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Journal of Child Neurology|March 9, 2010
Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophyDennis J Matthews, Katherine A James, Lisa A Miller, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 13, 2002
Omeprozole therapy in pediatric patients after liver and intestinal transplantationStuart S Kaufman, Elizabeth Ruby Lyden, Cindy R Brown, et al.
International Journal of Pharmaceutics|November 20, 2021
A mucoadhesive biodissolvable thin film for localized and rapid delivery of lidocaine for the treatment of vestibulodyniaDenali K Dahl, Ashlyn N Whitesell, Preetika Sharma-Huynh, et al.
HIV Medicine|February 27, 2016
Incorporating HIV/hepatitis B virus/hepatitis C virus combined testing into routine blood tests in nine UK Emergency Departments: the "Going Viral" campaignC Orkin, S Flanagan, E Wallis, et al.
JAMA Neurology|August 28, 2020
Efficacy and Safety of 2 Fingolimod Doses vs Glatiramer Acetate for the Treatment of Patients With Relapsing-Remitting Multiple Sclerosis: A Randomized Clinical TrialBruce A C Cree, Myla D Goldman, John R Corboy, et al.
Hepatology Communications|May 16, 2018
Liver-enriched transcription factor expression relates to chronic hepatic failure in humansJorge Guzman-Lepe, Eduardo Cervantes-Alvarez, Alexandra Collin de l'Hortet, et al.
Mindfulness|April 20, 2026
"Noticing the Way that I'm Noticing Pain": A Qualitative Analysis of Therapeutic Progression in Mindfulness-Oriented Recovery Enhancement for Patients with Lumbosacral Radicular PainRyan S Wexler, Wade Balsamo, Devon J Fox, et al.
Best Practice & Research. Clinical Anaesthesiology|September 13, 2021
Framework for creating an incident command center during crisesAlan D Kaye, Elyse M Cornett, Anusha Kallurkar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 25, 2012
Setting a research agenda for progressive multiple sclerosis: the International Collaborative on Progressive MSRobert J Fox, Alan Thompson, David Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 21, 2013
Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndromeZhong Deng, Galina Glousker, Aliah Molczan, et al.
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