Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies-Reference-Cited by-同舟云学术

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Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies

Published:1994-02 Issue:2 Volume:124 Page:224-228
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Rustin Pierre,Lebidois Jerôme,Chretien Dominique,Bourgeron Thomas,Piechaud Jean-François,Rötig Agnès,Munnich Arnold,Sidi Daniel

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference23 articles.

1. Cardiomyopathies;Maron,1992

2. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1;Jarcho;N Engl J Med,1989

3. Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis;Moreadith;J Clin Invest,1984

4. Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondria;Papadimitriou;Pediatr Res,1984

5. Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia;Robinson;J Clin Invest,1986

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