Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria-Reference-Cited by-同舟云学术

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

Published:1990-07 Issue:1 Volume:228 Page:43-52
ISSN:0954-6820
Container-title:Journal of Internal Medicine
language:en
Short-container-title:

Author:

LINDERHOLM H.,ESSÉN-GUSTAVSSON B.,THORNELL L.-E.

Publisher

Wiley

Subject

Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2796.1990.tb00191.x/fullpdf

Reference32 articles.

1. Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis;Larsson;J Neurol Neurosurg Psychiatry,1964

2. Hereditary abnormal muscle metabolism with hyperkinetic circulation during exercise;Linderholm;Acta Med Scand,1969

3. Amino acid metabolism in patients with a hereditary myopathy and paroxysmal myoglobinuria;Wahren;Acta Med Scand,1979

4. Muscle electrolytes in man determined by neutron activation analysis on needle biopsy specimens: a study of normal subjects, kidney patients, and patients with chronic diarrhoea;Bergström;Scand J Clin Lab Invest,1962

5. Standard bicarbonate, its clinical significance, and a new method for its determination;Jörgensen;Scand J Clin Lab Invest,1957

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