(Q35560836)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

review article

1 reference

title

116th ENMC international workshop: the treatment of mitochondrial disorders, 14th-16th March 2003, Naarden, The Netherlands (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

0 references

0 references

Europen neuromuscular center

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

language of work or name

1 reference

1 November 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

published in

Neuromuscular Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

page(s)

757-764

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

The epidemiology of pathogenic mitochondrial DNA mutations

20 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Epidemiology and treatment of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Near-infrared spectroscopy in chronic progressive external ophthalmoplegia: adipose tissue thickness confounds decreased muscle oxygen consumption

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by31P magnetic resonance spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Antioxidant treatment improves in vivo cardiac and skeletal muscle bioenergetics in patients with Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Reversal of a mitochondrial DNA defect in human skeletal muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Gene shifting: a novel therapy for mitochondrial myopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2803%2900097-X

7 January 2021

10.1016/S0960-8966(03)00097-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14561500%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference