(Q48590997)

13 February 2018

title

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1370535

19 September 2022

author name string

K. Inui

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1370535

19 September 2022

H. Fukushima

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1370535

19 September 2022

H. Tsukamoto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1370535

19 September 2022

M. Taniike

4

1 reference

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19 September 2022

M. Midorikawa

5

1 reference

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19 September 2022

J. Tanaka

6

1 reference

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19 September 2022

T. Nishigaki

7

1 reference

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19 September 2022

S. Okada

8

1 reference

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19 September 2022

language of work or name

English

0 references

publication date

1 January 1992

1 reference

13 February 2018

The Journal of Pediatrics

published in

1 reference

13 February 2018

volume

120

1 reference

13 February 2018

issue

1

1 reference

13 February 2018

page(s)

62-66

1 reference

13 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

7 January 2021

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

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%2FS0022-3476%2805%2980599-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Sequence and organization of the human mitochondrial genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Vascular involvement in mitochondrial myopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2980599-2

10.1016/S0022-3476(05)80599-2

7 January 2021

Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018