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JAMA|October 29, 1997
Diagnosis and treatment of Alzheimer disease and related disorders. Consensus statement of the American Association for Geriatric Psychiatry, the Alzheimer's Association, and the American Geriatrics SocietyG W Small, P V Rabins, P P Barry, et al.
Analytical and Bioanalytical Chemistry|May 3, 2011
Ultra-trace analysis of 36Cl by accelerator mass spectrometry: an interlaboratory studyS Merchel, W Bremser, V Alfimov, et al.
Muscle & Nerve|February 2, 2019
Twice-weekly glucocorticosteroids in infants and young boys with Duchenne muscular dystrophyAnne M Connolly, Craig M Zaidman, Paul T Golumbek, et al.
Annals of Neurology|January 23, 2015
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45Andrew R Findlay, Nicolas Wein, Yuuki Kaminoh, et al.
Brain : a Journal of Neurology|June 25, 2024
TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestationsGage P Kosmanopoulos, Jack K Donohue, Maya Hoke, et al.
JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Mechanistic Insights into Tumorigenesis from Serum ProteinsValur Emilsson, Valborg Gudmundsdottir, Sean Bankier, et al.
Annals of Clinical and Translational Neurology|September 12, 2019
Dominant collagen XII mutations cause a distal myopathyPayam Mohassel, Teerin Liewluck, Ying Hu, et al.
Nature Medicine|December 8, 2025
Intrathecal onasemnogene abeparvovec in treatment-naive patients with spinal muscular atrophy: a phase 3, randomized controlled trialCrystal M Proud, Dũng Chí Vũ, Jo M Wilmshurst, et al.
American Journal of Physical Medicine & Rehabilitation|May 8, 2018
Two-Year Longitudinal Changes in Lower Limb Strength and Its Relation to Loss in Function in a Large Cohort of Patients With Duchenne Muscular DystrophyAbhinandan Batra, Ann Harrington, Donovan J Lott, et al.
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