Mitochondrial Encephalomyopathies: Incidence & DNA

J Gordon Millichap

doi:10.15844/pedneurbriefs-15-3-6

Mitochondrial Encephalomyopathies: Incidence & DNA

Pediatric Neurology Briefs

Volume 15 (2001): Issue 3

By: J Gordon Millichap

Open Access

|Mar 2001

Abstract

The incidence, mortality, clinical features and DNA abnormalities of mitochondrial encephalomyopathies (ME) were evaluated in a population-based study of children from western Sweden conducted at The Queen Silvia Children’s Hospital, Goteborg, Sweden.

References

Darin N Oldfors A Moslemi AR Holme E Tulinius M The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA anbormalities Ann Neurol 2001 Mar 49 3 377 383 10.1002/ana.75 11261513
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Jackson MJ Schaefer JA Johnson MA Morris AA Turnbull DM Bindoff LA Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients Brain 1995 Apr 118 Pt 2 339 357 10.1093/brain/118.2.339 7735877
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-15-3-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 21 - 21

Published on: Mar 1, 2001

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Mitochondrial Encephalomyopathies,

Neurometabolic Disorders,

Ophthalmoplegia

© 2001 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 15 (2001): Issue 3