Verny C - Search Results

1

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.

Cassereau J, Chevrollier A, Gueguen N, Desquiret V, Verny C, Nicolas G, Dubas F, Amati-Bonneau P, Reynier P, Bonneau D, Procaccio V. Cassereau J, et al. Among authors: verny c. Exp Neurol. 2011 Jan;227(1):31-41. doi: 10.1016/j.expneurol.2010.09.006. Epub 2010 Sep 21. Exp Neurol. 2011. PMID: 20849849 Review.

2

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.

Guilbot A, Williams A, Ravisé N, Verny C, Brice A, Sherman DL, Brophy PJ, LeGuern E, Delague V, Bareil C, Mégarbané A, Claustres M. Guilbot A, et al. Among authors: verny c. Hum Mol Genet. 2001 Feb 15;10(4):415-21. doi: 10.1093/hmg/10.4.415. Hum Mol Genet. 2001. PMID: 11157804

3

Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy.

Letournel F, Etcharry-Bouyx F, Verny C, Barthelaix A, Dubas F. Letournel F, et al. Among authors: verny c. J Neurol Neurosurg Psychiatry. 2003 May;74(5):671-3. doi: 10.1136/jnnp.74.5.671. J Neurol Neurosurg Psychiatry. 2003. PMID: 12700318 Free PMC article.

4

[Processing of "scripts" and frontal lobe function in Huntington's disease].

Allain P, Verny C, Aubin G, Bonneau D, Dubas F, Le Gall D. Allain P, et al. Among authors: verny c. Rev Neurol (Paris). 2004 Apr;160(4 Pt 1):434-40. doi: 10.1016/s0035-3787(04)70925-x. Rev Neurol (Paris). 2004. PMID: 15103268 French.

5

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.

Reynier P, Amati-Bonneau P, Verny C, Olichon A, Simard G, Guichet A, Bonnemains C, Malecaze F, Malinge MC, Pelletier JB, Calvas P, Dollfus H, Belenguer P, Malthièry Y, Lenaers G, Bonneau D. Reynier P, et al. Among authors: verny c. J Med Genet. 2004 Sep;41(9):e110. doi: 10.1136/jmg.2003.016576. J Med Genet. 2004. PMID: 15342707 Free PMC article. No abstract available.

6

[Genetics of specific language impairments].

Bonneau D, Verny C, Uzé J. Bonneau D, et al. Among authors: verny c. Arch Pediatr. 2004 Oct;11(10):1213-6. doi: 10.1016/j.arcped.2004.03.121. Arch Pediatr. 2004. PMID: 15475279 Review. French.

7

Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.

Verny C, Ravisé N, Leutenegger AL, Pouplard F, Dubourg O, Tardieu S, Dubas F, Brice A, Genin E, LeGuern E. Verny C, et al. Neurology. 2004 Oct 26;63(8):1527-9. doi: 10.1212/01.wnl.0000142082.65144.ee. Neurology. 2004. PMID: 15505184

8

Arithmetic word-problem-solving in Huntington's disease.

Allain P, Verny C, Aubin G, Pinon K, Bonneau D, Dubas F, Le Gall D. Allain P, et al. Among authors: verny c. Brain Cogn. 2005 Feb;57(1):1-3. doi: 10.1016/j.bandc.2004.08.010. Brain Cogn. 2005. PMID: 15629205 Clinical Trial.

9

Isolated Horner's syndrome may herald stroke.

de Bray JM, Baumgartner R, Guillon B, Pautot V, Dziewas R, Ringelstein EB, Sturzenegger M, Garnier P, Ducrocq X, Saudeau D, Neau JP, Larrue V, Vuillier F, Boulliat J, Verret JM, Verny C, Dubas F. de Bray JM, et al. Among authors: verny c. Cerebrovasc Dis. 2005;19(4):274-5. doi: 10.1159/000084370. Epub 2005 Mar 10. Cerebrovasc Dis. 2005. PMID: 15761221 No abstract available.

10

[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs].

Verny C, Amati-Bonneau P, Dubas F, Malthiéry Y, Reynier P, Bonneau D. Verny C, et al. Rev Neurol (Paris). 2005 Apr;161(4):451-4. doi: 10.1016/s0035-3787(05)85075-1. Rev Neurol (Paris). 2005. PMID: 15924081 French.

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