Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot–Marie–Tooth presentation-Reference-Cited by-同舟云学术

Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot–Marie–Tooth presentation

Published:2005-03-07 Issue:6 Volume:252 Page:655-662
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Said Gérard,Lacroix Catherine,Planté-Bordeneuve Violaine,Messing Bernard,Slama Abdelhamid,Crenn Pascal,Nivelon-Chevallier Annie,Bedenne Laurent,Soichot Pierre,Manceau E.,Rigaud Daniel,Guiochon-Mantel Anne,Matuchansky Claude

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-005-0712-4.pdf

Reference11 articles.

1. Bardosi A, Creutzfeldt W, DiMauro S, et al. (1987) Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder. Acta Neuropathol (Berl) 74:248–258

2. Bedlack RS, Vu T, Hammans S, et al. (2004) MNGIE Neuropathy; Five cases mimicking chronic inflammatory demyelinating polyneuropathy. Muscle Nerve 29:364–368

3. Carrozzo R, Hirano M, Fromenty B, et al. (1998) Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses. Neurology 50:99–106

4. Debouverie M, Wagner M, Ducrocq X, et al. (1997) MNGIE syndrome in 2 siblings. Rev Neurol (Paris) 153:547–553

5. Gamez J, Ferreiro C, Accarino ML, et al. (2002) Phenotypic variability in a Spanish family with MNGIE. Neurology 59:455–457

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