Literature DB >> 3681314

Biochemical studies in mitochondrial encephalomyopathy.

S Goda1, S Ishimoto, I Goto, Y Kuroiwa, K Koike, M Koike, M Nakagawa, H Reichmann, S DiMauro.   

Abstract

The alpha-keto acid dehydrogenase complex and its component enzymes, lactate dehydrogenase, pyruvate carboxylase, cytochrome c oxidase, succinate-cytochrome c reductase, NADH-cytochrome c reductase, and the concentration of cytochromes and enzymes of beta-oxidation in muscle from a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes were studied and no specific defect was found. These results raise the possibility that the mitochondrial changes in the patient may be secondary.

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Year:  1987        PMID： 3681314      PMCID： PMC1032463          DOI： 10.1136/jnnp.50.10.1348

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


  20 in total

1.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases.

Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

2.  Purification and comparative properties of human lactate dehydrogenase isozymes from uterus, uterine myoma, and cervical cancer.

Authors:  K Okabe; T Hayakawa; M Hamada; M Koike
Journal:  Biochemistry       Date:  1968-01       Impact factor: 3.162

3.  Striated muscle ultrastructure in intermittent claudication.

Authors:  H Teräväinen; J Mäkitie
Journal:  Arch Pathol Lab Med       Date:  1977-05       Impact factor: 5.534

4.  Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.

Authors:  M Kuriyama; H Umezaki; Y Fukuda; M Osame; K Koike; J Tateishi; A Igata
Journal:  Neurology       Date:  1984-01       Impact factor: 9.910

5.  Biochemical properties of mammalian 2-oxo acid dehydrogenase multienzyme complexes and clinical relevancy with chronic lactic acidosis.

Authors:  M Koike; K Koike
Journal:  Ann N Y Acad Sci       Date:  1982       Impact factor: 5.691

6.  Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis.

Authors:  Y Kobayashi; S Miyabayashi; G Takada; K Narisawa; K Tada; T Y Yamamoto
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

7.  Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.

Authors:  N Bresolin; M Zeviani; E Bonilla; R H Miller; R W Leech; S Shanske; M Nakagawa; S DiMauro
Journal:  Neurology       Date:  1985-06       Impact factor: 9.910

8.  Reversible alexia, mitochondrial myopathy, and lactic acidemia.

Authors:  R R Skoglund
Journal:  Neurology       Date:  1979-05       Impact factor: 9.910

9.  Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency.

Authors:  C P Trevisan; H Reichmann; D C DeVivo; S DiMauro
Journal:  Muscle Nerve       Date:  1985-10       Impact factor: 3.217

10.  Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Authors:  N Fukuhara; S Tokiguchi; K Shirakawa; T Tsubaki
Journal:  J Neurol Sci       Date:  1980-07       Impact factor: 3.181
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  1 in total

1.  Mitochondrial encephalomyopathy with pilovacuolar inclusion or phenocopy with mitochondrial artefact?

Authors:  W Paulus; A Stevens; W Roggendorf
Journal:  J Neurol       Date:  1989-09       Impact factor: 4.849
  1 in total

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