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10. [Ultrastructural findings and characterization of isoenzymes in the muscle in case of Werdnig-Hoffmann disease]. Ferreli A; Cao A; Onnis C Arch De Vecchi Anat Patol; 1967 Dec; 50(3):629-44. PubMed ID: 5634345 [No Abstract] [Full Text] [Related]
11. [Infantile neurogenic amyotrophies with prolonged course: the problem of their nosologic classification in relation to Werdnig-Hoffmann's disease]. Lugaresi E; Giovanardi-Rossi P; Gambetti P Riv Sper Freniatr Med Leg Alien Ment; 1965 Jun; 89(3):594-619. PubMed ID: 5845541 [No Abstract] [Full Text] [Related]
12. Pathological findings in Werdnig-Hoffmann's disease with special remarks on diencephalic lesions. Nieves GM; Castello JC Eur Neurol; 1970; 3(4):231-40. PubMed ID: 5435261 [No Abstract] [Full Text] [Related]
13. Werdnig-Hoffmann disease with congenital hypothyroidism. Gunes T; Akcakus M; Cetin N; Kurtoğlu S; Kumandaş S Ann Trop Paediatr; 2003 Dec; 23(4):301-4. PubMed ID: 14738578 [TBL] [Abstract][Full Text] [Related]
14. Neuronal RNA metabolism in infantile spinal muscular atrophy (Werdnig-Hoffmann's disease) studied by radioautography: a new technic in the investigation of neurological disease. Hogenhuis LA; Spaulding SW; Engel WK J Neuropathol Exp Neurol; 1967 Apr; 26(2):335-41. PubMed ID: 6022173 [No Abstract] [Full Text] [Related]
15. A case of congenital Werdnig-Hoffmann disease with glial bundles in spinal roots. Mitsumoto H; Adelman LS; Liu HC Ann Neurol; 1982 Feb; 11(2):214-6. PubMed ID: 7073257 [No Abstract] [Full Text] [Related]