(Q33676556)

28 July 2017

Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study (English)

1 reference

28 July 2017

0 references

1 reference

Drugge U

1

1 reference

28 July 2017

Holmberg M

2

1 reference

28 July 2017

Holmgren G

3

1 reference

28 July 2017

Almay BG

4

1 reference

28 July 2017

Linderholm H

5

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28 July 2017

language of work or name

English

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publication date

1 May 1995

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

32

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28 July 2017

5

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28 July 2017

344-347

1 reference

HEREDITARY METABOLIC MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Computer-simulation methods in human linkage analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050427

Hereditary abnormal muscle metabolism with hyperkinetic circulation during exercise

30 October 2018

1 reference

12 December 2020

Amino acid metabolism in patients with a hereditary myopathy and paroxysmal myoglobinuria

1 reference

12 December 2020

Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria

1 reference

12 December 2020

Hereditary myopathy with succinate dehydrogenase deficiency--a rare life-threatening disease

1 reference

12 December 2020

Dependence of maximum performance time on work intensity in patients with a hereditary myopathy with succinate dehydrogenase deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.32.5.344

1 reference

28 July 2017

1 reference

28 July 2017

1 reference