Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods-Reference-Cited by-同舟云学术

Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods

Published:2006-02 Issue:2 Volume:37 Page:173-184
ISSN:0046-8177
Container-title:Human Pathology
language:en
Short-container-title:Human Pathology

Author:

Miles Lili,Wong Brenda L.,Dinopoulos Argirios,Morehart Paula J.,Hofmann Irene A.,Bove Kevin E.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference32 articles.

1. Neurological presentations of mitochondrial diseases;Zeviani;J Inherit Metab Dis,1996

2. Mitochondrial encephalomyopathies;DiMauro;Arch Neurol,1993

3. Wallace DC. Mitochondrial genes and disease. Hosp Pract 1986;121:77-87, 90-92.

4. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies;Servidei;Neurology,1991

5. Isolated complex I deficiency in children: clinical, biochemical and genetic aspects;Loeffen;Hum Mutat,2000

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