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22. [Spontaneous muscular activity of peripheral myotonic type in muscular dystrophy]. COLOMBI A Riv Sper Freniatr Med Leg Alien Ment; 1960 Dec; 84():1059-71. PubMed ID: 13694811 [No Abstract] [Full Text] [Related]
23. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Matsumura K; Campbell KP Muscle Nerve; 1994 Jan; 17(1):2-15. PubMed ID: 8264699 [TBL] [Abstract][Full Text] [Related]
24. Molecular diagnosis and modern management of Duchenne muscular dystrophy. Miller RG; Hoffman EP Neurol Clin; 1994 Nov; 12(4):699-725. PubMed ID: 7845338 [TBL] [Abstract][Full Text] [Related]
25. Molecular basis of neuromuscular diseases. Chance PF; Ashizawa T; Hoffman EP; Crawford TO Phys Med Rehabil Clin N Am; 1998 Feb; 9(1):49-81, vi. PubMed ID: 9894134 [TBL] [Abstract][Full Text] [Related]
26. [Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy]. Parnitzke C; Hagen EM Z Arztl Fortbild (Jena); 1981 Jul; 75(13):577-81. PubMed ID: 7314671 [No Abstract] [Full Text] [Related]
27. [Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy]. Wang X; Xie Y; Zhang C; Liu Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):239-42. PubMed ID: 12048687 [TBL] [Abstract][Full Text] [Related]
28. [The genetic basis of muscle disease]. Bindoff L; Gilhus NE Tidsskr Nor Laegeforen; 2003 Sep; 123(18):2588-92. PubMed ID: 14714051 [TBL] [Abstract][Full Text] [Related]
29. Congenital muscular dystrophies: New evidence-based guidelines for the diagnosis and management of this evolving group of muscle disorders. McMillan HJ Muscle Nerve; 2015 Jun; 51(6):791-2. PubMed ID: 25900129 [No Abstract] [Full Text] [Related]
30. [Therapy of muscular dystrophy]. MONCADA LORENZO E Rev Clin Esp; 1958 Jan; 68(2):113-5. PubMed ID: 13542929 [No Abstract] [Full Text] [Related]
32. [Update on diagnosis of limb girdle muscular dystrophy]. Nevo Y; Yaron Y Harefuah; 1999 May; 136(9):720-5. PubMed ID: 10955098 [No Abstract] [Full Text] [Related]
33. Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. Haliloglu G; Topaloglu H Neurology; 2015 Oct; 85(16):1432. PubMed ID: 26481930 [No Abstract] [Full Text] [Related]