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4. Ultrastructure of skeletal muscle in muscular dystrophy, the carrier state and other human myopathies. Papadimitriou JM; Kakulas BA Proc Aust Assoc Neurol; 1968; 5(1):87-94. PubMed ID: 5250033 [No Abstract] [Full Text] [Related]
10. Electromyographic characteristics of congenital and early onset motor unit diseases. Fowler WM; Taylor RG; Munsat TL Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447 [No Abstract] [Full Text] [Related]
11. Recent contributions to the diagnosis of muscle disease. Zacks SI Hum Pathol; 1970 Sep; 1(3):465-98. PubMed ID: 4942055 [No Abstract] [Full Text] [Related]
12. [Clinically significant congenital myopathies]. Beckmann R Med Klin; 1974 Jul; 69(27):1175-84. PubMed ID: 4603414 [No Abstract] [Full Text] [Related]
13. Hypotonia in infancy. Dubowitz V Acta Univ Carol Med Monogr; 1976; (75):13-8. PubMed ID: 1077757 [No Abstract] [Full Text] [Related]
16. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage. Rose MR; Howard RS; Genet SA; McMahon CJ; Whitfield A; Morgan-Hughes JA Muscle Nerve; 1993 Jan; 16(1):57-62. PubMed ID: 8423832 [TBL] [Abstract][Full Text] [Related]
17. Muscle disorders in childhood. Dubowitz V Major Probl Clin Pediatr; 1978; 16():iii-xiii, 1-282. PubMed ID: 661378 [No Abstract] [Full Text] [Related]
18. Pathology of the muscular dystrophies and the congenital nonprogressive myopathies. Armbrustmacher VW Pathol Annu; 1980; 15(Pt 1):301-33. PubMed ID: 7443308 [No Abstract] [Full Text] [Related]
19. [Enzyme histochemistry in the biopsy diagnosis of skeletal muscle diseases]. Gullotta F Acta Histochem Suppl; 1983; 28():75-84. PubMed ID: 6412312 [TBL] [Abstract][Full Text] [Related]
20. The floppy infant syndrome in muscular glycogenosis. Zellweger H Padiatr Padol; 1972; 7(4):365-71. PubMed ID: 4263587 [No Abstract] [Full Text] [Related] [Next] [New Search]