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Maximizing the Benefit of Life-Saving Treatments for Pompe Disease, Spinal Muscular Atrophy, and Duchenne Muscular Dystrophy Through Newborn Screening

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Year: 2019
Type: article
Source: JAMA Neurology
DOI: 10.1001/jamaneurol.2019.1206
Authors: Mei Baker, Robert Griggs, Barry Byrne, Anne M. Connolly, Richard Finkel, Lucja Grajkowska, Amanda Haidet-Phillips, Laura Hagerty, Robert Ostrander, Lianna Orlando, Kathryn Swoboda, Michael Watson, R. Rodney Howell
Institutions: University of Wisconsin–Madison, University of Rochester Medicine, University of Rochester, University of Florida, Washington University in St. Louis, Muscular Dystrophy Association, SUNY Upstate Medical University, Harvard University, Massachusetts General Hospital, American College of Medical Genetics, University of Miami
Language: English

Topic: Lysosomal Storage Disorders Research
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2945658923
FWCI: 2.228
Cites: 42
Cited by: 19
Related to: 10
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