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.
137 related articles for article (PubMed ID: 4646546)
1. A new genetic variant of the spinal muscular atrophies in infancy. Zellweger H; Hanhart E; Schneider HJ J Med Genet; 1972 Dec; 9(4):401-7. PubMed ID: 4646546 [No Abstract] [Full Text] [Related]
2. Electromyographic studies in parents of children with spinal muscular atrophy. Emery AE; Anderson AR; Noronha MJ J Med Genet; 1973 Mar; 10(1):8-10. PubMed ID: 4697860 [TBL] [Abstract][Full Text] [Related]
3. The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England. Pearn JH J Med Genet; 1973 Sep; 10(3):260-5. PubMed ID: 4774536 [TBL] [Abstract][Full Text] [Related]
4. An unusual inheritane pattern for spinal muscular atrophy. White NR; Blaw ME Dev Med Child Neurol; 1971 Oct; 13(5):621-4. PubMed ID: 5119919 [No Abstract] [Full Text] [Related]
5. 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]
6. Spinal muscular atrophy. McLeod JG; Williams IM Minn Med; 1971 Jun; 54(6):457-61. PubMed ID: 5559368 [No Abstract] [Full Text] [Related]
7. The nosology of the spinal muscular atrophies. Emery AE J Med Genet; 1971 Dec; 8(4):481-95. PubMed ID: 4948374 [No Abstract] [Full Text] [Related]
8. [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]
9. [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]
10. [Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies]. Tangheroni W; Cao A; Cianchetti C; Calisti L Minerva Pediatr; 1974 Jun; 26(22):1125-45. PubMed ID: 4276719 [No Abstract] [Full Text] [Related]
12. Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases. Ghetti B; Amati A; Turra MV; Pacini A; Del Vecchio M; Guazzi GC Acta Genet Med Gemellol (Roma); 1971 Jan; 20(1):43-58. PubMed ID: 5568110 [No Abstract] [Full Text] [Related]
13. [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]
14. [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]
15. Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease. Pearn JH; Wilson J Arch Dis Child; 1973 Oct; 48(10):768-74. PubMed ID: 4749680 [TBL] [Abstract][Full Text] [Related]
16. Inherited spinal muscular atrophies. Kerr C Minn Med; 1971 Jun; 54(6):429-30. PubMed ID: 5559364 [No Abstract] [Full Text] [Related]
17. [Haptoglobins in muscular diseases]. Rosnowska M; Strugalska H Neurol Neurochir Pol; 1970; 4(6):655-60. PubMed ID: 5487716 [No Abstract] [Full Text] [Related]