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29. [Myopathy in a 19-year old girl diagnosed post mortem as glycogenosis]. Fidziańska A; Hausmanowa-Petrusewicz I Neuropatol Pol; 1968; 6(3):305-16. PubMed ID: 5247043 [No Abstract] [Full Text] [Related]
30. [Congenital and metabolic myopathies]. Kinoshita M No To Hattatsu; 1983; 15(2):105-12. PubMed ID: 6573882 [No Abstract] [Full Text] [Related]
32. [Glycogen storage disease caused by absence of amylo-1,6-glucosidase. Hepatomuscular and isolated hepatic forms]. CHAPTAL J; JEAN R; CRASTES DE PAULE ; GUILLAUMOT R; MOREL G Arch Ital Pediatr Pueric; 1962 Nov; 22():161-77. PubMed ID: 14020187 [No Abstract] [Full Text] [Related]
33. Proglycogen, macroglycogen, glucose, and glucose-6-phosphate concentrations in skeletal muscles of horses with polysaccharide storage myopathy performing light exercise. Bröjer JT; Essén-Gustavsson B; Annandale EJ; Valberg SJ Am J Vet Res; 2006 Sep; 67(9):1589-94. PubMed ID: 16948606 [TBL] [Abstract][Full Text] [Related]
34. [Myasthenic form of a metabolic myopathy with dystrophic changes due to storage and symptoms resembling McArdle's syndrome (a case report)]. Wagner A; Zett W Psychiatr Neurol Med Psychol (Leipz); 1971 Nov; 23(11):650-7. PubMed ID: 5291479 [No Abstract] [Full Text] [Related]
35. Laboratory diagnosis of the neuromuscular glycogen storage diseases. Farmer PM Ann Clin Lab Sci; 1982; 12(6):431-8. PubMed ID: 6817693 [TBL] [Abstract][Full Text] [Related]
39. [Myopathy caused by acid maltase deficiency in an adult]. Cartier L; Cea JG; Slachevsky A Rev Med Chil; 1995 Jun; 123(6):758-61. PubMed ID: 8525231 [TBL] [Abstract][Full Text] [Related]