M. Mayer
发表
L. Servais,
I. Nelson,
N. Romero,
2016,
American journal of human genetics.
F. Rivier,
F. Chapon,
C. Richelme,
2019,
Orphanet Journal of Rare Diseases.
T. Billette de Villemeur,
B. Héron,
K. Maincent,
2018,
Orphanet Journal of Rare Diseases.
O. Dulac,
C. Chiron,
R. Nabbout,
2006,
Epilepsia.
R. Carlier,
L. Viollet,
B. Estournet,
2006,
Brain and Development.
Alice Barateau,
C. Vigouroux,
B. Buendia,
2017,
PloS one.
L. Servais,
J. Dowling,
A. D’Amico,
2019,
Neurology.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
F. Leturcq,
J. Chelly,
C. Chiron,
2009,
PloS one.
Kiely N. James,
D. Horn,
T. Wieland,
2018,
Human Genetics.
Arturo E. Hernandez,
B. Carlin,
E. Bertini,
2021,
Orphanet Journal of Rare Diseases.
I. Desguerre,
T. Arimura,
H. Worman,
2004,
Muscle & nerve.
M. Ruberg,
A. Brice,
N. Birouk,
2007,
NeuroMolecular Medicine.
A. Afenjar,
D. Rodriguez,
T. Billette de Villemeur,
2020,
Neurology: Genetics.
A. Sureau,
J. Rendu,
B. Eymard,
2020,
Neurology: Genetics.
F. Muntoni,
I. Desguerre,
H. Topaloglu,
1998,
American journal of human genetics.
K. Flanigan,
J. Dowling,
B. Ilkovski,
2010,
Neuromuscular Disorders.
F. Rivier,
C. Richelme,
G. Bassez,
2019,
Neurology.
E. Mercuri,
F. Muntoni,
T. Pierson,
2021,
Brain communications.
E. Bertini,
B. Schlotter-Weigel,
E. Malfatti,
2020,
Neurology.
E. Mercuri,
F. Muntoni,
F. Rivier,
2017,
The Lancet Neurology.
P. Amati‐Bonneau,
P. Reynier,
D. Rodriguez,
2012,
Brain : a journal of neurology.
F. Rivier,
A. Toutain,
B. Echenne,
2009,
Human molecular genetics.
C. Garel,
A. Toutain,
D. Rodriguez,
2016,
Clinical genetics.
Myostatin: a Circulating Biomarker Correlating with Disease in Myotubular Myopathy Mice and Patients
Arturo E. Hernandez,
L. Servais,
A. D’Amico,
2020,
Molecular therapy. Methods & clinical development.
R. Porcher,
D. Annane,
P. Ravaud,
2021,
European heart journal.
N. Romero,
E. Uro-Coste,
J. Bevilacqua,
2007,
Annals of neurology.
K. Campbell,
N. Romero,
F. Leturcq,
1997,
Neurology.
M. Cossée,
M. Claustres,
F. Leturcq,
2016,
Journal of neuromuscular diseases.
Lennart Opitz,
Peter Nürnberg,
Johannes Schumacher,
2009,
Nature Genetics.
F. Rivier,
A. Toutain,
B. Echenne,
2010,
Annals of neurology.
M. Ruberg,
A. Brice,
N. Lévy,
1998,
Human molecular genetics.
P. Laforêt,
B. Eymard,
L. Chatenoud,
2008,
Neuromuscular Disorders.
C. Béroud,
F. Leturcq,
J. Kaplan,
2004,
Neuromuscular Disorders.
M. Hanna,
B. Fontaine,
S. Vicart,
2008,
Neurology.
H. Lochmüller,
M. Mayer,
B. Maturi,
2021,
Journal of neuromuscular diseases.
A. Afenjar,
N. Dorison,
J. Le Gargasson,
2012,
European journal of medical genetics.
E. Génin,
H. Lochmüller,
J. Pouget,
2008,
Neurology.
E. Génin,
J. Pouget,
A. Barois,
2008
.
E. Bertini,
S. Naidu,
D. Rodriguez,
2005,
Neurology.
E. Bertini,
K. Pelin,
E. Mercuri,
2014,
Human mutation.
R. Porcher,
É. Marijon,
A. Lazarus,
2019,
Circulation.
A. Barois,
B. Eymard,
B. Hainque,
2003,
Journal of medical genetics.
A. Brice,
V. Drouin‐Garraud,
C. Thauvin,
2014,
Orphanet Journal of Rare Diseases.
C Adamsbaum,
C. Adamsbaum,
G. Kalifa,
1992,
Neurology.
F. Lofaso,
B. Fauroux,
K. Maincent,
2011,
European Respiratory Journal.
A. Bigot,
K. Mamchaoui,
S. Quijano-roy,
2014,
Journal of Cell Science.
M. Momtchilova,
D. Heron,
C. Mignot,
2013,
Brain and Development.
F. Rivier,
P. Sabouraud,
C. Barnérias,
2020,
Frontiers in Pediatrics.
F. Gottrand,
J. Salleron,
V. Tiffreau,
2011,
British Journal of Nutrition.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
A. Munnich,
D. Bonneau,
L. Viollet,
2004,
European Journal of Human Genetics.
V. Dubowitz,
B. Estournet,
D. Hillaire,
1994,
Human molecular genetics.
T. Voit,
L. Servais,
S. Quijano-roy,
2013,
Neuromuscular Disorders.
F. Gottrand,
J. Salleron,
V. Tiffreau,
2011,
British Journal of Nutrition.