E-LIB Suche - Ergebnisse für: Camuzat, A.

1

FROM THE SPINAL CORD TO THE MUSCLE:

Querin, G. ; Bede, P. ; Mendili, M. El...
Neuromuscular Disorders. 30 (2020) - p. S148 , 2020

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

2

Frequency and Phenotypes Associated with C9ORF72 Repeat Exp..:

Le Ber, I. ; Camuzat, A. ; Guillot-Noel, L....
Neurology. 78 (2012) Meeting Abstracts 1 - p. S54.003-S54.003 , 2012

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

3

Fréquence et phénotypes associés aux mutations du gène c9or..:

Le Ber, I. ; Camuzat, A. ; Hannequin, D....
Revue Neurologique. 168 (2012) - p. A196 , 2012

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

4

Chromosome 9p-linked families with frontotemporal dementia ..:

Le Ber, I. ; Camuzat, A. ; Berger, E....
Neurology. 72 (2009) 19 - p. 1669-1676 , 2009

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

5

Exhaustive analysis of BH4 and dopamine biosynthesis genes ..:

Clot, F. ; Grabli, D. ; Cazeneuve, C....
Brain. 132 (2009) 7 - p. 1753-1763 , 2009

Link: https://doi.org/10.1093/..

6

Mutations du gène de la progranuline dans les démences fron..:

Le Ber, I. ; Camuzat, A. ; Hannequin, D....
Revue Neurologique. 163 (2007) 4 - p. 207-208 , 2007

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

7

Are interruptedSCA2CAG repeat expansions responsible for pa..:

Charles, P. ; Camuzat, A. ; Benammar, N....
Neurology. 69 (2007) 21 - p. 1970-1975 , 2007

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

8

Clinical and neuropathologic study of a French family with ..:

Gourfinkel-An, I. ; Duyckaerts, C. ; Camuzat, A....
Neurology. 69 (2007) 1 - p. 79-83 , 2007

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

9

Demographic, neurological and behavioural characteristics a..:

Ber, I. L. ; Guedj, E. ; Gabelle, A....
Brain. 129 (2006) 11 - p. 3051-3065 , 2006

Link: https://doi.org/10.1093/..

10

Predominant dystonia with marked cerebellar atrophy: A rare..:

Le Ber, I. ; Clot, F. ; Vercueil, L....
Neurology. 67 (2006) 10 - p. 1769-1773 , 2006

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

11

Frontotemporal dementia, motor neuron disease and tauopathy..:

Martinaud, O. ; Laquerrière, A. ; Guyant-Maréchal, L....
Acta Neuropathologica. 110 (2005) 1 - p. 84-92 , 2005

Link: https://doi.org/10.1007/..

12

CAG/CTG repeat expansions at the Huntington's disease–like ..:

Stevanin, G. ; Camuzat, A. ; Holmes, S. E....
Neurology. 58 (2002) 6 - p. 965-967 , 2002

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

13

Genomic Organization of the Human SPOCK Gene and Its Chromo..:

Charbonnier, F ; Périn, J-P ; Mattei, M-G...
Genomics. 48 (1998) 3 - p. 377-380 , 1998

Link: https://doi.org/10.1006/..

14

Segregation of a Missense Mutation in the Microtubule-Assoc..:

Dumanchin, C. ; Camuzat, A. ; Campion, D....
Human Molecular Genetics. 7 (1998) 11 - p. 1825-1829 , 1998

Link: https://doi.org/10.1093/..

15

Evidence of genetic heterogeneity of Leber's congenital ama..:

Camuzat, A. ; Rozet, J. -M. ; Dollfus, H....
Human Genetics. 97 (1996) 6 - p. 798-801 , 1996

Link: https://doi.org/10.1007/..