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.
120 related articles for article (PubMed ID: 985151)
21. Axial computerized tomography of the brain in cases of early infantile spinal muscular atrophy (Werdnig-Hoffmann disease). Michałowicz R; Radelicka-Rajszys H; Krajewska G; Banaszek G; Szwabowska-Orzeszko E Mater Med Pol; 1985; 17(3):172-5. PubMed ID: 3831621 [No Abstract] [Full Text] [Related]
22. [Cases of familial Werdnig-Hoffmann syndrome, including a pair of concordant monozygotic twins (a case from the Eugenic Consultation Clinic)]. GEDDA L; DEL PORTO G; DEL PORTO-MERCURIA Acta Genet Med Gemellol (Roma); 1962 Apr; 11():113-23. PubMed ID: 13897442 [No Abstract] [Full Text] [Related]
34. The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England. Pearn JH J Med Genet; 1973 Sep; 10(3):260-5. PubMed ID: 4774536 [TBL] [Abstract][Full Text] [Related]
35. Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease. Pearn JH; Wilson J Arch Dis Child; 1973 Oct; 48(10):768-74. PubMed ID: 4749680 [TBL] [Abstract][Full Text] [Related]
36. [The muscle CT of the thigh in chronic Werdnig-Hoffmann disease]. Horikawa H; Konagaya M; Takayanagi T; Otsuji H Rinsho Shinkeigaku; 1986 May; 26(5):490-7. PubMed ID: 3742903 [No Abstract] [Full Text] [Related]