175 related articles for article (PubMed ID: 1469240)
21. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
Spiegel R; Hagmann A; Boltshauser E; Moser H
Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311
[TBL] [Abstract][Full Text] [Related]
22. The genetics of the spinal muscular atrophies.
Baraitser M
Prog Clin Biol Res; 1989; 306():75-84. PubMed ID: 2662214
[No Abstract] [Full Text] [Related]
23. [Infantile spinal muscular atrophy].
Barois A; Estournet B; Duval-Beaupère G; Bataille J; Leclair-Richard D
Rev Neurol (Paris); 1989; 145(4):299-304. PubMed ID: 2660222
[TBL] [Abstract][Full Text] [Related]
24. The natural history of type I (severe) spinal muscular atrophy.
Thomas NH; Dubowitz V
Neuromuscul Disord; 1994; 4(5-6):497-502. PubMed ID: 7881295
[TBL] [Abstract][Full Text] [Related]
25. Muscle fatigue in spinal muscular atrophy.
Iannaccone ST; White M; Browne R; Russman B; Buncher R; Samaha FJ
J Child Neurol; 1997 Aug; 12(5):321-6. PubMed ID: 9378900
[TBL] [Abstract][Full Text] [Related]
26. Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot study.
Kirschner J; Schorling D; Hauschke D; Rensing-Zimmermann C; Wein U; Grieben U; Schottmann G; Schara U; Konrad K; Müller-Felber W; Thiele S; Wilichowski E; Hobbiebrunken E; Stettner GM; Korinthenberg R
Neuromuscul Disord; 2014 Feb; 24(2):134-42. PubMed ID: 24300782
[TBL] [Abstract][Full Text] [Related]
27. Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells.
Oates EC; Reddel S; Rodriguez ML; Gandolfo LC; Bahlo M; Hawke SH; Lamandé SR; Clarke NF; North KN
Brain; 2012 Jun; 135(Pt 6):1714-23. PubMed ID: 22628388
[TBL] [Abstract][Full Text] [Related]
28. A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN gene.
Lohkamp LN; von Au K; Goebel HH; Kress W; Grieben U; Drossel K; Garbes L; Wirth B; Heppner FL; Stenzel W
J Child Neurol; 2014 Feb; 29(2):254-9. PubMed ID: 24334346
[TBL] [Abstract][Full Text] [Related]
29. [Spinal muscular atrophy].
Porro G; Carboni P
Riv Neurol; 1988; 58(2):45-9. PubMed ID: 3051286
[No Abstract] [Full Text] [Related]
30. Spinal muscular atrophy.
Iannaccone ST
Semin Neurol; 1998; 18(1):19-26. PubMed ID: 9562664
[TBL] [Abstract][Full Text] [Related]
31. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
Haliloglu G; Chattopadhyay A; Skorodis L; Manzur A; Mercuri E; Talim B; Akçören Z; Renda Y; Muntoni F; Topaloğlu H
Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787
[TBL] [Abstract][Full Text] [Related]
32. Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3.
Wadman RI; Vrancken AF; van den Berg LH; van der Pol WL
Neurology; 2012 Nov; 79(20):2050-5. PubMed ID: 23115209
[TBL] [Abstract][Full Text] [Related]
33. Statistical considerations in the study of spinal muscular atrophy. Dallas-Cincinnati-Newington Spinal Muscular Atrophy (DCN-SMA) Study Group.
Buncher CR; Samaha F; Iannaccone ST; Russman BS; Cook JD; White M; McLaughlin C
Muscle Nerve; 1990; 13 Suppl():S45-8. PubMed ID: 2233886
[No Abstract] [Full Text] [Related]
34. Clinical characterizations of three adults with genetically confirmed spinal muscular atrophy: a case series.
Setyaningrum CTS; Harahap ISK; Nurputra DK; Ar Rochmah M; Sadewa AH; Alkarani GH; Harahap NIF
J Med Case Rep; 2022 Nov; 16(1):435. PubMed ID: 36376972
[TBL] [Abstract][Full Text] [Related]
35. Atrial Septal Defect, Neuromuscular Junction and Skeletal Abnormalities in Spinal Muscular Atrophy Type III.
Luan XH; Liu J
Chin Med J (Engl); 2017 Oct; 130(19):2382-2383. PubMed ID: 28937047
[No Abstract] [Full Text] [Related]
36. [Two cases of Werdnig-Hofmann disease].
Palmer-Morales Y; Pacheco-Flores G; Ames-Guevara Y; Gaxiola-Apodaca M; Gaspar-Franco D; Landavazo-Acuña G; Hernández-Rocha F
Rev Med Inst Mex Seguro Soc; 2010; 48(3):317-9. PubMed ID: 21192906
[TBL] [Abstract][Full Text] [Related]
37. Managing pregnancy in a spinal muscular atrophy type III patient in Indonesia: a case report.
Setyaningrum CTS; Harahap ISK; Nurputra DK; Rachman IT; Harahap NIF
J Med Case Rep; 2022 Jan; 16(1):14. PubMed ID: 35033190
[TBL] [Abstract][Full Text] [Related]
38. Spinal muscular atrophy.
Wessel HB
Pediatr Ann; 1989 Jul; 18(7):421-7. PubMed ID: 2666923
[No Abstract] [Full Text] [Related]
39. Clinical characteristics of three subtypes of spinal muscular atrophy in children.
Yuan P; Jiang L
Brain Dev; 2015 May; 37(5):537-41. PubMed ID: 25199871
[TBL] [Abstract][Full Text] [Related]
40. Electrocardiographic findings in children with spinal muscular atrophy.
Huang JJ; Jong YJ; Huang MY; Chiang CH; Huang TY
Jpn Heart J; 1996 Mar; 37(2):239-42. PubMed ID: 8676550
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
