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10. [Werdnig-Hoffmann spinal amyotrophy in twins]. Mazaeva IV; Lipovetskaia NG; Balashova EG Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(10):1491-5. PubMed ID: 4795172 [No Abstract] [Full Text] [Related]
11. Intrafamilial variability in spinal muscular atrophy. Prot J; Sawicka E Pol Med J; 1969; 8(5):1165-9. PubMed ID: 5383931 [No Abstract] [Full Text] [Related]
12. High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel. Fried K; Mundel G Clin Genet; 1977 Oct; 12(4):250-1. PubMed ID: 912942 [TBL] [Abstract][Full Text] [Related]
13. Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings. Tolksdorf M; Kunze J; Gross-Selbeck G; Sperling K; Wegner RD; Wieczorek V; Vogel M Eur J Pediatr; 1977 Aug; 126(1-2):13-27. PubMed ID: 902660 [TBL] [Abstract][Full Text] [Related]
14. Werdnig-Hoffmann disease: proposal of a pathogenetic mechanism. Chou SM; Nonaka I Acta Neuropathol; 1978 Jan; 41(1):45-54. PubMed ID: 636837 [TBL] [Abstract][Full Text] [Related]
15. A new genetic variant of spinal muscular atrophy. Zellweger H; Schneider H; Schuldt DR Neurology; 1969 Sep; 19(9):865-9. PubMed ID: 5816880 [No Abstract] [Full Text] [Related]
16. Cerebellar hypoplasia in Werdnig-Hoffmann disease. Weinberg AG; Kirkpatrick JB Dev Med Child Neurol; 1975 Aug; 17(4):511-6. PubMed ID: 1158057 [TBL] [Abstract][Full Text] [Related]