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Camuzat, A.
611
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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
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/..
?
3
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/..
?
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
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/..
?
10
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/..
?
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/..
1-15