Familial visceral myopathy associated with a mitochondrial myopathy (Q34375623)

1 August 2017

title

Familial visceral myopathy associated with a mitochondrial myopathy (English)

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1 August 2017

main subject

mitochondrial myopathy

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Lowsky R

1

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1 August 2017

Davidson G

2

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1 August 2017

Wolman S

3

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1 August 2017

Jeejeebhoy KN

4

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1 August 2017

Hegele RA

5

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1 August 2017

language of work or name

English

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publication date

1 February 1993

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1 August 2017

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1 August 2017

volume

34

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1 August 2017

issue

2

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1 August 2017

page(s)

279-283

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Sequence and organization of the human mitochondrial genome

1 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Familial autonomic visceral myopathy with degeneration of muscularis mucosae

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Mitochondrial myopathy: a genetic study of 71 cases

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Familial intestinal pseudoobstruction dominated by a progressive neurologic disease at a young age.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Familial visceral myopathy: a family with at least six involved members

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudo-obstruction: POLIP syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Paternal inheritance of mitochondrial DNA in mice

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

Studies of idiopathic intestinal pseudoobstruction. II. Hereditary hollow visceral myopathy: family studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

A familial visceral myopathy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

A case of familial visceral myopathy with atrophy and fibrosis of the longitudinal muscle layer of the entire small bowel

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1373985

A familial visceral myopathy with external ophthalmoplegia and autosomal recessive transmission

6 July 2018

1 reference

12 December 2020

Inherited ophthalmoplegia with intestinal pseudo-obstruction

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12 December 2020

A familial visceral myopathy with dilatation of the entire gastrointestinal tract

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12 December 2020

Apolipoprotein B-gene DNA polymorphisms associated with myocardial infarction

1 reference

12 December 2020

Familial visceral myopathy. Evidence of diffuse involvement of intestinal smooth muscle

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12 December 2020

Mitochondrial diseases

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12 December 2020

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

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12 December 2020

The other human genome

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12 December 2020

Identifiers

DOI

10.1136/GUT.34.2.279

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1 August 2017

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1 August 2017

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