Literature DB >> 752349

Pyruvate oxidation in rat and human skeletal muscle mitochondria.

H Bookelman, J M Trijbels, R C Sengers, A J Janssen, J H Veerkamp, A M Stadhouders.   

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Year:  1978        PMID： 752349     DOI： 10.1016/0006-2944(78)90089-3

Source DB:  PubMed          Journal:  Biochem Med        ISSN： 0006-2944


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  29 in total

1.  Human quadriceps muscle mitochondria: a functional characterization.

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2.  Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation.

Authors:  Johannes A Mayr; Olaf Merkel; Sepp D Kohlwein; Boris R Gebhardt; Hansjosef Böhles; Ulrike Fötschl; Johannes Koch; Michaela Jaksch; Hanns Lochmüller; Rita Horváth; Peter Freisinger; Wolfgang Sperl
Journal:  Am J Hum Genet       Date:  2007-01-10       Impact factor: 11.025

3.  Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.

Authors:  M Kobayashi; H Morishita; N Sugiyama; K Yokochi; M Nakano; Y Wada; Y Hotta; A Terauchi; I Nonaka
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Authors:  P M Van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; H J Ter Laak; A M Stadhouders
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-05       Impact factor: 10.154

Review 5.  Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach.

Authors:  J M Trijbels; R C Sengers; W Ruitenbeek; J C Fischer; J A Bakkeren; A J Janssen
Journal:  Eur J Pediatr       Date:  1988-11       Impact factor: 3.183

6.  Hypertrophic cardiomyopathy associated with a mitochondrial myopathy of voluntary muscles and congenital cataract.

Authors:  R C Sengers; A M Stadhouders; E van Lakwijk-Vondrovicova; K Kubat; W Ruitenbeek
Journal:  Br Heart J       Date:  1985-11

7.  Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency.

Authors:  R C Sengers; J M Trijbels; J A Bakkeren; W Ruitenbeek; J C Fischer; A J Janssen; A M Stadhouders; H J ter Laak
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

8.  Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.

Authors:  P M van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; K J Lamers; J L Sloof
Journal:  J Neurol       Date:  1987-05       Impact factor: 4.849

9.  The effect of oral supplementation with L-carnitine on maximum and submaximum exercise capacity.

Authors:  C Greig; K M Finch; D A Jones; M Cooper; A J Sargeant; C A Forte
Journal:  Eur J Appl Physiol Occup Physiol       Date:  1987

10.  Demyelination and disturbed metabolism of pyruvate: a case report.

Authors:  R C Sengers; J M Trijbels; J A Bakkeren; W Ruitenbeek; A J Janssen; A M Stadhouders; H J ter Laak
Journal:  Eur J Pediatr       Date:  1983-04       Impact factor: 3.183
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