Biochemical studies in mitochondrial encephalomyopathy (Q33629607)

28 July 2017

Biochemical studies in mitochondrial encephalomyopathy (English)

1 reference

mitochondrial encephalomyopathy

28 July 2017

1 reference

Goda S

1

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28 July 2017

Ishimoto S

2

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28 July 2017

Goto I

3

1 reference

28 July 2017

Kuroiwa Y

4

1 reference

28 July 2017

Koike K

5

1 reference

28 July 2017

Koike M

6

1 reference

28 July 2017

Nakagawa M

7

1 reference

28 July 2017

Reichmann H

8

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28 July 2017

DiMauro S

9

1 reference

28 July 2017

language of work or name

English

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publication date

1 October 1987

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

28 July 2017

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28 July 2017

50

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28 July 2017

10

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28 July 2017

1348-1352

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

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Striated muscle ultrastructure in intermittent claudication

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Pyruvate Carboxylase and Phosphoenolpyruvate Carboxykinase Activity in Leukocytes and Fibroblasts from a Patient with Pyruvate Carboxylase Deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Crystals in muscle fibers in patients with diabetic amyotrophy and neuropathy

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

Reversible alexia, mitochondrial myopathy, and lactic acidemia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032463

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

30 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypothyroid myopathy. Clinical, electromyographical, and ultrastructural observations

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.50.10.1348

1 reference

28 July 2017

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28 July 2017

1 reference