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Journal Abstract Search
77 related items for PubMed ID: 5229456
1. McArdle's disease: three cases in an Australian family. Hammett JF, Bale P, Basser LS, Neale FC. Proc Aust Assoc Neurol; 1966; 4():21-5. PubMed ID: 5229456 [No Abstract] [Full Text] [Related]
3. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase. Rowland LP, Lovelace RE, Schotland DL, Araki S, Carmel P. Neurology; 1966 Jan; 16(1):93-100. PubMed ID: 5215287 [No Abstract] [Full Text] [Related]
8. McArdle's disease and anaesthesia: case reports. Review of potential problems and association with malignant hyperthermia. Bollig G, Mohr S, Raeder J. Acta Anaesthesiol Scand; 2005 Sep; 49(8):1077-83. PubMed ID: 16095447 [Abstract] [Full Text] [Related]
9. Histopathology of McArdle's disease in a family. Bale P, Hammett JF, Neale FC. J Pathol Bacteriol; 1967 Oct; 94(2):293-300. PubMed ID: 6066477 [No Abstract] [Full Text] [Related]
10. [Nation-wide survey on muscle glycogen storage disease (MGSDs) and comparison with our experiences in diagnosis of MGSDs]. Fukuda T, Sugie H, Ito M, Sugie Y, Saito K, Nishino I, Shimizu T. Rinsho Shinkeigaku; 2003 May; 43(5):243-8. PubMed ID: 12931628 [Abstract] [Full Text] [Related]
14. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene. Paradas C, Fernandez-Cadenas I, Gallardo E, Lligé D, Arenas J, Illa I, Andreu AL. Neurosci Lett; 2005 Dec 31; 391(1-2):28-31. PubMed ID: 16154688 [Abstract] [Full Text] [Related]