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2. [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children]. BRANDT S Nord Med; 1950 Sep; 44(37):1499. PubMed ID: 14806955 [No Abstract] [Full Text] [Related]
3. Werdnig-Hoffmann's disease. Warpus JM ONA J; 1979 Jul; 6(7):287-9. PubMed ID: 257292 [No Abstract] [Full Text] [Related]
4. Werdnig-Hoffmann's progressive muscular atrophy. Creatine excretion following vitamin E treatment and muscle radiography. FRANTZELL A; HAGBERG B; SODERHJELM L Acta Soc Med Ups; 1951; 56(5-6):209-23. PubMed ID: 14902615 [No Abstract] [Full Text] [Related]
5. [Two cases of a proximal spinal muscular atrophy (Werdnig-Hoffmann's disease) in one family]. Nurbekova UA Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(10):106-7. PubMed ID: 25591528 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. [On the morphology, nosological position and pathogenesis of Oppenheim's myotonia congenita and Werdnig-Hoffmann's infantile spinal progressive muscular atrophy]. GEILER G; GEILER G Virchows Arch Pathol Anat Physiol Klin Med; 1962; 335():654-67. PubMed ID: 13897523 [No Abstract] [Full Text] [Related]
11. [Studies on Werdnig-Hoffmann's disease. 3. Anatomo-pathological and histochemical contribution]. Mercante G; Crosta C Riv Anat Patol Oncol; 1967; 30(2):115-47. PubMed ID: 5608996 [No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. [Course in infantile progressive spinal muscle atrophy of the Werdnig-Hoffmann and Oppenheim types]. ZEIDLER U Z Kinderheilkd; 1958; 81(3):315-29. PubMed ID: 13604560 [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]
17. [Spinal amyotonia-amyotrophy (Werdnig-Hoffman disease) on the basis of observation of 40 cases]. Lesný I; Kocura P; Jirásek A; Krahulec B Cesk Neurol Neurochir; 1980 Jan; 43(1):26-31. PubMed ID: 7357655 [No Abstract] [Full Text] [Related]
18. Spinal muscular atrophy with respiratory distress type 1 (SMARD1). Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757 [TBL] [Abstract][Full Text] [Related]
19. Early diagnosis and treatment reverse clinical features in Hoffmann's syndrome due to hypothyroid myophaty: a case report. Ozdag MF; Eroglu E; Ulas UH; Ipekdal I; Odabasi Z; Vural O Acta Neurol Belg; 2005 Dec; 105(4):212-3. PubMed ID: 16482871 [TBL] [Abstract][Full Text] [Related]
20. Two Cases of Amyotonia Congenita (Werdnig-Hoffmann's Disease). Bolton M Proc R Soc Med; 1933 Dec; 27(2):120-1. PubMed ID: 19989564 [No Abstract] [Full Text] [Related] [Next] [New Search]