Dubas F - Search Results

1

[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. Among authors: dubas f. Rev Neurol (Paris). 2005 Apr;161(4):451-4. doi: 10.1016/s0035-3787(05)85075-1. Rev Neurol (Paris). 2005. PMID: 15924081 French.

2

[Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].

Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P. Pénisson-Besnier I, et al. Among authors: dubas f. Rev Neurol (Paris). 2001 May;157(5):537-41. Rev Neurol (Paris). 2001. PMID: 11438773 French.

3

[Hereditary optic atrophies].

Scherer C, Procaccio V, Ferre M, Guillet V, Reynier P, Amati-Bonneau P, Dubas F, Bonneau D, Verny C. Scherer C, et al. Among authors: dubas f. Rev Neurol (Paris). 2010 Dec;166(12):959-65. doi: 10.1016/j.neurol.2010.07.033. Epub 2010 Nov 5. Rev Neurol (Paris). 2010. PMID: 21056443 Review. French.

4

Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy.

Lamirel C, Cassereau J, Cochereau I, Vignal-Clermont C, Pajot O, Tanguy JY, Zanlonghi X, Reynier P, Amati-Bonneau P, Dubas F, Bonneau D, Verny C. Lamirel C, et al. Among authors: dubas f. J Neurol Neurosurg Psychiatry. 2010 May;81(5):578-80. doi: 10.1136/jnnp.2009.174953. J Neurol Neurosurg Psychiatry. 2010. PMID: 20460595 Free article.

5

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.

Verny C, Guegen N, Desquiret V, Chevrollier A, Prundean A, Dubas F, Cassereau J, Ferre M, Amati-Bonneau P, Bonneau D, Reynier P, Procaccio V. Verny C, et al. Among authors: dubas f. Mitochondrion. 2011 Jan;11(1):70-5. doi: 10.1016/j.mito.2010.07.006. Epub 2010 Jul 22. Mitochondrion. 2011. PMID: 20656066

6

mtDNA haplogroup J: a contributing factor of optic neuritis.

Reynier P, Penisson-Besnier I, Moreau C, Savagner F, Vielle B, Emile J, Dubas F, Malthièry Y. Reynier P, et al. Among authors: dubas f. Eur J Hum Genet. 1999 Apr;7(3):404-6. doi: 10.1038/sj.ejhg.5200293. Eur J Hum Genet. 1999. PMID: 10234520

7

[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: dubas f. 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.

8

[Idiopathic acute transverse myelitis: application of new diagnosis criteria to 17 patients].

Lanctin C, Wiertlewski S, Moreau C, Verny C, Derkinderen P, Damier P, Dubas F. Lanctin C, et al. Among authors: dubas f. Rev Neurol (Paris). 2006 Oct;162(10):980-9. doi: 10.1016/s0035-3787(06)75108-6. Rev Neurol (Paris). 2006. PMID: 17028566 French.

9

Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.

Verny C, Allain P, Prudean A, Malinge MC, Gohier B, Scherer C, Bonneau D, Dubas F, Le Gall D. Verny C, et al. Among authors: dubas f. Eur J Neurol. 2007 Dec;14(12):1344-50. doi: 10.1111/j.1468-1331.2007.01975.x. Epub 2007 Oct 17. Eur J Neurol. 2007. PMID: 17941857

10

Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy.

Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, Bonneau D. Verny C, et al. Among authors: dubas f. Neurology. 2008 Mar 25;70(13 Pt 2):1152-3. doi: 10.1212/01.wnl.0000289194.89359.a1. Epub 2008 Feb 20. Neurology. 2008. PMID: 18287570 Free article. No abstract available.

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