Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal
Authors
Keywords
-
Journal
MUSCLE & NERVE
Volume 54, Issue 2, Pages 186-191
Publisher
Wiley
Online
2016-05-12
DOI
10.1002/mus.25185
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy
- (2016) Jerry R. Mendell et al. ANNALS OF NEUROLOGY
- Identifying Non–Duchenne Muscular Dystrophy–Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs
- (2016) Michele A. Gatheridge et al. JAMA Neurology
- A Phase 1/2a Follistatin Gene Therapy Trial for Becker Muscular Dystrophy
- (2015) Jerry R Mendell et al. MOLECULAR THERAPY
- Progression and variation of fatty infiltration of the thigh muscles in Duchenne muscular dystrophy, a muscle magnetic resonance imaging study
- (2015) Wenzhu Li et al. NEUROMUSCULAR DISORDERS
- Cystic fibrosis newborn screening: A model for neuromuscular disease screening?
- (2014) Michele A. Scully et al. ANNALS OF NEUROLOGY
- A 19-year-old ambulant Duchenne patient with stunted growth on long-term corticosteroids
- (2014) Luciano Merlini NEUROMUSCULAR DISORDERS
- A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy
- (2014) Jean K. Mah et al. NEUROMUSCULAR DISORDERS
- Eteplirsen for the treatment of Duchenne muscular dystrophy
- (2013) Jerry R. Mendell et al. ANNALS OF NEUROLOGY
- Update on the Treatment of Duchenne Muscular Dystrophy
- (2013) Louise R. Rodino-Klapac et al. Current Neurology and Neuroscience Reports
- Decision-making process for conditions nominated to the Recommended Uniform Screening Panel: statement of the US Department of Health and Human Services Secretary’s Advisory Committee on Heritable Disorders in Newborns and Children
- (2013) Alex R. Kemper et al. GENETICS IN MEDICINE
- All-Cause Mortality and Cardiovascular Outcomes With Prophylactic Steroid Therapy in Duchenne Muscular Dystrophy
- (2013) Gernot Schram et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy
- (2013) Jerry R. Mendell et al. MUSCLE & NERVE
- Quality improvement in neurology: Amyotrophic lateral sclerosis quality measures: Report of the Quality Measurement and Reporting Subcommittee of the American Academy of Neurology
- (2013) R. G. Miller et al. NEUROLOGY
- Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?
- (2013) M. A. Scully et al. NEUROLOGY
- Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
- (2013) Anne M. Connolly et al. NEUROMUSCULAR DISORDERS
- Evidence-based path to newborn screening for duchenne muscular dystrophy
- (2012) Jerry R. Mendell et al. ANNALS OF NEUROLOGY
- Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14-year follow-up
- (2012) Luciano Merlini et al. MUSCLE & NERVE
- What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Servicesʼ Advisory Committee on Heritable Disorders in Newborns and Children
- (2011) Cynthia F. Hinton et al. GENETICS IN MEDICINE
- Disparities in the diagnostic process of Duchenne and Becker muscular dystrophy
- (2011) Caleb Holtzer et al. GENETICS IN MEDICINE
- The context and approach for the California newborn screening short- and long-term follow-up data system: Preliminary findings
- (2010) Lisa Feuchtbaum et al. GENETICS IN MEDICINE
- Delayed Diagnosis in Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)
- (2009) Emma Ciafaloni et al. JOURNAL OF PEDIATRICS
- Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis
- (2009) Drucy Borowitz et al. JOURNAL OF PEDIATRICS
- Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care
- (2009) Katharine Bushby et al. LANCET NEUROLOGY
- Long-term follow-up after diagnosis resulting from newborn screening: Statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children
- (2008) Alex R Kemper et al. GENETICS IN MEDICINE
- Ethical, Legal, and Social Concerns About Expanded Newborn Screening: Fragile X Syndrome as a Prototype for Emerging Issues
- (2008) D. B. Bailey et al. PEDIATRICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started