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12. [Changes in glycogen metabolism in hereditary muscular diseases (review)]. Rozenfel'd EL Vopr Med Khim; 1986; 32(4):12-20. PubMed ID: 2945316 [TBL] [Abstract][Full Text] [Related]
13. Metabolic myopathies. DiMauro S; Miranda AF; Sakoda S; Schon EA; Servidei S; Shanske S; Zeviani M Am J Med Genet; 1986 Dec; 25(4):635-51. PubMed ID: 2878616 [TBL] [Abstract][Full Text] [Related]
14. Muscle glycogenosis. Dubowitz V Dev Med Child Neurol; 1966 Aug; 8(4):432-6. PubMed ID: 4226180 [No Abstract] [Full Text] [Related]
15. An electromyographic diagnostic screening test in McArdle's disease and a case report. Dyken ML; Smith DM; Peake RL Neurology; 1967 Jan; 17(1):45-50. PubMed ID: 4224654 [No Abstract] [Full Text] [Related]
16. [Myopathic form of phosphofructokinase deficiency]. Serratrice G; Monges A; Roux H; Aquaron R; Gambarelli D Rev Neurol (Paris); 1969 Apr; 120(4):271-7. PubMed ID: 4241954 [No Abstract] [Full Text] [Related]