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Journal Abstract Search
149 related items for PubMed ID: 4738322
21. 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]
22. [Werding-Hoffmann disease and Kugelberg-Welander disease]. Uono M. No To Shinkei; 1970 Aug; 22(8):902-6. PubMed ID: 5468436 [No Abstract] [Full Text] [Related]
23. Spinal muscular atrophy. McLeod JG, Williams IM. Minn Med; 1971 Jun; 54(6):457-61. PubMed ID: 5559368 [No Abstract] [Full Text] [Related]
24. [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 Jun; 41(3):196-217. PubMed ID: 5126436 [No Abstract] [Full Text] [Related]
25. [Benign familial proximal amyotrophy with late onset (presentation of a case with dominant hereditary transmission)]. Cianchetti C, Tonato M, Signorini E. Riv Patol Nerv Ment; 1969 Dec; 90(6):481-92. PubMed ID: 5406113 [No Abstract] [Full Text] [Related]
34. [Family with progressive myelopathic muscular atrophy with proximal distribution and onset in adulthood]. Mapelli G. Riv Patol Nerv Ment; 1983 Mar 31; 104(4):159-70. PubMed ID: 6681331 [Abstract] [Full Text] [Related]
35. Sex-linked form of Kugelberg-Welander syndrome. Paulson GW, Liss L, Sweeney PJ. Trans Am Neurol Assoc; 1977 Mar 31; 102():177-9. PubMed ID: 616104 [No Abstract] [Full Text] [Related]
37. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)]. Fujimori N, Hanyu N, Oguchi K, Yanagisawa N, Tsukagoshi H. Rinsho Shinkeigaku; 1980 Jun 31; 20(6):423-9. PubMed ID: 7408341 [No Abstract] [Full Text] [Related]
38. [XO-XY-sex-chromosomes-mosaicism in a child with progressive spinal muscular atrophy (author's transl)]. Kunze J, Tolksdorf M. Z Kinderheilkd; 1973 Nov 19; 115(4):283-94. PubMed ID: 4778568 [No Abstract] [Full Text] [Related]