(Q37005220)

English

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

scientific article published on January 1981

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1 reference

based on heuristic

inferred from title

myoclonic epilepsy

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

author name string

Fitzsimons RB

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Clifton-Bligh P

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Wolfenden WH

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

language of work or name

0 references

publication date

1 January 1981

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

44

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

79-82

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

29 September 2017

Lactic acidemia, mitochondrial myopathy, and basal ganglia calcification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

29 September 2017

Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

29 September 2017

Mitochondrial myopathy with multisystem abnormalities and normal ocular movements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

29 September 2017

"Ragged-red" fibers in Leigh's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

27 June 2018

Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

27 June 2018

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490823

4 September 2018

Electrophysiological abnormalities in pigmentary degenerations of the retina. Assessment of value and basis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6782198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Ovular myopathy with primary hypogonadism. Mitochondrial abnormalities in ultrastructural study]

1 reference

https://pubmed.ncbi.nlm.nih.gov/6782198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypothyroid myopathy. Clinical, electromyographical, and ultrastructural observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/6782198

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/6782198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6782198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Depressed ventilatory response in oculocraniosomatic neuromuscular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6782198

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.44.1.79

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

0 references

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