Literature DB >> 2646519

Mitochondrial diseases.

M Zeviani1, E Bonilla, D C DeVivo, S DiMauro.   

Abstract

Mitochondrial diseases, and particularly mitochondrial myopathies or encephalomyopathies, have drawn increasing attention in the past decade. Initially defined by morphologic changes in muscle ("ragged red fibers" and ultrastructural abnormalities of mitochondria), mitochondrial encephalomyopathies can now be classified according to biochemical defects involving: (1) mitochondrial transport; (2) substrate oxidation; (3) Krebs cycle; (4) respiratory chain; and (5) oxidation-phosphorylation coupling. For each biochemical group of disorders, the authors describe clinical presentations and biochemical findings. These disorders are especially interesting from the genetic point of view because mitochondria have their own DNA (mtDNA), which encodes 13 polypeptides, all of them subunits of respiratory chain complexes. Other mitochondrial proteins are encoded by nuclear DNA, synthesized in the cytoplasm, and imported into the mitochondria by a complex mechanism. Because mtDNA is inherited strictly by maternal, cytoplasmic inheritance, mitochondrial diseases can be transmitted by Mendelian or by non-Mendelian, maternal inheritance, as illustrated by human pathology.

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Year:  1989        PMID: 2646519

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  12 in total

1.  Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.

Authors:  T P Melo; J M Ferro
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-12       Impact factor: 10.154

2.  A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.

Authors:  A Seyda; R F Newbold; T J Hudson; A Verner; N MacKay; S Winter; A Feigenbaum; S Malaney; D Gonzalez-Halphen; A P Cuthbert; B H Robinson
Journal:  Am J Hum Genet       Date:  2001-01-10       Impact factor: 11.025

Review 3.  Myoclonus and epilepsies.

Authors:  N Fejerman
Journal:  Indian J Pediatr       Date:  1997 Sep-Oct       Impact factor: 1.967

4.  Mitochondrial creatine kinase: a major constituent of pathological inclusions seen in mitochondrial myopathies.

Authors:  A M Stadhouders; P H Jap; H P Winkler; H M Eppenberger; T Wallimann
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

Review 5.  Creatine metabolism and the consequences of creatine depletion in muscle.

Authors:  M Wyss; T Wallimann
Journal:  Mol Cell Biochem       Date:  1994 Apr-May       Impact factor: 3.396

6.  Visual dysfunction in patients with mitochondrial myopathies. I. Electrophysiologic impairments.

Authors:  G Ambrosio; R De Marco; L Loffredo; A Magli
Journal:  Doc Ophthalmol       Date:  1995       Impact factor: 2.379

7.  Visual dysfunction in patients with mitochondrial myopathies. II. Contrast sensitivity function.

Authors:  G Ambrosio; U Giani; L Loffredo; R De Marco; P Vastarella
Journal:  Doc Ophthalmol       Date:  1995       Impact factor: 2.379

8.  Familial visceral myopathy associated with a mitochondrial myopathy.

Authors:  R Lowsky; G Davidson; S Wolman; K N Jeejeebhoy; R A Hegele
Journal:  Gut       Date:  1993-02       Impact factor: 23.059

9.  Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.

Authors:  M K Salo; J Rapola; H Somer; H Pihko; M Koivikko; H J Tritschler; S DiMauro
Journal:  Arch Dis Child       Date:  1992-08       Impact factor: 3.791

10.  Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.

Authors:  R G Haller; K G Henriksson; L Jorfeldt; E Hultman; R Wibom; K Sahlin; N H Areskog; M Gunder; K Ayyad; C G Blomqvist
Journal:  J Clin Invest       Date:  1991-10       Impact factor: 14.808

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