Vital A - Search Results

1

[Diagnostic procedure of limb girdle muscular dystrophies 2A or calpainopathies: French cohort from a neuromuscular center (Bordeaux)].

Perez F, Vital A, Martin-Negrier ML, Ferrer X, Sole G. Perez F, et al. Among authors: vital a. Rev Neurol (Paris). 2010 May;166(5):502-8. doi: 10.1016/j.neurol.2009.10.015. Epub 2009 Dec 30. Rev Neurol (Paris). 2010. PMID: 20044116 French.

2

[POEMS syndrome (or Crow-Fukase syndrome)].

Lagueny A, Bouillot S, Vital C, Ferrer X, Larrieu JM, Vital A. Lagueny A, et al. Among authors: vital a, vital c. Rev Neurol (Paris). 2004 Mar;160(3):285-95. doi: 10.1016/s0035-3787(04)70903-0. Rev Neurol (Paris). 2004. PMID: 15037841 Review. French.

3

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.

4

Systemic capillary leak syndrome in an 85-year-old man (Clarkson's syndrome).

Bouchet JL, Vital C, Ferrer X, Vital A. Bouchet JL, et al. Among authors: vital a, vital c. Rev Neurol (Paris). 2014 Nov;170(11):713-4. doi: 10.1016/j.neurol.2014.05.010. Epub 2014 Oct 5. Rev Neurol (Paris). 2014. PMID: 25287734 No abstract available.

5

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.

6

A French family with Charcot-Marie-Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations.

Vital A, Latour P, Sole G, Ferrer X, Rouanet M, Tison F, Vital C, Goizet C. Vital A, et al. Among authors: vital c. Neuromuscul Disord. 2012 Aug;22(8):735-41. doi: 10.1016/j.nmd.2012.04.001. Epub 2012 Apr 28. Neuromuscul Disord. 2012. PMID: 22546700

7

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

8

[Hypothyroid neuropathy].

Lagueny A, Manciet G, Vital A, Ferrer X, Julien J. Lagueny A, et al. Among authors: vital a. Rev Neurol (Paris). 1990;146(3):205-10. Rev Neurol (Paris). 1990. PMID: 2158667 French.

9

Paraneoplastic dermatomyositis with glycogen accumulation in muscle.

Lagueny A, Martin-Negrier ML, Bredin A, Berge-Lefranc JL, Piraud M, Vital A. Lagueny A, et al. Among authors: vital a. Rev Neurol (Paris). 2014 Mar;170(3):229-30. doi: 10.1016/j.neurol.2013.09.009. Epub 2014 Mar 6. Rev Neurol (Paris). 2014. PMID: 24613475 No abstract available.

10

Peripheral neuropathy associated with mitochondrial disorders: 8 cases and review of the literature.

Bouillot S, Martin-Négrier ML, Vital A, Ferrer X, Lagueny A, Vincent D, Coquet M, Orgogozo JM, Bloch B, Vita C. Bouillot S, et al. Among authors: vital a. J Peripher Nerv Syst. 2002 Dec;7(4):213-20. doi: 10.1046/j.1529-8027.2002.02027.x. J Peripher Nerv Syst. 2002. PMID: 12477166 Review.

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