R. Juntas-Morales
发表
L. Kremer,
T. Maisonobe,
A. Echaniz-Laguna,
2020,
Journal of Neurology.
L. Kremer,
David John Adams,
T. Maisonobe,
2020,
Clinical Neurophysiology.
Victor R. Martinez,
C. Blackstone,
M. Stamelou,
2021,
Movement disorders : official journal of the Movement Disorder Society.
A. Al-Chalabi,
C. Garlanda,
P. Leigh,
2020,
EBioMedicine.
A. Al-Chalabi,
P. Leigh,
U. Andréasson,
2020
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M. Codina-Solà,
E. García-Arumí,
J. Sotoca,
2022,
Genes.
F. Rivier,
P. Latour,
P. Cintas,
2022,
Neuropediatrics.
N. Lévy,
A. Echaniz-Laguna,
Y. Péréon,
2021,
European journal of neurology.
J. Daurès,
C. Raoul,
W. Camu,
2014,
Neurobiology of Aging.
J. Díaz-Manera,
C. Domínguez-González,
A. Rivera-Gallego,
2022,
Orphanet Journal of Rare Diseases.
M. Druet‐Cabanac,
P. Preux,
F. Paraf,
2014,
BMJ Open.
P. Vidalain,
C. Delaugerre,
P. Roingeard,
2019,
Nature.
J. Sotoca,
M. Salvadó,
D. Sánchez-Tejerina,
2022,
Journal of clinical medicine.
S. Coppens,
E. Pierce-Hoffman,
L. Servais,
2019,
Annals of neurology.
M. Codina-Solà,
E. García-Arumí,
E. Martínez-Sáez,
2023,
Neuromuscular Disorders.
M. Codina-Solà,
E. García-Arumí,
E. Martínez-Sáez,
2022,
Clinical genetics.
M. Penas-Prado,
J. Díaz-Guzmán,
R. Juntas-Morales,
2001,
Revista de neurología (Ed. impresa).
W. Camu,
R. Juntas-Moralès,
N. Pageot,
2016,
European Neurology.
J. Sotoca,
A. Palasí,
M. Salvadó,
2023,
Acta Neurologica Scandinavica.
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
P. Latour,
T. Stojkovic,
C. Goizet,
2019,
European Journal of Human Genetics.
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
P. Latour,
T. Stojkovic,
C. Goizet,
2019,
European Journal of Human Genetics.
Sachit Shah,
J. Polke,
M. Reilly,
2021,
Journal of Neurology, Neurosurgery, and Psychiatry.
N. Glaichenhaus,
G. Siciliano,
S. Sacconi,
2021,
Journal of neuromuscular diseases.
A. Al-Chalabi,
P. Leigh,
C. Garlanda,
2021,
Brain communications.
J. Sotoca,
M. Salvadó,
D. Sánchez-Tejerina,
2023,
Cells.
Adam L. Comer,
Robert G. Miller,
S. Demeret,
2023,
The Lancet Neurology.
C. Raoul,
P. Corcia,
P. Couratier,
2017,
Molecular Neurobiology.
Annelot M. Dekker,
A. Destée,
S. Bates,
2017,
The Lancet Neurology.
S. Lehmann,
E. Thouvenot,
W. Camu,
2020,
European journal of neurology.
M. Picot,
W. Camu,
S. Lumbroso,
2020,
Frontiers in Neuroscience.
M. Picot,
W. Camu,
A. Dupuy,
2020,
Frontiers in Neurology.
F. Sedel,
W. Camu,
R. Juntas-Moralès,
2020,
EClinicalMedicine.
J. Glass,
T. Ferguson,
M. Bromberg,
2018,
Clinical Neurophysiology.
W. Camu,
F. Esselin,
G. Taieb,
2021,
Journal of Neuroscience and Neurological Disorders.
M. Codina-Solà,
E. García-Arumí,
E. Martínez-Sáez,
2023,
Journal of Human Genetics.
P. Coubes,
A. Crespel,
P. Gélisse,
2011,
Neurology.
Yoshihiko Saito,
I. Nishino,
S. Ralston,
2023,
Neurology: Genetics.
M. Druet‐Cabanac,
P. Preux,
F. Paraf,
2014,
BMJ Open.
M. Cossée,
F. Leturcq,
Y. Péréon,
2023,
Journal of Neurology.
W. Camu,
R. Juntas-Moralès,
F. Esselin,
2021,
Amyotrophic lateral sclerosis & frontotemporal degeneration.
Annelot M. Dekker,
A. Destée,
S. Bates,
2017,
The Lancet Neurology.
P. Coubes,
A. Crespel,
P. Genton,
2008,
Epilepsia.
J. Glass,
T. Ferguson,
M. Bromberg,
2018,
Clinical Neurophysiology.