These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Biochemical determinations in a recently investigated case of McArdle's disease. Luca N, Bănileanu S. Eur Neurol; 1974 Jun; 11(1):58-68. PubMed ID: 4524323 [No Abstract] [Full Text] [Related]
3. [Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)]. Delwaide PJ, Reznik M, Lemaire R, Lelièvre P, Bonnet F. Rev Neurol (Paris); 1967 Feb; 116(2):119-40. PubMed ID: 5230980 [No Abstract] [Full Text] [Related]
4. McArdle's myopathy. A report of a case with observations on the muscle ultrastructure. Brownell B, Hughes JT, Goldby FS, Woods HF. J Neurol Sci; 1969 Feb; 9(3):515-26. PubMed ID: 5367042 [No Abstract] [Full Text] [Related]
5. [McArdle's metabolic myopathy]. Shutov AA, Bessonov AV, Sidorov VV. Zh Nevropatol Psikhiatr Im S S Korsakova; 1974 Feb; 74(10):1485-90. PubMed ID: 4530582 [No Abstract] [Full Text] [Related]
6. McArdle's syndrome (myophosphorylase deficiency). A study of a family. Salter RH, Adamson DG, Pearce GW. Q J Med; 1967 Oct; 36(144):565-78. PubMed ID: 5235736 [No Abstract] [Full Text] [Related]
7. Glucose arteriovenous differences across muscle in McArdle's disease. Turner CE, Waterhouse C. Am J Med Sci; 1973 Feb; 265(2):109-15. PubMed ID: 4513596 [No Abstract] [Full Text] [Related]