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4. Sporadic distal myopathy with early adult onset. Miller RG; Blank NK; Layzer RB Ann Neurol; 1979 Mar; 5(3):220-7. PubMed ID: 443754 [TBL] [Abstract][Full Text] [Related]
5. Quadriceps myopathy in two brothers: rare familial myopathy confirmed by muscle biopsy. Finelli PF R I Med J (1976); 1979 Apr; 62(4):125-9. PubMed ID: 286404 [No Abstract] [Full Text] [Related]
6. [Fundamentals and clinical significance of electromyography]. Buchthal F Verh Dtsch Ges Inn Med; 1965; 71():139-60. PubMed ID: 5877614 [No Abstract] [Full Text] [Related]
7. [Electromyography of myogenic diseases]. Dumoulin J; Clauses I; de Bisschop G Electrodiagn Ther; 1973; 10(4):117-32. PubMed ID: 4792176 [No Abstract] [Full Text] [Related]
8. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
9. Adult myopathy from glycogen storage disease due to acid maltase deficiency. Hudgson P; Gardner-Medwin D; Worsfold M; Pennington RJ; Walton JN Brain; 1968 Sep; 91(3):435-62. PubMed ID: 5247277 [No Abstract] [Full Text] [Related]
10. [Principles and significance of clinical electromyography]. Schmoigl S Wien Med Wochenschr; 1971 Mar; 121(13):250-5. PubMed ID: 5560230 [No Abstract] [Full Text] [Related]
11. 'Floppy baby' with normal mental and social responses. Case presentation. Goldie WD Hosp Pract (Off Ed); 1981 Nov; 16(11):37, 40-1. PubMed ID: 6797923 [No Abstract] [Full Text] [Related]
12. [Significance of electromyography and muscle biopsy in the diagnosis of neuromuscular diseases]. Murai Y; Ota M; Komoto K No To Shinkei; 1968 Jan; 20(1):19-25. PubMed ID: 5694858 [No Abstract] [Full Text] [Related]
13. Autosomal dominant centronuclear myopathy: report of a new family with clinical features simulating facioscapulohumeral syndrome. Felice KJ; Grunnet ML Muscle Nerve; 1997 Sep; 20(9):1194-6. PubMed ID: 9270681 [TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant late-onset quadriceps myopathy: three patients of a Taiwanese kindred. Chien YY; Nonaka I; Wang D Intern Med; 2011; 50(11):1175-81. PubMed ID: 21628932 [TBL] [Abstract][Full Text] [Related]
15. Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy with particular reference to the heterogeneity of Kugelberg-Welander disease. Furukawa T; Tsukagoshi H; Sugita H; Toyokura Y J Neurol Sci; 1969; 9(2):389-97. PubMed ID: 5345117 [No Abstract] [Full Text] [Related]
16. [Lipid storage myopathy--a contribution to the problem of the differential diagnosis of muscle dystrophy (Duchenne)]. Schmidt A; Hässler A Zentralbl Allg Pathol; 1983; 127(3-4):229-36. PubMed ID: 6880434 [TBL] [Abstract][Full Text] [Related]
17. The diagnostic significance of large action potentials in myopathy. Nakashima K; Tabuchi Y; Takahashi K J Neurol Sci; 1983 Oct; 61(2):161-70. PubMed ID: 6644325 [TBL] [Abstract][Full Text] [Related]
18. Electromyography in amyotrophic lateral sclerosis. A review. Marinacci AA; VonHagen KO Bull Los Angeles Neurol Soc; 1974 Jan; 39(1):17-29. PubMed ID: 4811862 [No Abstract] [Full Text] [Related]
19. Quantitative electromyography. IV. Correlative findings in motor unit bioelectric activity. Radu H Rev Roum Neurol; 1972; 9(1):19-22. PubMed ID: 5019764 [No Abstract] [Full Text] [Related]
20. [Electrodiagnosis and clinical picture of myopathies]. Huffmann G Z Allgemeinmed; 1974 Jan; 50(3):135-41. PubMed ID: 4826221 [No Abstract] [Full Text] [Related] [Next] [New Search]