Literature DB >> 8777918

Clinical presentations and laboratory investigations in respiratory chain deficiency.

A Munnich1, A Rötig, D Chretien, J M Saudubray, V Cormier, P Rustin.   

Abstract

Respiratory chain deficiencies have long been regarded as neuromuscular diseases. In fact, oxidative phosphorylation, i.e., ATP synthesis by the respiratory chain not only occurs in the neuromuscular system, indeed, a number of non-neuromuscular organs and tissues are dependent upon mitochondrial energy supply. For this reason, a respiratory chain deficiency can theoretically give rise to any symptom, in any organ or tissue, at any age with any mode of inheritance, due to the twofold genetic origin of respiratory enzymes (nuclear DNA and mitochondrial DNA).

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Year:  1996        PMID: 8777918     DOI: 10.1007/bf02002711

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  26 in total

1.  Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Authors:  A Rötig; V Cormier; S Blanche; J P Bonnefont; F Ledeist; N Romero; J Schmitz; P Rustin; A Fischer; J M Saudubray
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

2.  Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis.

Authors:  J P Bonnefont; D Chretien; P Rustin; B Robinson; A Vassault; J Aupetit; C Charpentier; D Rabier; J M Saudubray; A Munnich
Journal:  J Pediatr       Date:  1992-08       Impact factor: 4.406

3.  Hepatic failure in disorders of oxidative phosphorylation with neonatal onset.

Authors:  V Cormier; P Rustin; J P Bonnefont; C Rambaud; A Vassault; D Rabier; P Parvy; S Couderc; F Parrot-Roulaud; M Carré
Journal:  J Pediatr       Date:  1991-12       Impact factor: 4.406

4.  A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Authors:  I J Holt; A E Harding; R K Petty; J A Morgan-Hughes
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

5.  Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies.

Authors:  P Rustin; J Lebidois; D Chretien; T Bourgeron; J F Piechaud; A Rötig; A Munnich; D Sidi
Journal:  J Pediatr       Date:  1994-02       Impact factor: 4.406

6.  Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.

Authors:  T Bourgeron; P Rustin; D Chretien; M Birch-Machin; M Bourgeois; E Viegas-Péquignot; A Munnich; A Rötig
Journal:  Nat Genet       Date:  1995-10       Impact factor: 38.330

7.  Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia.

Authors:  A Rötig; J L Bessis; N Romero; V Cormier; J M Saudubray; P Narcy; G Lenoir; P Rustin; A Munnich
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

8.  Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiency.

Authors:  B Chabrol; J Mancini; D Chretien; P Rustin; A Munnich; N Pinsard
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

9.  Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.

Authors:  J Vilkki; J Ott; M L Savontaus; P Aula; E K Nikoskelainen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

10.  An autosomal locus predisposing to deletions of mitochondrial DNA.

Authors:  A Suomalainen; J Kaukonen; P Amati; R Timonen; M Haltia; J Weissenbach; M Zeviani; H Somer; L Peltonen
Journal:  Nat Genet       Date:  1995-02       Impact factor: 38.330

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  28 in total

Review 1.  Inborn errors of metabolism as a cause of neurological disease in adults: an approach to investigation.

Authors:  R G Gray; M A Preece; S H Green; W Whitehouse; J Winer; A Green
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-07       Impact factor: 10.154

2.  Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases.

Authors:  B Korzeniewski; M Malgat; T Letellier; J P Mazat
Journal:  Biochem J       Date:  2001-08-01       Impact factor: 3.857

Review 3.  Laboratory approach to mitochondrial diseases.

Authors:  D Parra; A González; C Mugueta; A Martínez; I Monreal
Journal:  J Physiol Biochem       Date:  2001-09       Impact factor: 4.158

4.  Multiple presentation of mitochondrial disorders.

Authors:  A Nissenkorn; A Zeharia; D Lev; A Fatal-Valevski; V Barash; A Gutman; S Harel; T Lerman-Sagie
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

5.  Introduction of an additional pathway for lactate oxidation in the treatment of lactic acidosis and mitochondrial dysfunction in Caenorhabditis elegans.

Authors:  Leslie I Grad; Leanne C Sayles; Bernard D Lemire
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-12       Impact factor: 11.205

6.  Mitochondrial respiratory chain hepatopathies: role of liver transplantation. A case series of five patients.

Authors:  Elisabeth De Greef; John Christodoulou; Ian E Alexander; Albert Shun; Edward V O'Loughlin; David R Thorburn; Vicki Jermyn; Michael O Stormon
Journal:  JIMD Rep       Date:  2011-11-04

7.  Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy.

Authors:  H Li; J Wang; H Wilhelmsson; A Hansson; P Thoren; J Duffy; P Rustin; N G Larsson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-28       Impact factor: 11.205

8.  A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.

Authors:  M Jaksch; S Hofmann; S Kleinle; S Liechti-Gallati; D E Pongratz; J Müller-Höcker; K B Jedele; T Meitinger; K D Gerbitz
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

Review 9.  Mouse models of oxidative phosphorylation defects: powerful tools to study the pathobiology of mitochondrial diseases.

Authors:  Alessandra Torraco; Francisca Diaz; Uma D Vempati; Carlos T Moraes
Journal:  Biochim Biophys Acta       Date:  2008-06-13

10.  Next generation sequence analysis for mitochondrial disorders.

Authors:  Valeria Vasta; Sarah B Ng; Emily H Turner; Jay Shendure; Si Houn Hahn
Journal:  Genome Med       Date:  2009-10-23       Impact factor: 11.117

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