E-LIB Suche - Ergebnisse für: Depienne, C.

1

Identification and characterization of repeat expansions in..:

Leitão, E. ; Schröder, C. ; Depienne, C.
Revue Neurologique. 180 (2024) 5 - p. 383-392 , 2024

Link: https://doi.org/10.1016/..

2

O09 Bi-allelic variants of FILIP1 cause congenital myopathy..:

Roos, A. ; van der Ven, P. ; Alrohaif, H....
Neuromuscular Disorders. 33 (2023) - p. S130 , 2023

Link: https://doi.org/10.1016/..

3

Using medical exome sequencing to identify the causes of ne..:

Chérot, E. ; Keren, B. ; Dubourg, C....
Clinical Genetics. 93 (2017) 3 - p. 567-576 , 2017

Link: https://doi.org/10.1111/..

4

Corpus callosum agenesis with clinically normal people caus..:

Billette de Villemeur, T. ; Valence, S. ; Heron, D....
European Journal of Paediatric Neurology. 21 (2017) - p. e43 , 2017

Link: https://doi.org/10.1016/..

5

A rare case of SPG11 mutation with multiple sclerosis:

Laurencin, C. ; Rascle, L. ; Cotton, F....
Revue Neurologique. 172 (2016) 6-7 - p. 389-391 , 2016

Link: https://doi.org/10.1016/..

6

Clinical and genetic heterogeneity in hereditary spastic pa..:

Klebe, S. ; Stevanin, G. ; Depienne, C.
Revue Neurologique. 171 (2015) 6-7 - p. 505-530 , 2015

Link: https://doi.org/10.1016/..

7

Epilepsy genetics: The ongoing revolution:

Lesca, G. ; Depienne, C.
Revue Neurologique. 171 (2015) 6-7 - p. 539-557 , 2015

Link: https://doi.org/10.1016/..

8

PRRT2 mutations and paroxysmal disorders:

Méneret, A. ; Gaudebout, C. ; Riant, F....
European Journal of Neurology. 20 (2013) 6 - p. 872-878 , 2013

Link: https://doi.org/10.1111/..

9

Épisodes sensitifs et/ou moteurs brachiofaciaux prolongés, ..:

Aubert, S. ; Moncla, A. ; Philip, N....
Revue Neurologique. 169 (2013) - p. A16 , 2013

Link: https://doi.org/10.1016/..

10

Spastic paraplegia gene 7 in patients with spasticity and/o..:

Klebe, S. ; Depienne, C. ; Gerber, S....
Basal Ganglia. 3 (2013) 1 - p. 66 , 2013

Link: https://doi.org/10.1016/..

11

Analysis of the chromosome X exome in patients with autism ..:

Nava, C ; Lamari, F ; Héron, D...
Translational Psychiatry. 2 (2012) 10 - p. e179-e179 , 2012

Link: https://doi.org/10.1038/..

12

Mitochondrial Morpho-Functional Dysfunction in SPG31 Patien..:

Goizet, C. ; Benard, G. ; Depienne, C....
Neurology. 78 (2012) Meeting Abstracts 1 - p. P01.206-P01.206 , 2012

Link: https://doi.org/10.1212/..

13

Novel SPG10 Mutation Associated with Hereditary Spastic Par..:

Collongues, N. ; Depienne, C. ; Boehm, N....
Neurology. 78 (2012) Meeting Abstracts 1 - p. P05.194-P05.194 , 2012

Link: https://doi.org/10.1212/..

14

Mitochondrial Morpho-Functional Dysfunction in SPG31 Patien..:

Goizet, C. ; Benard, G. ; Depienne, C....
Neurology. 78 (2012) Meeting Abstracts 1 - p. IN7-1.007-IN7-1.007 , 2012

Link: https://doi.org/10.1212/..

15

Novel SPG10 mutation associated with dysautonomia, spinal c..:

Collongues, N. ; Depienne, C. ; Boehm, N....
European Journal of Neurology. 20 (2012) 2 - p. 398-401 , 2012

Link: https://doi.org/10.1111/..