Maternally inherited Leigh syndrome. (Q52226853)

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scientific article published in March 1993

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Language	Label	Description	Also known as
English	Maternally inherited Leigh syndrome.	scientific article published in March 1993

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

title

Maternally inherited Leigh syndrome. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

author

Filippo Maria Santorelli

1 reference

stated in

ORCID Public Data File 2021

author name string

Ciafaloni E

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Santorelli FM

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Shanske S

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Deonna T

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Roulet E

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Janzer C

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

Pescia G

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

DiMauro S

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

language of work or name

English

0 references

publication date

1 March 1993

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

published in

The Journal of Pediatrics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

volume

122

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

page(s)

419-422

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

cites work

Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

X-linked Leigh's syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

MELAS: clinical features, biochemistry, and molecular genetics

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2983431-6

retrieved

7 January 2021

Identifiers

DOI

10.1016/S0022-3476(05)83431-6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

PubMed publication ID

8095070

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8095070

retrieved

27 April 2018

reference URL

http://europepmc.org/abstract/MED/8095070

 

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