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.
4. Biochemistry of striated muscle during human muscular diseases. Schapira G; Dreyfus JC; Schapira F Enzymol Biol Clin (Basel); 1970; 11(1):8-31. PubMed ID: 4905517 [No Abstract] [Full Text] [Related]
5. The diagnostic quagmire of muscle diseases in adulthood. Klinkerfuss GH Geriatrics; 1975 Feb; 30(2):135-7, 141-3. PubMed ID: 1054667 [No Abstract] [Full Text] [Related]
6. [Spinal muscular atrophy with features of myasthenia gravis and Eaton-Lambert syndrome. A case report]. Ono S; Kurisaki H Rinsho Shinkeigaku; 1988 May; 28(5):497-500. PubMed ID: 2850884 [No Abstract] [Full Text] [Related]
11. 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]
12. [Waning and waxing phenomena in neuromuscular diseases in children]. Segawa M; Nihei K; Aoyama M Shinkei Kenkyu No Shimpo; 1970; 14(3):527-32. PubMed ID: 4250543 [No Abstract] [Full Text] [Related]
14. [Diagnostic problems in various types of glycogenosis]. Tulzer W; Ploier R; Klatt R Wien Med Wochenschr; 1974 Jun; 124(25):428-31. PubMed ID: 4525974 [No Abstract] [Full Text] [Related]
19. Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and V. DiMauro S; Rowland LP; Mellman WJ Pediatr Res; 1973 Sep; 7(9):739-44. PubMed ID: 4200717 [No Abstract] [Full Text] [Related]