(Q48847004)

16 February 2018

title

Resistance training in patients with single, large-scale deletions of mitochondrial DNA. (English)

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16 February 2018

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9

Tanja Taivassalo

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16 February 2018

2

Emma L Blakely

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16 February 2018

Robert William Taylor

7

Robert W Taylor

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16 February 2018

Douglass Matthew Turnbull

8

Douglass M Turnbull

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16 February 2018

Andrew M Schaefer

3

Andrew M Schaefer

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16 February 2018

Ronald G Hall

6

Ronald G Haller

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16 February 2018

Julie A Murphy

1

Julie L Murphy

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16 February 2018

author name string

Langping He

4

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16 February 2018

Phil Wyrick

5

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16 February 2018

language of work or name

English

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publication date

1 November 2008

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16 February 2018

published in

Brain

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16 February 2018

volume

131

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16 February 2018

issue

Pt 11

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16 February 2018

page(s)

2832-2840

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16 February 2018

Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy.

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Mitochondrial DNA deletion in "identical" twin brothers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Muscle fiber types: how many and what kind?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Reversal of a mitochondrial DNA defect in human skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Performance and physiologic adaptations to resistance training

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Cellular adaptation of the trapezius muscle in strength-trained athletes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Complete restoration of a wild-type mtDNA genotype in regenerating muscle fibres in a patient with a tRNA point mutation and mitochondrial encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Gene shifting: a novel therapy for mitochondrial myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

The diagnosis of mitochondrial muscle disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN252

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWN252

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16 February 2018

PubMed ID

18984605

1 reference

16 February 2018