Vital A - Search Results

1

Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum.

Vital A, Lepreux S, Vital C. Vital A, et al. Among authors: vital c. J Peripher Nerv Syst. 2014 Dec;19(4):333-42. doi: 10.1111/jns.12099. J Peripher Nerv Syst. 2014. PMID: 25582874 Review.

2

Parkinsonism in a patient with Leber hereditary optic neuropathy (LHON).

Vital C, Julien J, Martin-Negrier ML, Lagueny A, Ferrer X, Vital A. Vital C, et al. Among authors: vital a. Rev Neurol (Paris). 2015 Sep;171(8-9):679-80. doi: 10.1016/j.neurol.2015.03.011. Epub 2015 Apr 24. Rev Neurol (Paris). 2015. PMID: 25917160 Review. No abstract available.

3

[Neuropathological aspects of peripheral nervous system vasculitis].

Vital A, Vital C. Vital A, et al. Among authors: vital c. Rev Neurol (Paris). 2008 Apr;164 Spec No 2:F126-30. Rev Neurol (Paris). 2008. PMID: 18680830 Review. French. No abstract available.

4

Central nervous system lymphomas.

Loiseau H, Cuny E, Vital A, Cohadon F. Loiseau H, et al. Among authors: vital a. Adv Tech Stand Neurosurg. 2000;26:79-124. doi: 10.1007/978-3-7091-6323-8_3. Adv Tech Stand Neurosurg. 2000. PMID: 10997198 Review. No abstract available.

5

High-grade B-cell cerebral lymphoma in a patient with anti-myelin-associated glycoprotein IgM paraproteinemic neuropathy.

Ellie E, Vital A, Steck AJ, Julien J, Henry P, Vital C. Ellie E, et al. Among authors: vital a, vital c. Neurology. 1995 Feb;45(2):378-81. doi: 10.1212/wnl.45.2.378. Neurology. 1995. PMID: 7531825

6

TWINKLE gene mutation: report of a French family with an autosomal dominant progressive external ophthalmoplegia and literature review.

Martin-Negrier ML, Sole G, Jardel C, Vital C, Ferrer X, Vital A. Martin-Negrier ML, et al. Among authors: vital a, vital c. Eur J Neurol. 2011 Mar;18(3):436-41. doi: 10.1111/j.1468-1331.2010.03171.x. Epub 2010 Sep 29. Eur J Neurol. 2011. PMID: 20880070 Review.

7

Endogenous morphine-like compound immunoreactivity increases in parkinsonism.

Charron G, Doudnikoff E, Laux A, Berthet A, Porras G, Canron MH, Barroso-Chinea P, Li Q, Qin C, Nosten-Bertrand M, Giros B, Delalande F, Van Dorsselaer A, Vital A, Goumon Y, Bezard E. Charron G, et al. Among authors: vital a. Brain. 2011 Aug;134(Pt 8):2321-38. doi: 10.1093/brain/awr166. Epub 2011 Jul 8. Brain. 2011. PMID: 21742735

8

Atypical parkinsonism combining alpha-synuclein inclusions and polyglucosan body disease.

Krim E, Vital A, Macia F, Yekhlef F, Tison F. Krim E, et al. Among authors: vital a. Mov Disord. 2005 Feb;20(2):200-4. doi: 10.1002/mds.20285. Mov Disord. 2005. PMID: 15382212

9

Astrocytosis in parkinsonism: considering tripartite striatal synapses in physiopathology?

Charron G, Doudnikoff E, Canron MH, Li Q, Véga C, Marais S, Baufreton J, Vital A, Oliet SH, Bezard E. Charron G, et al. Among authors: vital a. Front Aging Neurosci. 2014 Sep 24;6:258. doi: 10.3389/fnagi.2014.00258. eCollection 2014. Front Aging Neurosci. 2014. PMID: 25309435 Free PMC article.

10

Severe Charcot-Marie-Tooth disease type 1E caused by a novel p.Phe84Leufs*24 PMP22 point mutation.

Vital A, Sole G, Casenave P, Magdelaine C, Ferrer X, Vital C, Goizet C. Vital A, et al. Among authors: vital c. J Peripher Nerv Syst. 2013 Jun;18(2):181-4. doi: 10.1111/jns5.12028. J Peripher Nerv Syst. 2013. PMID: 23781966

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