,
J. Maccario,
R. Farinotti,
...
V. Picard
|
6 |
2004 |
6
🐢
|
|
🐜
|
Mutations in promoter region of thrombomodulin and venous thromboembolic disease.
7 auth.
L. Le Flem,
V. Picard,
J. Emmerich,
S. Gandrille,
J. Fiessinger,
M. Aiach,
...
M. Alhenc‐Gelas
|
6 |
1999 |
6
🐜
|
|
🦁
|
Molecular bases of antithrombin deficiency: twenty‐two novel mutations in the antithrombin gene
14 auth.
V. Picard,
U. Nowak-Göttl,
C. Biron-Andréani,
M. Fouassier,
C. Frère,
Michèle Goualt‐Heilman,
E. de Maistre,
S. Régina,
L. Rugeri,
C. Ternisien,
...
Catherine Trichet,
C. Vergnes,
M. Aiach,
M. Alhenc‐Gelas
|
6 |
2006 |
6
🦁
|
|
🦁
|
Antithrombin Phe229Leu: a new homozygous variant leading to spontaneous antithrombin polymerization in vivo associated with severe childhood thrombosis.
V. Picard,
M. Dautzenberg,
B. Villoutreix,
G. Orliaguet,
M. Alhenc‐Gelas,
M. Aiach
|
5 |
2003 |
5
🦁
|
|
🐬
|
Activation-induced exposure of the thrombin anion-binding exosite. Interactions of recombinant mutant prothrombins with thrombomodulin and a thrombin exosite-specific antibody.
Q. Wu,
V. Picard,
M. Aiach,
J. Sadler
|
5 |
1994 |
5
🐬
|
