A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome. (Q53537772)

15 May 2018

title

A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome. (English)

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15 May 2018

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mitochondrial myopathy

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Jie-Yuan Li

1

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15 May 2018

Rong-Hong Hsieh

2

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15 May 2018

Nan-Jing Peng

3

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15 May 2018

Ping-Hong Lai

4

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15 May 2018

Cheng-Feng Lee

5

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15 May 2018

Yuk-Keung Lo

6

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15 May 2018

Yau-Huei Wei

7

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15 May 2018

publication date

1 July 2007

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15 May 2018

Journal of the Formosan Medical Association

published in

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15 May 2018

volume

106

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15 May 2018

issue

7

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15 May 2018

page(s)

528-536

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15 May 2018

Approaches to the treatment of mitochondrial diseases

cites work

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https://api.crossref.org/works/10.1016%2FS0929-6646%2807%2960003-5

7 January 2021

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

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7 January 2021

Mitochondrial diseases in man and mouse

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7 January 2021

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

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https://api.crossref.org/works/10.1016%2FS0929-6646%2807%2960003-5

7 January 2021

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

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7 January 2021

Clinical spectrum of the MELAS mutation in a large pedigree.

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7 January 2021

Mitochondrial diseases

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7 January 2021

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

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7 January 2021

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

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7 January 2021

MELAS syndrome associated with a tandem duplication in the D-loop of mitochondrial DNA

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7 January 2021

A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy

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7 January 2021

MELAS: clinical features, biochemistry, and molecular genetics

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7 January 2021

Mitochondrial dysfunction and neuromuscular disease

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7 January 2021

Paralytic ileus in MELAS with phenotypic features of MNGIE.

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7 January 2021

Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes

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7 January 2021

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

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7 January 2021

A follow up study of myocardial involvement in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).

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7 January 2021

Clinical presentations of mitochondrial cardiomyopathies

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7 January 2021

Mitochondrial DNA and disease

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7 January 2021

Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.

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7 January 2021

Magnetic resonance imaging in MELAS syndrome

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7 January 2021

Serial imaging in MELAS.

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7 January 2021

Cerebral metabolism of oxygen and glucose in a patient with MELAS syndrome

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7 January 2021

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

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7 January 2021

Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes

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7 January 2021

MELAS- and kearns-sayre-type with myopathy and autoimmune polyendocrinopahy

1 reference

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7 January 2021

Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes

1 reference

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7 January 2021

A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers

1 reference

https://api.crossref.org/works/10.1016%2FS0929-6646%2807%2960003-5

7 January 2021

10.1016/S0929-6646(07)60003-5

Identifiers

DOI

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15 May 2018

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15 May 2018