|
🐜
|
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2
31 auth.
M. Milh,
N. Boutry‐Kryza,
Julie Sutera-Sardo,
C. Mignot,
S. Auvin,
C. Lacoste,
N. Villeneuve,
A. Roubertie,
B. Héron,
Maryline Carneiro,
A. Kaminska,
C. Altuzarra,
G. Blanchard,
D. Ville,
M. Barthez,
...
D. Heron,
D. Gras,
A. Afenjar,
N. Dorison,
D. Doummar,
T. Billette de Villemeur,
Isabelle An,
A. Jacquette,
P. Charles,
J. Perrier,
B. Isidor,
L. Vercueil,
B. Chabrol,
C. Badens,
G. Lesca,
L. Villard
|
6 |
2013 |
6
🐜
|
|
🦁
|
Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort.
11 auth.
G. Blanchard,
M. Lafforgue,
L. Lion-François,
I. Kemlin,
D. Rodriguez,
P. Castelnau,
...
Maryline Carneiro,
P. Meyer,
F. Rivier,
S. Barbarot,
Y. Chaix
|
6 |
2016 |
6
🦁
|
|
🐜
|
Hashimoto's encephalopathy: identification and long-term outcome in children.
10 auth.
Nafissa Mamoudjy,
C. Korff,
H. Maurey,
G. Blanchard,
Dominique Steshenko,
M. Loiseau-Corvez,
...
B. Husson,
R. Brauner,
M. Tardieu,
K. Deiva
|
5 |
2013 |
5
🐜
|
|
🐜
|
Familial nephrogenic syndrome of inappropriate antidiuresis: dissociation between aquaporin-2 and vasopressin excretion.
11 auth.
B. Ranchin,
Mathieu Boury-Jamot,
G. Blanchard,
L. Dubourg,
A. Hadj‐Aïssa,
D. Morin,
...
T. Durroux,
P. Cochat,
G. Bricca,
J. Verbavatz,
G. Geelen
|
5 |
2010 |
5
🐜
|
|
🐜
|
A proposed diagnostic approach for infantile spasms based on a spectrum of variable aetiology.
8 auth.
A. Poulat,
G. Lesca,
D. Sanlaville,
G. Blanchard,
L. Lion-François,
C. Rougeot,
...
V. des Portes,
D. Ville
|
4 |
2014 |
4
🐜
|
|
🐜
|
A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome
22 auth.
A. Masurel‐Paulet,
A. Piton,
Sophie Chancenotte,
C. Redin,
C. Thauvin-Robinet,
Yvan Henrenger,
D. Minot,
A. Creppy,
Marie Ruffier-Bourdet,
J. Thevenon,
...
P. Kuentz,
D. Lehalle,
A. Curie,
G. Blanchard,
Ezzat Ghosn,
M. Bonnet,
Mélanie Archimbaud-Devilliers,
F. Huet,
Odile Perret,
N. Philip,
J. Mandel,
L. Faivre
|
4 |
2016 |
4
🐜
|
|
🐬
|
Pre- and postnatal imaging of early cerebral damage in Sturge-Weber syndrome
M. Cagneaux,
V. Paoli,
G. Blanchard,
D. Ville,
L. Guibaud
|
3 |
2013 |
3
🐬
|
|
🐜
|
Mosaic 18q21.2 deletions including the TCF4 gene: A clinical report
14 auth.
M. Rossi,
A. Labalme,
M. Cordier,
M. Till,
G. Blanchard,
R. Dubois,
L. Guibaud,
S. Heissat,
E. Javouhey,
A. Lachaux,
...
P. Mure,
D. Ville,
P. Edery,
D. Sanlaville
|
3 |
2012 |
3
🐜
|
