Mitochondrial encephalomyopathy with autosomal dominant inheritance: A clinical and genetic entity of mitochondrial diseases-Reference-Cited by-同舟云学术

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Mitochondrial encephalomyopathy with autosomal dominant inheritance: A clinical and genetic entity of mitochondrial diseases

Published:1995-07 Issue:7 Volume:18 Page:753-760
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Kawai Hisaomi,Akaike Masashi,Yokoi Kenji,Nishida Yoshihiko,Kunishige Makoto,Mine Hideki,Saito Shiro

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference28 articles.

1. Ophthalmoplegia-plus, a real nosological entity

2. Fatal infantile cytochrome c oxidase deficiency: Decrease of immunologically detectable enzyme in muscle

3. A mammalian Mitochondrial RNA Processing Activity Contains Nucleus-Encoded RNA

4. Replication and Transcription of Vertebrate Mitochondrial DNA

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1. Mitochondrial myopathies diagnosed in adulthood: clinico-genetic spectrum and long-term outcomes;Brain Communications;2024

2. Mitochondrial mutations in 12S rRNA and 16S rRNA presenting as chronic progressive external ophthalmoplegia (CPEO) plus;Medicine;2017-12

3. Genetics of Mitochondrial Disease;Advances in Genetics;2017

4. Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions;Neurology Genetics;2016-10-19

5. Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A>G point mutation;Neuropathology;2014-11-06

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