(Q70182429)

English

Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study

scientific article published on 01 January 1983

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scholarly article

1 reference

Europe PubMed Central

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9 October 2019

Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6318426%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

author name string

J Müller-Höcker

1

1 reference

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9 October 2019

D Pongratz

2

1 reference

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9 October 2019

G Hübner

3

1 reference

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9 October 2019

publication date

1 January 1983

1 reference

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9 October 2019

Virchows Archiv. A, Pathological Anatomy and Histopathology

1 reference

Europe PubMed Central

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9 October 2019

402

1 reference

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9 October 2019

61-71

1 reference

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9 October 2019

1

1 reference

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9 October 2019

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extraocular muscle biopsy in chronic progressive external ophthalmoplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The significance of ragged-red fibres in neuromuscular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome-c-oxidase deficiency in a floppy infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular disorders with abnormal muscle mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial abnormalities of late motor neuron degeneration following poliomyelitis and other neurogenic muscular atrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. II. Ultrastructure

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Giant Mitochondria in Human Muscle With Inclusions

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytochrome-related inherited disorder of the nervous system and muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial cardiomyopathy with involvement of skeletal muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of cytosolic and mitochondrial enzyme alterations in the livers of propionic or methylmalonic acidemia: a reduction of cytochrome oxidase activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial abnormalities in progressive external ophthalmoplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle biopsy in progressive external ophthalmoplegia (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trichopoliodystrophy. I. Report of a case and biochemical studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6318426

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00695049

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6318426%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6318426%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

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