Disease burden of spinal muscular atrophy in Germany-Reference-Cited by-同舟云学术

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Disease burden of spinal muscular atrophy in Germany

Published:2016-05-04 Issue:1 Volume:11 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Klug Constanze,Schreiber-Katz Olivia,Thiele Simone,Schorling Elisabeth,Zowe Janet,Reilich Peter,Walter Maggie C.,Nagels Klaus H.

Funder

Friedrich-Baur-GmbH

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-016-0424-0

Reference38 articles.

1. Kolb SJ, Kissel JT. Spinal Muscular Atrophy. Neurol Clin. 2015;33(4):831–46. doi: 10.1016/j.ncl.2015.07.004 .

2. Darras BT. Spinal muscular atrophies. Pediatr Clin North Am. 2015;62(3):743–66. doi: 10.1016/j.pcl.2015.03.010 .

3. Lefebvre S, Burglen L, Reboullet S, Clermont O, Burlet P, Viollet L, et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 1995;80(1):155–65.

4. D’Amico A, Mercuri E, Tiziano FD, Bertini E. Spinal muscular atrophy. Orphanet J Rare Dis. 2011;6(1):71. doi: 10.1186/1750-1172-6-71 .

5. Wang CH, Finkel RS, Bertini ES, Schroth M, Simonds A, Wong B, et al. Consensus statement for standard of care in spinal muscular atrophy. J Child Neurol. 2007;22(8):1027–49. doi: 10.1177/0883073807305788 .

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