Progressive cerebral vascular degeneration with mitochondrial encephalopathy-Reference-Cited by-同舟云学术

Progressive cerebral vascular degeneration with mitochondrial encephalopathy

Published:2008 Issue:3 Volume:146A Page:361-367
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Longo Nicola,Schrijver Iris,Vogel Hannes,Pique Lynn M.,Cowan Tina M.,Pasquali Marzia,Steinberg Gary K.,Hedlund Gary L.,Ernst Sharon L.,Gallagher Renata C.,Enns Gregory M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency*

2. Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement

3. Mitochondrial Angiopathy in a Family with MELAS

4. Endothelial dysfunction in MELAS improved by l-arginine supplementation

5. Mitochondrial encephalopathy

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