ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle’s disease-Reference-Cited by-同舟云学术

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ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle’s disease

Published:2001-05 Issue:4 Volume:11 Page:370-375
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Löfberg Mervi,Lindholm Harri,Näveri Hannu,Majander Anna,Suomalainen Anu,Paetau Anders,Sovijärvi Anssi,Härkönen Matti,Somer Hannu

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference23 articles.

1. Mitochondrial DNA and disease;Suomalainen;Ann Med,1997

2. Muscle metabolism during and after strenuous intermittent running;Näveri;Scand J Clin Lab Invest,1978

3. Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria;Linderholm;J Intern Med,1990

4. Skeletal muscle lactate accumulation and creatine phosphate depletion during heavy exercise in congestive heart failure. Cause of limited exercise capacity?;Näveri;Eur Heart J,1997

5. Investigation of human mitochondrial myopathies by phosphorus magnetic resonance spectroscopy;Arnold;Ann Neurol,1985

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2. 3D localized lactate detection in muscle tissue using double‐quantum filtered 1 H MRS with adiabatic refocusing pulses at 7 T;Magnetic Resonance in Medicine;2021-10-31

3. Exercise Testing, Physical Training and Fatigue in Patients with Mitochondrial Myopathy Related to mtDNA Mutations;Journal of Clinical Medicine;2021-04-20

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5. Exercise responses in patients with chronically high creatine kinase levels;Muscle & Nerve;2017-03-29

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