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5. [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]
7. [A case of Werdnig-Hoffmann disease in a newborn infant]. Guarniere J; Inferrera C; Di Prima C; Barresi G Pediatria (Napoli); 1977 Dec; 85(4):625-44. PubMed ID: 349495 [No Abstract] [Full Text] [Related]
8. Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease. Hausmanowa-Petrusewicz I; Fidzianska A Bull N Y Acad Med; 1974 Dec; 50(11):1157-72. PubMed ID: 4529631 [No Abstract] [Full Text] [Related]
9. [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]
10. [Infantile progressive spinal muscular atrophy. Werdnig-Hoffmann disease]. Mohr W; Olischläger A; Carl H Med Welt; 1971 Aug; 35():1317-9. PubMed ID: 5564452 [No Abstract] [Full Text] [Related]
11. 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]
18. [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]
19. Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease. Goebel HH; Zeman W; DeMyer W Neuropadiatrie; 1976 May; 7(2):182-95. PubMed ID: 183171 [TBL] [Abstract][Full Text] [Related]
20. [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]. Drac H Neuropatol Pol; 1977; 15(1):1-16. PubMed ID: 840382 [No Abstract] [Full Text] [Related] [Next] [New Search]