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Osteoarthritis and Cartilage|November 7, 2023
Comparison between UK Biobank and Shanghai Changfeng suggests distinct hip morphology may contribute to ethnic differences in the prevalence of hip osteoarthritisJiayi Zheng, Monika Frysz, Benjamin G Faber, et al.
Muscle & Nerve|September 27, 2014
Contact heat evoked potentials: normal values and use in small-fiber neuropathyVera Lagerburg, Mayienne Bakkers, Anne Bouwhuis, et al.
Brain : a Journal of Neurology|February 4, 2020
Differential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathyJulie I R Labau, Mark Estacion, Brian S Tanaka, et al.
Blood|July 5, 2003
Vasculin, a novel vascular protein differentially expressed in human atherogenesisAnn P J J Bijnens, Ann Gils, Barry Jutten, et al.
Frontiers in Cardiovascular Medicine|July 16, 2025
Evaluation of echocardiography monitoring in myotonic dystrophy type 1 patientsD S H Bovenkerk, C E W Janssen, F M A Van den Heuvel, et al.
Plos One|October 7, 2020
Vibration threshold in non-diabetic subjectsSvea Nolte, Marco van Londen, Jan Willem J Elting, et al.
Neuromuscular Disorders : NMD|April 3, 2018
Prevalence and mutation spectrum of skeletal muscle channelopathies in the NetherlandsB C Stunnenberg, J Raaphorst, J C W Deenen, et al.
Neuromuscular Disorders : NMD|August 31, 2024
Comprehensive four-year disease progression assessment of myotonic dystrophy type 1Leandre A la Fontaine, Johanna E Bruijnes, Fran Hp Smulders, et al.
Human Molecular Genetics|January 19, 2010
Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patientsClaudia Braida, Rhoda K A Stefanatos, Berit Adam, et al.
The Lancet. Neurology|June 24, 2018
Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trialKees Okkersen, Cecilia Jimenez-Moreno, Stephan Wenninger, et al.
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