C. Cances
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J. Albucher,
C. Cognard,
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Pediatric neurology.
G. Comi,
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N. Goemans,
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Orphanet Journal of Rare Diseases.
M. Koenig,
N. Romero,
M. Cossée,
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Journal of Medical Genetics.
A. Afenjar,
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D. Ville,
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Epilepsia.
M. Baulac,
P. Striano,
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L. Servais,
J. Hogrel,
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Annals of clinical and translational neurology.
F. Rivier,
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Neurology.
N. Boddaert,
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Epilepsia.
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N. Boddaert,
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European journal of medical genetics.
F. Rivier,
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Neuropediatrics.
N. Romero,
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European journal of neurology.
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Orphanet Journal of Rare Diseases.
L. Servais,
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Neurology.
S. Quijano-roy,
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Neurology.
L. Servais,
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Journal of neuromuscular diseases.
F. Rivier,
M. Cossée,
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European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
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N. Romero,
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Annals of neurology.
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Nature Genetics.
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Nature Genetics.
J. J. Padilla,
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Neuromuscular Disorders.
F. Rivier,
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P. Sabouraud,
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International journal of molecular sciences.
H. Cavé,
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American journal of medical genetics. Part A.
S. Julia,
J. Plaisancié,
A. Vigouroux,
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European journal of medical genetics.
L. Cif,
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Journal of the Neurological Sciences.
F. Rivier,
F. Chapon,
C. Richelme,
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Orphanet Journal of Rare Diseases.
M. Jaatun,
K. Katanyuwong,
P. Kwan,
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Epilepsia open.
S. Auvin,
M. Schaeffer,
R. Nabbout,
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Epilepsy Research.
S. Auvin,
B. Dozières-Puyravel,
Louis Dufour,
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Epilepsy & Behavior.
M. Jaatun,
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E. Pataraia,
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Orphanet Journal of Rare Diseases.
C. Cancés,
M. Mejdoubi,
M. Tauber,
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Child's Nervous System.
Y. Chaix,
C. Cances,
R. Honorat,
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Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
F. Rivier,
E. Uro-Coste,
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Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
D. Zélénika,
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Nature Genetics.
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European journal of medical genetics.
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N. Romero,
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N. Boddaert,
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Epilepsia.
L. Servais,
J. Hogrel,
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PloS one.
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Neuromuscular Disorders.
M. Tauber,
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C. Guilbeau-Frugier,
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Hormone Research in Paediatrics.
M. Teichmann,
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Neurology: Genetics.
E. Cheuret,
C. Bréhin,
J. Rittié,
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Archives de pédiatrie.
C. Cancés,
E. Bieth,
M. Longy,
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European journal of medical genetics.
F. Rivier,
P. Cintas,
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Neuropediatrics.
L. Vallée,
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J. Cuisset,
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Muscle & nerve.
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Neuropediatrics.
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Archives of neurology.
S. Lehmann,
M. Koenig,
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P. Derambure,
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Epilepsia.
ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate
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Epilepsia.
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C. Hachon Le Camus,
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The New England journal of medicine.
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G. Lenaers,
N. Leboucq,
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European journal of neurology.
M. Koenig,
F. Rivier,
M. Cossée,
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The Journal of molecular diagnostics : JMD.
Y. Péréon,
P. Cintas,
C. Barnérias,
2023,
Neuromuscular Disorders.
D. Vissière,
L. Servais,
Y. Péréon,
2017,
Neuromuscular Disorders.
M. Jaatun,
K. Katanyuwong,
E. Pataraia,
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Orphanet Journal of Rare Diseases.
F. Rivier,
U. Walther-Louvier,
É. Baudou,
2018,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
R. Nabbout,
D. Ville,
J. Pedespan,
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Frontiers in Neurology.
D. Zélénika,
P. Nitschké,
D. Lacombe,
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Nature Genetics.
M. Mayer,
B. Estournet,
P. Sabouraud,
2014,
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
F. Rivier,
P. Sabouraud,
C. Barnérias,
2020,
Frontiers in Pediatrics.
C. Richelme,
C. Barnérias,
C. Espil,
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Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
G. Touati,
T. Levade,
F. Sabourdy,
2019,
International journal of molecular sciences.
R. Finkel,
M. Pane,
A. Mayhew,
2023,
Neurology and Therapy.
F. Giuliano,
P. Cintas,
S. Quijano-roy,
2019,
Neuromuscular Disorders.
P. Latour,
T. Levade,
A. Brassier,
2017,
Orphanet Journal of Rare Diseases.
N. Garcelon,
R. Nabbout,
A. Kaminska,
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Genetics in Medicine.
M. Koenig,
F. Rivier,
M. Cossée,
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O. Blin,
L. Vallée,
P. Franco,
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Annals of clinical and translational neurology.
M. Cossée,
F. Leturcq,
Y. Péréon,
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Journal of Neurology.
C. Dimeglio,
É. Baudou,
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2019,
BMC Pediatrics.
A. Afenjar,
N. Philip,
D. Ville,
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Epilepsia.
D. Zélénika,
P. Nitschké,
D. Lacombe,
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N. Boddaert,
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Epilepsia.
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M. Pane,
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Neuromuscular Disorders.
B. Echenne,
C. Richelme,
M. Picot,
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Revue neurologique.