(Q48383509)

11 February 2018

title

The brain-heart connection in mitochondrial respiratory chain diseases (English)

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11 February 2018

M Grazina

5

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author name string

M Cordeiro

1

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11 February 2018

F Scaglia

2

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11 February 2018

S Lopes Da Silva

3

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11 February 2018

P Garcia

4

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C Moura

6

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L Diogol

7

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11 February 2018

publication date

14 December 2009

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11 February 2018

The Neuroradiology Journal

published in

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11 February 2018

volume

22

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11 February 2018

issue

5

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11 February 2018

page(s)

558-563

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11 February 2018

Developing a systematic approach to the diagnosis and classification of mitochondrial disease

cites work

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Diagnostic criteria for respiratory chain disorders in adults and children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Infantile leukoencephalopathy owing to mitochondrial enzyme dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Pediatric mitochondrial respiratory chain disorders in the Centro region of Portugal

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Neurocardiology. An interdisciplinary area for the 80s.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

The brain-heart connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

Destruction of neurons in the VPM thalamus prevents rabbit heart rate conditioning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F197140090902200508

10.1177/197140090902200508

21 January 2018

Identifiers

DOI

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11 February 2018

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11 February 2018