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26. Transmission block in terminal nerve twigs: a single fibre electromyographic finding in man. Stålberg E; Thiele B J Neurol Neurosurg Psychiatry; 1972 Feb; 35(1):52-9. PubMed ID: 4337272 [TBL] [Abstract][Full Text] [Related]
27. Oculopharyngeal involvement in familial neurogenic muscular atrophy. Matsunaga M; Inokuchi T; Onishi A; Kuroiwa Y J Neurol Neurosurg Psychiatry; 1973 Feb; 36(1):104-11. PubMed ID: 4691681 [TBL] [Abstract][Full Text] [Related]
28. Dissociated small hand muscle atrophy in amyotrophic lateral sclerosis: frequency, extent, and specificity. Kuwabara S; Sonoo M; Komori T; Shimizu T; Hirashima F; Inaba A; Misawa S; Hatanaka Y; Muscle Nerve; 2008 Apr; 37(4):426-30. PubMed ID: 18236469 [TBL] [Abstract][Full Text] [Related]
29. [Utilization of a universal computer of impulses during electromyographic examination of progressive muscular dystrophy and amyotrophic lateral sclerosis]. Sercl M; Kyral V; Dusek V; Lichý J; Kovarík J Cesk Neurol; 1970 Jan; 33(1):12-9. PubMed ID: 5412258 [No Abstract] [Full Text] [Related]
30. Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: evidence of activity-dependent conduction block. Noto Y; Misawa S; Mori M; Kawaguchi N; Kanai K; Shibuya K; Isose S; Nasu S; Sekiguchi Y; Beppu M; Ohmori S; Nakagawa M; Kuwabara S Clin Neurophysiol; 2013 Sep; 124(9):1893-8. PubMed ID: 23643309 [TBL] [Abstract][Full Text] [Related]
31. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy]. Raimbault J; Laget P Pathol Biol (Paris); 1972 Mar; 20(5):287-96. PubMed ID: 4556213 [No Abstract] [Full Text] [Related]
33. Electromyographic studies in parents of children with spinal muscular atrophy. Emery AE; Anderson AR; Noronha MJ J Med Genet; 1973 Mar; 10(1):8-10. PubMed ID: 4697860 [TBL] [Abstract][Full Text] [Related]
34. Electromyography and nerve conduction measurements. Nagler W Am Fam Physician; 1974 Sep; 10(3):89-97. PubMed ID: 4369979 [No Abstract] [Full Text] [Related]
35. Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases. Ghetti B; Amati A; Turra MV; Pacini A; Del Vecchio M; Guazzi GC Acta Genet Med Gemellol (Roma); 1971 Jan; 20(1):43-58. PubMed ID: 5568110 [No Abstract] [Full Text] [Related]
36. [Hereditary proximal neurogenic muscular atrophy (Wohlfart-Kugelberg-Welander disease). Electromyographic, anatomo-pathologic and clinical study in 3 brothers]. De Freitas MR; Nascimento OJ Arq Neuropsiquiatr; 1976 Mar; 34(1):81-8. PubMed ID: 1259636 [TBL] [Abstract][Full Text] [Related]
37. Fibre density, amplitudes of macro-EMG motor unit potentials and conventional EMG recordings from the anterior tibial muscle in patients with amyotrophic lateral sclerosis. A study on 51 cases. Tackmann W; Vogel P J Neurol; 1988 Jan; 235(3):149-54. PubMed ID: 3367162 [TBL] [Abstract][Full Text] [Related]
38. Fasciculation discharge frequency in amyotrophic lateral sclerosis and related disorders. de Carvalho M; Swash M Clin Neurophysiol; 2016 May; 127(5):2257-62. PubMed ID: 27072098 [TBL] [Abstract][Full Text] [Related]
40. [Observations on a case of amyotrophic lateral sclerosis and 2 cases of infantile spina proximal amyotrophy in the same family]. Tonali P; Anepeta L Riv Neurol; 1971; 41(3):196-217. PubMed ID: 5126436 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]