N. Bernard-Marissal
发表
B. Pettmann,
P. Andersen,
V. Meininger,
2013,
Human mutation.
S. Pradervand,
P. Aebischer,
C. Raoul,
2021,
bioRxiv.
B. Schneider,
R. Chrast,
N. Bernard-Marissal,
2018,
Cell Death & Disease.
R. Chrast,
H. Azzedine,
N. Bernard-Marissal,
2015,
Brain : a journal of neurology.
B. Pettmann,
T. Marissal,
C. Sunyach,
2015,
Neurobiology of Disease.
B. Pettmann,
C. Henderson,
C. Sunyach,
2012,
The Journal of Neuroscience.
O. Poirot,
V. Timmerman,
P. Uhlén,
2019,
Proceedings of the National Academy of Sciences.
G. Lenaers,
P. Reynier,
J. Devaux,
2020
.
M. Bowerman,
R. Kothary,
C. Raoul,
2022,
bioRxiv.
R. Chrast,
H. Azzedine,
N. Bernard-Marissal,
2015
.
A. Mégarbané,
J. Desvignes,
N. Lévy,
2019,
Human molecular genetics.
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.
L. Schöls,
C. Rivolta,
O. Poirot,
2013,
Human molecular genetics.
Rémi Bos,
A. Mégarbané,
F. Brocard,
2021,
Neurobiology of Disease.
S. Pradervand,
P. Aebischer,
C. Raoul,
2022,
Glia.
B. Pettmann,
C. Sunyach,
C. Raoul,
2012,
Neuropharmacology.
B. Pettmann,
C. Raoul,
N. Bernard-Marissal,
2013,
Journal of neurodegenerative diseases.
B. Schneider,
N. Bernard-Marissal,
C. Rochat,
2016
.
C. Verfaillie,
R. Horvath,
D. Pareyson,
2018,
Journal of Neurology, Neurosurgery, and Psychiatry.
R. Chrast,
H. Azzedine,
N. Bernard-Marissal,
2015,
Brain : a journal of neurology.
G. Knott,
J. Auwerx,
P. Aebischer,
2017,
Human molecular genetics.
G. Lenaers,
P. Reynier,
J. Devaux,
2020,
bioRxiv.
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot–Marie–Tooth disease 4H
A. Mégarbané,
J. Borg,
N. Lévy,
2022,
Brain : a journal of neurology.
A. Mégarbané,
J. Borg,
N. Lévy,
2022,
bioRxiv.
B. Schneider,
R. Chrast,
N. Bernard-Marissal,
2018,
Cell Death & Disease.
G. Lenaers,
P. Reynier,
J. Devaux,
2020
.
G. Lenaers,
P. Reynier,
J. Devaux,
2020
.
L. Schöls,
C. Rivolta,
O. Poirot,
2013
.
G. Lenaers,
P. Reynier,
R. Chrast,
2022,
PloS one.
G. Lenaers,
P. Reynier,
R. Chrast,
2020
.