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Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
Breast (Edinburgh, Scotland)|May 2, 2021
Effect of a health literacy training program for surgical oncologists and specialized nurses on disparities in referral to breast cancer genetic testingJeanine A M van der Giessen, Sandra van Dulmen, Mary E Velthuizen, et al.
BMC Neurology|August 18, 2016
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)Rianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.
American Journal of Medical Genetics. Part A|July 3, 2024
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort studyFieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|May 17, 2011
Respiratory sensitization: advances in assessing the risk of respiratory inflammation and irritationRob Vandebriel, Conchita Callant Cransveld, Daan Crommelin, 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.
Brain Communications|February 8, 2023
Neuromuscular symptoms in patients with RYR1-related malignant hyperthermia and rhabdomyolysisLuuk R van den Bersselaar, Heinz Jungbluth, Nick Kruijt, et al.
International Journal of Cancer|January 4, 2024
Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associationsDilys D Weijers, Steffen Hirsch, Jette J Bakhuizen, et al.
European Journal of Human Genetics : EJHG|November 23, 2017
Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2Richard Jlf Lemmers, Patrick J van der Vliet, Judit Balog, et al.
Molecular Genetics and Metabolism|August 6, 2013
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibersValeria Guglielmi, Gaetano Vattemi, Francesca Gualandi, et al.
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