V. Decostre
发表
A. Stewart,
G. Piazzesi,
V. Lombardi,
2007,
Cell.
V. Ricotti,
A. Mayhew,
F. Muntoni,
2019,
Neuromuscular Disorders.
L. Servais,
J. Hogrel,
P. Carlier,
2016,
Neurology.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
T. Arimura,
E. Lacène,
M. Malissen,
2012,
Human molecular genetics.
A. Pestronk,
A. Blamire,
J. Mendell,
2019,
Neurology.
A. Pestronk,
A. Blamire,
J. Mendell,
2022
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P. Czernichow,
M. Alison,
J. Hogrel,
2013,
The Journal of clinical endocrinology and metabolism.
R. Carlier,
P. Carlier,
P. Laforêt,
2019,
Muscle & nerve.
L. Servais,
J. Hogrel,
G. Leroux,
2014,
Neuromuscular Disorders.
H. Debaix,
J. Gillis,
V. Decostre,
2002,
Neuromuscular Disorders.
K. Wahbi,
V. Decostre,
F. Pecker,
2012,
Neuromuscular Disorders.
F. Chapon,
G. Bassez,
D. Orlikowski,
2016,
Scientific Reports.
Jean-Yves Hogrel,
Aurélie Canal,
Valérie Doppler,
2015,
BMC Musculoskeletal Disorders.
S. Varnous,
V. Decostre,
F. Pecker,
2018,
Human molecular genetics.
V. Decostre,
G. Bonne,
R. Ben Yaou,
2005,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
J. Gillis,
V. Decostre,
P. Gailly,
2000,
Journal of Muscle Research & Cell Motility.
T. Misteli,
E. Hoffman,
C. Stewart,
2009,
The Journal of cell biology.
V Lombardi,
G Piazzesi,
G. Piazzesi,
2005,
Proceedings of the National Academy of Sciences of the United States of America.
Luc J. Hébert,
Guillaume Bassez,
Bruno Eymard,
2016,
Neuromuscular Disorders.
Paul Pavlidis,
Howard J Worman,
Gisèle Bonne,
2007,
The Journal of clinical investigation.
A. Demoule,
E. Negroni,
C. Coirault,
2014,
Frontiers in Physiology.
Elizabeth Vroom,
Katrijn Klingels,
Laurent Servais,
2013,
Developmental medicine and child neurology.
L. Servais,
F. Leturcq,
P. Sabouraud,
2013,
Neuromuscular Disorders.
F. Metzger,
A. Munnich,
A. Hoeflich,
2012,
PLoS genetics.
E. Mazzone,
A. Mayhew,
E. Mercuri,
2017,
Developmental medicine and child neurology.
Wei Wu,
H. Worman,
A. Schmitt,
2021,
Cell reports.
F. Tesson,
V. Decostre,
G. Bonne,
2012,
PloS one.
Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.
J. Hogrel,
P. Laforêt,
B. Eymard,
2017,
Molecular genetics and metabolism.
Claudia Crocini,
Thomas Eschenhagen,
Arne Hansen,
2013,
Human molecular genetics.
F. Muntoni,
L. Servais,
H. Reyngoudt,
2021,
Annals of clinical and translational neurology.
G. Piazzesi,
V. Lombardi,
M. Reconditi,
2003,
The Journal of physiology.
V. Ricotti,
F. Muntoni,
L. Servais,
2020,
Journal of Neurology.
Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis
Bruno Eymard,
Jean-Yves Hogrel,
Aurélie Canal,
2012,
Neuromuscular Disorders.
J. Hogrel,
P. Laforêt,
B. Eymard,
2016,
Neuromuscular Disorders.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
E. Mazzone,
F. Bianco,
V. Ricotti,
2012,
Neuromuscular Disorders.
J. Hogrel,
C. Alberti,
V. Decostre,
2012,
BMC Musculoskeletal Disorders.
P. Laforêt,
R. Froissart,
V. Decostre,
2023,
European Journal of Medical Research.
L. Servais,
N. Romero,
P. Carlier,
2013,
Neuromuscular Disorders.
T. Misteli,
E. Hoffman,
C. Stewart,
2009,
The Journal of cell biology.
J. Hogrel,
P. Carlier,
B. Matot,
2013,
Neuromuscular Disorders.