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.
91 related articles for article (PubMed ID: 986033)
21. Myoglobinuria and skeletal muscle phosphorylase deficiency: report of a case of McArdle's disease. Nixon JC; Hobbs WK; Greenblatt J Can Med Assoc J; 1966 May; 94(19):977-85. PubMed ID: 4952390 [TBL] [Abstract][Full Text] [Related]
22. McArdle's disease--what limit to the age of onset? Hewlett RH; Gardner-Thorpe C S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990 [TBL] [Abstract][Full Text] [Related]
23. McArdle's disease: biochemical and molecular genetic studies. Servidei S; Shanske S; Zeviani M; Lebo R; Fletterick R; DiMauro S Ann Neurol; 1988 Dec; 24(6):774-81. PubMed ID: 3207360 [TBL] [Abstract][Full Text] [Related]
24. McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote. Schmidt B; Servidei S; Gabbai AA; Silva AC; de Sousa Bulle de Oliveira A; DiMauro S Neurology; 1987 Sep; 37(9):1558-61. PubMed ID: 3476861 [TBL] [Abstract][Full Text] [Related]
25. Myophosphorylase deficiency and limb-girdle muscular dystrophy in the same pedigree. Nishio T; Sunohara N; Nonaka I; Tsujino S; Sugie H Acta Neurol Scand; 1998 Nov; 98(5):364-7. PubMed ID: 9858109 [TBL] [Abstract][Full Text] [Related]
26. Ischemic exercise test: failure to detect partial expression of McArdle's disease. Taylor RG; Lieberman JS; Portwood MM Muscle Nerve; 1987; 10(6):546-51. PubMed ID: 3476851 [TBL] [Abstract][Full Text] [Related]
27. [Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review]. Mattle H; Jerusalem F Schweiz Med Wochenschr; 1977 Apr; 107(13):428-36. PubMed ID: 139680 [TBL] [Abstract][Full Text] [Related]
28. McArdle's disease heterozygotes. Metabolic adaptation assessed using 31P-nuclear magnetic resonance. Bogusky RT; Taylor RG; Anderson LJ; Angelos KL; Lieberman JS; Walsh DA J Clin Invest; 1986 Jun; 77(6):1881-7. PubMed ID: 3458722 [TBL] [Abstract][Full Text] [Related]
29. [A metabolic disease of muscles: the absence of phosphorylase (McArdle-Schmid-Pearson disease)]. SCHULLER E Presse Med (1893); 1962 Mar; 70():715-7. PubMed ID: 13909460 [No Abstract] [Full Text] [Related]
30. Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci. Tsujino S; Shanske S; Carroll JE; Sabina RL; DiMauro S Neuromuscul Disord; 1995 Jul; 5(4):263-6. PubMed ID: 7580237 [TBL] [Abstract][Full Text] [Related]