Literature DB >> 506803

Amino acid metabolism in patients with a hereditary myopathy and paroxysmal myoglobinuria.

J Wahren, H Linderholm, P Felig.   

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Year:  1979        PMID： 506803     DOI： 10.1111/j.0954-6820.1979.tb13516.x

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN： 0001-6101


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  2 in total

1.  Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.

Authors:  U Drugge; M Holmberg; G Holmgren; B G Almay; H Linderholm
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

2.  Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.

Authors:  R G Haller; K G Henriksson; L Jorfeldt; E Hultman; R Wibom; K Sahlin; N H Areskog; M Gunder; K Ayyad; C G Blomqvist
Journal:  J Clin Invest       Date:  1991-10       Impact factor: 14.808
  2 in total

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