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.
5. Ultrastructure of chromatolytic motoneurons in a case of Werdnig-Hoffmann disease. Chou SM; Fakadej AV Neurology; 1970 Apr; 20(4):381. PubMed ID: 4104901 [No Abstract] [Full Text] [Related]
10. [Progressive infantile spinal atrophy. Werdnig-Hoffmann disease]. Sotelo-Cruz N; Torres-Cárdenas O; Gallegos-Gardner M Bol Med Hosp Infant Mex; 1984 Jul; 41(7):387-92. PubMed ID: 6477703 [No Abstract] [Full Text] [Related]
11. [XO-XY-sex-chromosomes-mosaicism in a child with progressive spinal muscular atrophy (author's transl)]. Kunze J; Tolksdorf M Z Kinderheilkd; 1973 Nov; 115(4):283-94. PubMed ID: 4778568 [No Abstract] [Full Text] [Related]
12. [Werdnigg-Hoffmann disease in the light of our personal observations]. Holendzki Z; Iwulska-Leśniowska M; Konert H Pediatr Pol; 1971 Mar; 46(3):338-44. PubMed ID: 5574207 [No Abstract] [Full Text] [Related]
13. [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]
14. [Clinical picture and genetics of Werdnig-Hoffman spinal amyotrophy in childhood]. Mazaeva IV Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1452-6. PubMed ID: 5139405 [No Abstract] [Full Text] [Related]
15. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children]. Olenev SN; Savel'eva-Vasil'eva ; Zav'ialova NS Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1445-9. PubMed ID: 4660417 [No Abstract] [Full Text] [Related]
16. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease). Fried K; Emery AE Clin Genet; 1971; 2(4):203-9. PubMed ID: 5146579 [No Abstract] [Full Text] [Related]
17. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies]. Bondarenko ES; Tamarkina AD; Zakoshchikova LV Vestn Akad Med Nauk SSSR; 1973; 28(7):38-44. PubMed ID: 4786657 [No Abstract] [Full Text] [Related]
18. [A genetic questionnaire. The genetic aspects of a case of benign spinal muscular dystrophy]. Klein D J Genet Hum; 1970 Dec; 18(4):421-2. PubMed ID: 5524821 [No Abstract] [Full Text] [Related]
19. [Variant of childhood spinal amyotrophy]. Savel'eva-Vasil'eva Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1456-61. PubMed ID: 5139406 [No Abstract] [Full Text] [Related]