(Q44583856)

4 December 2017

title

Late onset of stroke-like episode associated with a 3256C-->T point mutation of mitochondrial DNA. (English)

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4 December 2017

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Tina Dysgaard Jeppesen

1

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4 December 2017

Marianne Schwartz

2

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4 December 2017

Klaus Hansen

3

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4 December 2017

Else R Danielsen

4

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4 December 2017

Flemming Wibrand

5

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4 December 2017

John Vissing

6

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4 December 2017

publication date

1 October 2003

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Journal of the Neurological Sciences

4 December 2017

number of pages

4

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based on heuristic

inferred from page(s)

published in

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4 December 2017

volume

214

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4 December 2017

issue

1-2

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4 December 2017

page(s)

17-20

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Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

4 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Mitochondria in neuromuscular disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

MELAS: clinical features, biochemistry, and molecular genetics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulin-dependent diabetes mellitus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Oxidative capacity correlates with muscle mutation load in mitochondrial myopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

Quantitative proton magnetic resonance spectroscopy of cerebral metabolic disturbances in patients with MELAS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900168-0

10.1016/S0022-510X(03)00168-0

7 January 2021

Identifiers

DOI

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4 December 2017

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