Histochemical and ultrastructural analysis of the mitochondrial changes in a familial mitochondrial myopathy (Q72625587)

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27 October 2019

title

Histochemical and ultrastructural analysis of the mitochondrial changes in a familial mitochondrial myopathy (English)

1 reference

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27 October 2019

main subject

mitochondrial myopathy

1 reference

1 reference

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18 August 2023

author name string

S. Tassin

1

1 reference

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18 August 2023

G. F. Walter

2

1 reference

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18 August 2023

J. M. Brucher

3

1 reference

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18 August 2023

J. J. Rousseau

4

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18 August 2023

language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6161318

18 August 2023

publication date

1 September 1980

1 reference

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full work available at URL

27 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2990.1980.tb00670.x

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http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.1980.tb00670.x/fullpdf

18 August 2023

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Neuropathology and Applied Neurobiology

18 August 2023

published in

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27 October 2019

volume

6

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27 October 2019

issue

5

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27 October 2019

page(s)

337-347

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Morphologic features of hypermetabolic mitochondrial disease. A light microscopic, histochemical and electron microscopic study

27 October 2019

cites work

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Experimental (-) emetine myopathy. Ultrastructural and morphometric observations

18 August 2023

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Ragged-red fibers. A biochemical and morphological study

18 August 2023

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Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria

18 August 2023

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Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria.

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A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness

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Mitochondrial changes in ischemic skeletal muscle

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Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

18 August 2023

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The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin

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Paracrystalline arrays in mitochondria

18 August 2023

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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

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Experimental mitochondrial myopathy produced by in vivo uncoupling of oxidative phosphorylation

18 August 2023

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A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.

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A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

18 August 2023

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Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism

18 August 2023

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On the pathogenesis of mitochondrial myopathies. An experimental study

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Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease

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Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

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A new mitochondrial myopathy in a patient with salt craving.

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Myopathy with mitochondrial inclusion bodies: histological and metabolic studies

18 August 2023

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Chronic lactic acidosis in association with myopathy

18 August 2023

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Skeletal muscle disease with abnormal mitochondria

18 August 2023

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Use of acridine-orange fluorescence technique in exfoliative cytology

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Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings

18 August 2023

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18 August 2023

Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6161318%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference