(Q43615008)

25 November 2017

title

ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's disease (English)

1 reference

25 November 2017

main subject

mitochondrial disease

1 reference

Löfberg M

1

1 reference

25 November 2017

Lindholm H

2

1 reference

25 November 2017

Näveri H

3

1 reference

25 November 2017

Majander A

4

1 reference

25 November 2017

Suomalainen A

5

1 reference

25 November 2017

Paetau A

6

1 reference

25 November 2017

Sovijärvi A

7

1 reference

25 November 2017

Härkönen M

8

1 reference

25 November 2017

Somer H

9

1 reference

25 November 2017

publication date

1 May 2001

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25 November 2017

published in

Neuromuscular Disorders

1 reference

25 November 2017

volume

11

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25 November 2017

issue

4

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25 November 2017

page(s)

370-375

1 reference

Mitochondrial DNA and Disease

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Muscle metabolism during and after strenuous intermittent running

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Skeletal muscle lactate accumulation and creatine phosphate depletion during heavy exercise in congestive heart failure. Cause of limited exercise capacity?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Investigation of human mitochondrial myopathies by phosphorus magnetic resonance spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Bioenergetic heterogeneity of human mitochondrial myopathies: phosphorus magnetic resonance spectroscopy study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondrial disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Bioenergetics of skeletal muscle in mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

An autosomal locus predisposing to deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Metabolic causes of recurrent rhabdomyolysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Psychophysical bases of perceived exertion

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Direct measurement of high-energy phosphate compounds in patients with neuromuscular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Mitochondrial encephalomyopathy: correlation of P-31 exercise MR spectroscopy with clinical findings

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Contracture in McArdle's disease. Stability of adenosine triphosphate during contracture in phosphorylase-deficient human muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Examination of a case of suspected McArdle's syndrome by 31P nuclear magnetic resonance

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Muscle energy metabolism in McArdle's syndrome by in vivo phosphorus magnetic resonance spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Impairment of muscle mitochondrial oxidative metabolism in McArdle's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

31-P NMR characterization of the metabolic anomalies associated with the lack of glycogen phosphorylase activity in human forearm muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900205-4

7 January 2021

10.1016/S0960-8966(00)00205-4

Identifiers

DOI

1 reference

release_rzvduqfzofbvxp2acr7dtcsou4

25 November 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rzvduqfzofbvxp2acr7dtcsou4

24 November 2022

mapped directly with Wikidata item

1 reference