Treatment algorithm for infants diagnosed with spinal muscular atrophy through newborn screening

Authors

Jacqueline Glascock, CureSMA
Jacinda Sampson, Stanford University
Amanda Haidet-Phillips, Muscular Dystrophy Assocation
Anne Connolly, Washington University School of Medicine in St. Louis
Basil Darras, Boston Children's Hospital
John Day, Stanford University
Richard Finkel, University of Central Florida
R. Rodney Howell, University of Miami
Katherine Klinger, Genzyme Corporation
Nancy Kuntz, Ann and Robert H. Lurie Children's Hospital of Chicago
Thomas Prior, Ohio State Wexner Medical Center
Perry B. Shieh, University of California, Los Angeles
Thomas O. Crawford, Johns Hopkins University
Douglas Ker, Generation Bio
Jill Jarecki, Cure SMA

Journal

Journal of Neuromuscular Diseases

Publication Date

2018

Volume

5

Issue

2

Inclusive Pages

145-158

Document Type

Open Access Publication

DOI

10.3233/JND-180304

Rights and Permissions

Glascock J, Sampson J, Haidet-Phillips A, et al (2018) Treatment algorithm for infants diagnosed with spinal muscular atrophy through newborn screening. Journal of Neuromuscular Diseases, 5(2):145-158. DOI: 10.3233/JND-180304 This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC 4.0).

Recommended Citation

Glascock, Jacqueline; Sampson, Jacinda; Haidet-Phillips, Amanda; Connolly, Anne; Darras, Basil; Day, John; Finkel, Richard; Howell, R. Rodney; Klinger, Katherine; Kuntz, Nancy; Prior, Thomas; Shieh, Perry B.; Crawford, Thomas O.; Ker, Douglas; and Jarecki, Jill, "Treatment algorithm for infants diagnosed with spinal muscular atrophy through newborn screening." Journal of Neuromuscular Diseases. 5, 2. 145-158. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/7460