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.
111 related articles for article (PubMed ID: 1552561)
21. Two cases of neonatal muscular atrophy: nosological problems. Martini ME; Stella F; Santacroce C Birth Defects Orig Artic Ser; 1996; 30(1):359-68. PubMed ID: 9125341 [No Abstract] [Full Text] [Related]
22. Brain atrophy in Werdnig-Hoffmann disease. Yohannan M; Patel P; Kolawole T; Malabarey T; Mahdi A Acta Neurol Scand; 1991 Nov; 84(5):426-8. PubMed ID: 1776391 [TBL] [Abstract][Full Text] [Related]
23. Selective type II muscle fiber hypertrophy in severe infantile spinal muscular atrophy. Kingma DW; Feeback DL; Marks WA; Bobele GB; Leech RW; Brumback RA J Child Neurol; 1991 Oct; 6(4):329-34. PubMed ID: 1940135 [TBL] [Abstract][Full Text] [Related]
24. [Unusual complications at birth in a stillborn with spinal muscular atrophy]. Lüders H; Meerbach W; Grauel BM Zentralbl Allg Pathol; 1988; 134(6):567-74. PubMed ID: 3213291 [TBL] [Abstract][Full Text] [Related]
25. [Anatomoclinical correlations of spinal muscular atrophy in infancy]. Rufo Campos M; Chinchón Lara I; Arias León E; Martínez López A; Gómez de Terreros I Neurologia; 1993 Mar; 8(3):105-9. PubMed ID: 8448040 [TBL] [Abstract][Full Text] [Related]
26. Digital necroses and vascular thrombosis in severe spinal muscular atrophy. Rudnik-Schöneborn S; Vogelgesang S; Armbrust S; Graul-Neumann L; Fusch C; Zerres K Muscle Nerve; 2010 Jul; 42(1):144-7. PubMed ID: 20583119 [TBL] [Abstract][Full Text] [Related]
27. Congenital caudal spinal atrophy: a case report. Tsukamoto H; Inagaki M; Tomita Y; Ohno K Neuropediatrics; 1992 Oct; 23(5):260-2. PubMed ID: 1454146 [TBL] [Abstract][Full Text] [Related]
28. Lumbosacral ventral spinal nerve root atrophy identified on MRI in a case of spinal muscular atrophy type II. Smith G; Bell SK; Sladky JT; Kang PB; Albayram MS Clin Imaging; 2019; 53():134-137. PubMed ID: 30340076 [TBL] [Abstract][Full Text] [Related]
32. Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene-disease relationship. Lu W; Liang M; Su J; Wang J; Li L; Zhang S; Qin Z; Huang L; Lu Y; Yi S; Yi S; Xie B; Zheng H; Luo J; Gao X; Shen Y Mol Genet Genomic Med; 2020 May; 8(5):e1212. PubMed ID: 32160656 [TBL] [Abstract][Full Text] [Related]
33. [Type I spinal muscular atrophy in twins]. Rufo Campos M; Arias León E; Martínez López A; Chinchón Lara I; Gómez de Terreros I An Esp Pediatr; 1993 Jun; 38(6):557-8. PubMed ID: 8368689 [No Abstract] [Full Text] [Related]
34. [Enzyme-and immuno-histochemistry of muscle biopsies in severe infantile spinal muscular atrophy]. Chen BF Zhonghua Bing Li Xue Za Zhi; 1991 Mar; 20(1):38-40. PubMed ID: 2065375 [TBL] [Abstract][Full Text] [Related]
36. Infantile spinal muscular atrophy - the potential for cure of a fatal disease. Volpe JJ J Neonatal Perinatal Med; 2021; 14(2):153-157. PubMed ID: 33459670 [No Abstract] [Full Text] [Related]
37. Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1). Rudnik-Schöneborn S; Stolz P; Varon R; Grohmann K; Schächtele M; Ketelsen UP; Stavrou D; Kurz H; Hübner C; Zerres K Neuropediatrics; 2004 Jun; 35(3):174-82. PubMed ID: 15248100 [TBL] [Abstract][Full Text] [Related]
38. Mutation of gene in spinal muscular atrophy respiratory distress type I. Wong VC; Chung BH; Li S; Goh W; Lee SL Pediatr Neurol; 2006 Jun; 34(6):474-7. PubMed ID: 16765827 [TBL] [Abstract][Full Text] [Related]
39. 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]