(Q51672440)

English

Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.

scientific article published in April 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

mitochondrial transfer

1 reference

based on heuristic

inferred from title

respiratory failure

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

Filippo Maria Santorelli

3

object named as

Filippo M Santorelli

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

author name string

Claudio Bruno

1

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Oliviero Sacco

2

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Stefania Assereto

4

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Emmanuel Tonoli

5

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Massimo Bado

6

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Giovanni A Rossi

7

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Carlo Minetti

8

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

publication date

1 April 2003

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Journal of Child Neurology

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

18

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

4

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

300-303

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

Does the patient have a mitochondrial encephalomyopathy?

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Mitochondria and the heart

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Mutations in mitochondrial DNA as a cause of exercise intolerance

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Mitochondrial DNA 8993 T > C mutation presenting as juvenile Leigh syndrome with respiratory failure.

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Quantitative amplification of genomic DNA from histological tissue sections after staining with nuclear dyes and laser capture microdissection

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Glycine tRNA mutants with normal anticodon loop size cause -1 frameshifting

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180040401

21 January 2018

Identifiers

10.1177/08830738030180040401

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/12760436

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