|
🐜
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WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.
19 auth.
K. Balabanian,
B. Lagane,
J. Pablos,
L. Laurent,
T. Planchenault,
O. Vérola,
C. Lebbé,
D. Kérob,
A. Dupuy,
O. Hermine,
...
J. Nicolas,
V. Latger‐Cannard,
D. Bensoussan,
P. Bordigoni,
F. Baleux,
F. Le Deist,
J. Virelizier,
F. Arenzana‐Seisdedos,
F. Bachelerie
|
8 |
2005 |
8
🐜
|
|
🐜
|
Platelet glycoprotein VI binds to polymerized fibrin and promotes thrombin generation.
12 auth.
E. Mammadova-Bach,
V. Ollivier,
S. Loyau,
Mathieu Schaff,
B. Dumont,
R. Favier,
...
G. Freyburger,
V. Latger‐Cannard,
B. Nieswandt,
C. Gachet,
P. Mangin,
M. Jandrot-Perrus
|
7 |
2015 |
7
🐜
|
|
🐜
|
Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis.
11 auth.
P. Mossuz,
F. Girodon,
M. Donnard,
V. Latger‐Cannard,
I. Dobo,
N. Boiret,
...
J. Lecron,
C. Binquet,
C. Barro,
S. Hermouet,
V. Praloran
|
7 |
2004 |
7
🐜
|
|
🐜
|
Spectrum of the Mutations in Bernard–Soulier Syndrome
36 auth.
A. Savoia,
S. Kunishima,
D. De Rocco,
B. Zieger,
M. Rand,
N. Pujol-Moix,
U. Çalişkan,
H. Tokgoz,
A. Pecci,
P. Noris,
A. Srivastava,
C. Ward,
M. Morel-Kopp,
M. Alessi,
S. Bellucci,
...
P. Beurrier,
E. Maistre,
R. Favier,
N. Hézard,
M. Hurtaud-Roux,
V. Latger‐Cannard,
C. Lavenu‐Bombled,
V. Proulle,
S. Meunier,
C. Négrier,
A. Nurden,
H. Randrianaivo,
F. Fabris,
H. Platokouki,
N. Rosenberg,
Basma Hadjkacem,
P. Heller,
M. Karimi,
C. Balduini,
A. Pastore,
F. Lanza
|
7 |
2014 |
7
🐜
|
|
🦁
|
Mean platelet volume: comparison of three analysers towards standardization of platelet morphological phenotype
V. Latger‐Cannard,
M. Hoarau,
S. Salignac,
D. Baumgart,
P. Nurden,
Thomas Lecompte
|
6 |
2012 |
6
🦁
|
|
🐜
|
Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions
11 auth.
M. Beri-Dexheimer,
V. Latger‐Cannard,
C. Philippe,
C. Bonnet,
P. Chambon,
V. Roth,
...
M. Grégoire,
P. Bordigoni,
T. Lecompte,
B. Leheup,
P. Jonveaux
|
6 |
2008 |
6
🐜
|
|
🐜
|
Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia
19 auth.
I. Antony-Debré,
N. Duployez,
M. Bucci,
S. Geffroy,
J. Micol,
Aline Renneville,
N. Boissel,
N. Dhédin,
D. Rea,
B. Nelken,
...
C. Berthon,
T. Leblanc,
M. Mozziconacci,
R. Favier,
P. Heller,
O. Abdel-Wahab,
H. Raslova,
V. Latger‐Cannard,
C. Preudhomme
|
6 |
2016 |
6
🐜
|
|
🦁
|
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders
20 auth.
V. Latger‐Cannard,
C. Philippe,
A. Bouquet,
V. Baccini,
M. Alessi,
A. Ankri,
A. Bauters,
Sophie Bayart,
P. Cornillet-Lefebvre,
S. Daliphard,
...
M. Mozziconacci,
Aline Renneville,
P. Ballerini,
G. Leverger,
H. Sobol,
P. Jonveaux,
C. Preudhomme,
P. Nurden,
T. Lecompte,
R. Favier
|
6 |
2016 |
6
🦁
|
|
🐜
|
How should we diagnose and treat blastic plasmacytoid dendritic cell neoplasm patients?
126 auth.
F. Garnache-Ottou,
C. Vidal,
S. Biichlé,
Florian Renosi,
E. Poret,
Maïder Pagadoy,
M. Desmarets,
A. Roggy,
E. Seillès,
Lou Soret,
F. Schillinger,
S. Puyraimond,
T. Petrella,
C. Preudhomme,
C. Roumier,
...
E. Macintyre,
V. Harrivel,
Y. Desbrosses,
B. Gruson,
F. Geneviève,
S. Thépot,
Yuriy Drebit,
T. Leguay,
F. Gros,
N. Lechevalier,
P. Saussoy,
V. Salaun,
E. Cornet,
Zehaira Benseddik,
R. Veyrat‐Masson,
O. Wagner-Ballon,
C. Salanoubat,
M. Maynadie,
J. Guy,
D. Caillot,
M. Jacob,
J. Cahn,
R. Gressin,
Johan Rose,
B. Quesnel,
E. Guérin,
F. Trimoreau,
J. Feuillard,
M. Gourin,
A. Plesa,
L. Baseggio,
I. Arnoux,
N. Vey,
D. Blaise,
R. Lacroix,
C. Arnoulet,
B. Bénet,
V. Dorvaux,
C. Bret,
B. Drénou,
A. Debliquis,
V. Latger‐Cannard,
C. Bonmati,
M. Béné,
P. Peterlin,
M. Ticchioni,
P. Rohrlich,
A. Arnaud,
S. Wickenhauser,
V. Bardet,
S. Bréchignac,
B. Papoular,
Victoria Raggueneau,
J. Vargaftig,
R. Letestu,
D. Lusina,
T. Braun,
V. Foissaud,
J. Tamburini,
H. Bennani,
N. Freynet,
C. Cordonnier,
M. Le Garff-Tavernier,
N. Jacques,
K. Maloum,
D. Roos-Weil,
D. Bouscary,
V. Asnafi,
L. Lhermitte,
F. Suarez,
E. Lengliné,
F. Féger,
G. Battipaglia,
M. Mohty,
S. Bouyer,
Ouda Ghoual,
Elodie Dindinaud,
Caroline Baslé,
M. Puyade,
C. Lafon,
T. Fest,
M. Roussel,
X. Cahu,
E. Bera,
S. Daliphard,
F. Jardin,
L. Campos,
F. Solly,
D. Guyotat,
A. Galoisy,
A. Eischen,
C. Mayeur‐Rousse,
B. Guffroy,
C. Récher,
M. Loosveld,
A. Garnier,
V. Barlogis,
M. Rosenthal,
S. Brun,
N. Contentin,
S. Maury,
M. Callanan,
C. Lefebvre,
N. Maillard,
P. Okamba,
C. Ferrand,
O. Adotévi,
P. Saas,
Fanny Angelot-Delettre,
Delphine Binda,
E. Deconinck
|
6 |
2019 |
6
🐜
|
|
🐜
|
Human mesenchymal stem cells improve ex vivo expansion of adult human CD34+ peripheral blood progenitor cells and decrease their allostimulatory capacity.
7 auth.
Na Li,
P. Feugier,
B. Serrurrier,
V. Latger‐Cannard,
J. Lesesve,
J. Stoltz,
...
A. Eljaafari
|
6 |
2007 |
6
🐜
|
