Showing results (741-750 of 831) with videos related to

Sort By:
Pageof 84
Neuromuscular Disorders : NMD|August 8, 2024
Population-based incidence rates of 15 neuromuscular disorders: a nationwide capture-recapture study in the NetherlandsJohanna C W Deenen, Corinne G C Horlings, Nicol C Voermans, et al.
American Journal of Human Genetics|November 27, 2010
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
Human Molecular Genetics|September 24, 2021
High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effectRichard J L F Lemmers, Patrick J van der Vliet, David San Leon Granado, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|May 24, 2011
Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7K van Engelen, A V Postma, J B A van de Meerakker, et al.
Breast Cancer Research and Treatment|July 15, 2019
Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriersBernadette A M Heemskerk-Gerritsen, Agnes Jager, Linetta B Koppert, et al.
Brain Communications|December 16, 2024
Musicality and social cognition in dementia: clinical and anatomical associationsJochum J van 't Hooft, Willem L Hartog, Michelle Braun, et al.
Journal of Medical Genetics|September 22, 2022
Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial casesInge M M Lakeman, Mar D M Rodríguez-Girondo, Andrew Lee, et al.
Neuromuscular Disorders : NMD|August 24, 2024
A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the NetherlandsEsmee S B van Kleef, Sanne A J H van de Camp, Jan T Groothuis, et al.
Journal of Cachexia, Sarcopenia and Muscle|March 13, 2026
Evaluation of Dysphagia in Myositis and Muscular Dystrophy Using Real-Time MRI and Quantitative Muscle UltrasoundRachel Zeng, Anke Rietveld, Omar Al-Bourini, et al.
Pageof 84