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Muscle & Nerve|June 23, 2025
Pain Experiences and Prescription Pain Medications Among People With Selected Muscular Dystrophies in the Muscular Dystrophy Surveillance, Tracking, and Research NetworkJonathan Suhl, Kristin M Conway, Shiny Thomas, et al.
Journal of Rehabilitation Research and Development|January 1, 1997
Design and pilot testing of the DVA/Seattle Footwear System for diabetic patients with foot insensitivityG E Reiber, D G Smith, D A Boone, et al.
Neurology|February 4, 2012
β-Amyloid burden in healthy aging: regional distribution and cognitive consequencesK M Rodrigue, K M Kennedy, M D Devous, et al.
Children (Basel, Switzerland)|October 23, 2021
Characteristics of Clinical Trial Participants with Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)Katherine D Mathews, Kristin M Conway, Amber M Gedlinske, et al.
Neurology|January 9, 2015
Urologic and gastrointestinal symptoms in the dystroglycanopathiesCameron D Crockett, Laura A Bertrand, Christopher S Cooper, et al.
Frontiers in Public Health|August 1, 2025
Factors influencing implementation of a self-measured blood pressure program in community health centers: an implementation mapping approachSerena A Rodriguez, Fernanda Velasco-Huerta, Mahalia Sampson-Ansah, et al.
Annals of Clinical and Translational Neurology|September 29, 2024
Onasemnogene-abeparvovec administration to premature infants with spinal muscular atrophyStephen M Brown, Aparna S Ajjarapu, Divya Ramachandra, et al.
Journal of Inflammation|January 1, 1995
NF-kappa B is activated during acute inflammation in vivo in association with elevated endothelial cell adhesion molecule gene expression and leukocyte recruitmentA M Manning, F P Bell, C L Rosenbloom, et al.
British Medical Journal|March 13, 1976
Hormonal assessment before and after vasectomyD C Skegg, J D Mathews, J Guillebaud, et al.
American Journal of Human Genetics|August 1, 1992
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)K A Mills, K H Buetow, Y Xu, et al.
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