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Literature DB >> 7753698

Mitochondrial cardiomyopathy.

Abstract

An adolescent with mitochondrial cardiomyopathy is described. Skeletal and cardiac biopsies revealed abnormal mitochondria, with biochemical analysis showing cytochrome c oxidase deficiency.

Entities: Disease

Mesh：

Year: 1995 PMID： 7753698 DOI： 10.1007/BF02310331

Source DB: PubMed Journal: Pediatr Cardiol ISSN： 0172-0643 Impact factor: 1.655

12 in total

1. Mitochondrial mutation in fatal infantile cardiomyopathy.

Authors: M Tanaka; H Ino; K Ohno; K Hattori; W Sato; T Ozawa; T Tanaka; S Itoyama
Journal: Lancet Date: 1990-12-08 Impact factor: 79.321

2. Benign reversible muscle cytochrome c oxidase deficiency: a second case.

Authors: M Zeviani; P Peterson; S Servidei; E Bonilla; S DiMauro
Journal: Neurology Date: 1987-01 Impact factor: 9.910

3. Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Authors: M Zeviani; C Gellera; C Antozzi; M Rimoldi; L Morandi; F Villani; V Tiranti; S DiDonato
Journal: Lancet Date: 1991-07-20 Impact factor: 79.321

4. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy.

Authors: T Ozawa; M Tanaka; S Sugiyama; K Hattori; T Ito; K Ohno; A Takahashi; W Sato; G Takada; B Mayumi
Journal: Biochem Biophys Res Commun Date: 1990-07-31 Impact factor: 3.575

5. An X-linked recessive cardiomyopathy with abnormal mitochondria.

Authors: H B Neustein; P R Lurie; B Dahms; M Takahashi
Journal: Pediatrics Date: 1979-07 Impact factor: 7.124

6. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.

Authors: J Müller-Höcker; D Pongratz; T Deufel; J M Trijbels; W Endres; G Hübner
Journal: Virchows Arch A Pathol Anat Histopathol Date: 1983

Mitochondrial cardiomyopathy.

1. Mitochondrial mutation in fatal infantile cardiomyopathy.

2. Benign reversible muscle cytochrome c oxidase deficiency: a second case.

3. Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

4. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy.

5. An X-linked recessive cardiomyopathy with abnormal mitochondria.

6. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.

7. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.

8. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

9. Mitochondrial genetics: a paradigm for aging and degenerative diseases?

10. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

1. High-salt diet during pregnancy and angiotensin-related cardiac changes.