Mitochondrial myopathy and cardiomyopathy in siblings-Reference-Cited by-同舟云学术

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Mitochondrial myopathy and cardiomyopathy in siblings

Published:1989-05 Issue:3 Volume:5 Page:182-189
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Tulinius Már H.,Eriksson Bengt O.,Hjalmarson Ola,Holme Elisabeth,Oldfors Anders

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference59 articles.

1. Fatal infantile cytochrome c oxidase deficiency: Decrease of immunologically detectable enzyme in muscle;Bresolin;Neurology,1985

2. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency;DiMauro;Neurology,1980

3. Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency;DiMauro;Ann Neurol,1983

4. Cytochrome-c-oxidase deficiency in a floppy infant;Heiman-Patterson;Neurology,1982

5. A patient with lactic acidemia and cytochrome oxidase deficiency;Trijbels;J Inherited Metab Dis,1983

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Muscle Involvement and Restricted Disorders;Volpe's Neurology of the Newborn;2018

2. Mitochondrial encoded NADH dehydrogenase 5 (MT-ND5) gene point mutation presents as late onset cardiomyopathy;International Journal of Cardiology;2013-09

3. Neuromuscular Disorders: Muscle Involvement and Restricted Disorders;Neurology of the Newborn;2008

4. Mitochondrial disorders of the nervous system: Clinical, biochemical, and molecular genetic features;International Review of Neurobiology;2002

5. Treatment of Mitochondrial Cytopathies;Seminars in Neurology;2001

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