R. Bernard
发表
Pierre Cau,
Arnold Munnich,
Colin L. Stewart,
2003,
Science.
Nasim Vasli,
Jocelyn Laporte,
Jean Muller,
2012,
Acta Neuropathologica.
M. Didic,
O. Felician,
M. Ceccaldi,
2015,
European Journal of Nuclear Medicine and Molecular Imaging.
N. Lévy,
V. Delague,
R. Bernard,
2007,
NeuroMolecular Medicine.
O. Blin,
J. Hogrel,
J. Pouget,
2009,
The Lancet Neurology.
N. Romero,
N. Lévy,
F. Leturcq,
2006
.
N. Lévy,
J. Vallat,
B. Funalot,
2011,
Neuromuscular Disorders.
N. Philip,
N. Lévy,
P. Latour,
2002,
European Journal of Human Genetics.
G. Chazot,
N. Lévy,
P. Latour,
2001,
Clinical chemistry.
N. Philip,
N. Lévy,
S. Tardieu,
2000,
European Journal of Human Genetics.
N. Philip,
N. Lévy,
J. Bonaventure,
2005,
Clinical genetics.
C. Béroud,
D. Figarella-Branger,
G. Bassez,
2005,
Human mutation.
C. Béroud,
D. Figarella-Branger,
F. Chapon,
2009,
Human mutation.
F. Puppo,
F. Magdinier,
N. Lévy,
2017,
Human mutation.
L. Féasson,
J. Antoine,
A. Casarín,
2012,
Neuromuscular Disorders.
F. Puppo,
F. Magdinier,
M. Bartoli,
2019,
Neurology: Genetics.
M. Claustres,
Jian-Min Chen,
F. Baudat,
2013,
Human mutation.
N. Lévy,
S. Sacconi,
G. Cristofari,
2018,
American journal of medical genetics. Part A.
D. Bozon,
P. Latour,
P. Labauge,
2010,
neurogenetics.
N. Lévy,
V. Delague,
R. Bernard,
2006
.
D. Figarella-Branger,
G. Bassez,
J. Pouget,
2007,
Archives of neurology.
N. Philip,
M. Mattei,
J. Pouget,
2005,
Journal of Medical Genetics.
E. Chouery,
A. Mégarbané,
N. Lévy,
2005,
Genetic counseling.
J. Hassoun,
R. Bernard,
D. Dubois,
1968,
Pathologia Europaea.
C. Béroud,
G. Blandin,
N. Lévy,
2018,
Orphanet Journal of Rare Diseases.
F. Puppo,
F. Magdinier,
N. Lévy,
2014,
Neurology.
S. Julia,
N. Philip,
M. Till,
2015,
Clinical genetics.
Christophe Béroud,
Jamel Chelly,
Mireille Claustres,
2009,
Human mutation.
F. Puppo,
Y. Hayashi,
I. Nishino,
2015,
Human mutation.
F. Puppo,
B. Herberth,
F. Magdinier,
2013,
PLoS genetics.
Shifeng Xue,
F. Magdinier,
B. Wollnik,
2019,
Nucleic acids research.
C. López-Otín,
R. Hennekam,
A. Wagner,
2005,
Human molecular genetics.
R. Hennekam,
A. Verloes,
N. Lévy,
2004,
Human molecular genetics.
A. Mégarbané,
N. Lévy,
J. Vallat,
2003,
Journal of medical genetics.
Hanns Lochmüller,
Thomas Voit,
P K Thomas,
2003,
Human mutation.
F. Magdinier,
J. Pouget,
N. Lévy,
2015,
Orphanet Journal of Rare Diseases.
F. Puppo,
F. Magdinier,
N. Lévy,
2016,
BMC Medical Genetics.
N. Lévy,
A. Béhin,
S. Gorokhova,
2015,
Journal of neuromuscular diseases.
D. Figarella-Branger,
J. Pouget,
N. Lévy,
2003,
Neurology.
N. Lévy,
F. Leturcq,
B. Eymard,
2006,
Clinical genetics.
F. Magdinier,
N. Lévy,
A. Echaniz-Laguna,
2020,
International journal of molecular sciences.
Shifeng Xue,
F. Magdinier,
Christopher,
2019,
Nucleic acids research.
J. Pouget,
N. Lévy,
A. Bensimon,
2011,
Annals of neurology.
C. Béroud,
F. Chapon,
V. Drouin‐Garraud,
2007,
Clinical genetics.
Albert David,
Jon Andoni Urtizberea,
Bruno Eymard,
2019,
Journal of Medical Genetics.
N. Lévy,
W. G. Voogt,
M. Krahn,
2013,
European journal of neurology.
F. Magdinier,
S. Attarian,
E. Novoa-Del-Toro,
2021,
Journal of cachexia, sarcopenia and muscle.
F. Rivier,
C. Béroud,
F. Chapon,
2022,
Orphanet Journal of Rare Diseases.
F. Puppo,
I. Nishino,
M. Bartoli,
2014,
Neuromuscular Disorders.
M. Barat‐Houari,
F. Vasseur,
J. Pouget,
2010,
European Journal of Human Genetics.
J. Hassoun,
R. Bernard,
J. Pellissier,
2004,
Acta Neuropathologica.
N. Lévy,
V. Delague,
R. Bernard,
2013,
Annals of Human Genetics.
N. Lévy,
O. Dubourg,
P. Laforêt,
2008,
Revue neurologique.
F. Puppo,
Y. Hayashi,
I. Nishino,
2015
.
P. Perrin,
F. Magdinier,
R. Bernard,
2023,
Neurology: Genetics.