Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation-Reference-Cited by-同舟云学术

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Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation

Published:2003-12-10 Issue:1 Volume:65 Page:64-65
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Petruzzella V,Zoccolella S,Amati A,Torraco A,Lamberti P,Carnicella F,Serlenga L,Papa S

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. MELAS: an original case and clinical criteria for diagnosis;Hirano;Neuromuscul Disord,1992

2. Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy;Cellini;Brain Res Bull,2001

3. Clinical features and classification of inherited ataxias;Harding;Brain Res Bull,1993

4. Metabolic and Mitochondrial Ataxias

5. Neuronal degeneration and mitochondrial dysfunction;Schon;J Clin Invest,2003

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1. Mitochondrial Disorders;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05

2. Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS);Diagnosis and Management of Mitochondrial Disorders;2019

3. Mitochondrial Neurodegenerative Disorders II: Ataxia, Dystonia and Leukodystrophies;Diagnosis and Management of Mitochondrial Disorders;2019

4. Cerebral imaging in paediatric mitochondrial disorders;The Neuroradiology Journal;2018-07-06

5. Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation;Internal Medicine;2017

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