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Muscle & Nerve|January 24, 2025
Prophylactic Use of Cardiac Medications and Survival in Duchenne Muscular DystrophyKristin M Conway, Shiny Thomas, Tahereh Neyaz, et al.
Neurology|January 16, 2008
The hypocretin neurotransmission system in myotonic dystrophy type 1E Ciafaloni, E Mignot, V Sansone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2011
Disparities in the diagnostic process of Duchenne and Becker muscular dystrophyCaleb Holtzer, F John Meaney, Jennifer Andrews, et al.
Respiratory Care|August 11, 2016
Respiratory Care Received by Individuals With Duchenne Muscular Dystrophy From 2000 to 2011Jennifer G Andrews, Aida Soim, Shree Pandya, et al.
Neuroepidemiology|January 9, 2023
Racial and Ethnic Differences in Timing of Diagnosis and Clinical Services Received in Duchenne Muscular DystrophyJoshua R Mann, Yanan Zhang, Suzanne McDermott, et al.
Pediatrics|June 22, 2018
Implementation of Duchenne Muscular Dystrophy Care ConsiderationsJennifer G Andrews, Kristin Conway, Christina Westfield, et al.
Neuromuscular Disorders : NMD|July 26, 2017
Delayed onset of ambulation in boys with Duchenne muscular dystrophy: Potential use as an endpoint in clinical trialsJacob J Gissy, Teresa Johnson, Deborah J Fox, et al.
Muscle & Nerve|May 9, 2024
Patient- and caregiver-reported impact of symptoms in Duchenne muscular dystrophySpencer Rosero, Jennifer Weinstein, Jamison Seabury, et al.
Health and Quality of Life Outcomes|February 12, 2017
Perceived quality of life among caregivers of children with a childhood-onset dystrophinopathy: a double ABCX model of caregiver stressors and perceived resourcesNatalia Frishman, Kristin Caspers Conway, Jennifer Andrews, et al.
Neuromuscular Disorders : NMD|May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research NetworkPangaja Paramsothy, Yinding Wang, Bo Cai, et al.
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