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Nederlands Tijdschrift Voor Geneeskunde|October 6, 2005
[The spectrum of hereditary skeletal-muscle channelopathies]J Trip, G Drost, H B Ginjaar, et al.Molecular Therapy. Methods & Clinical Development|October 9, 2023
Archival skin biopsy specimens as a tool for miRNA-based diagnosis: Technical and post-analytical considerationsMirna Andelic, Margherita Marchi, Stefania Marcuzzo, et al.Muscle & Nerve|May 30, 2013
Small fibers, large impact: quality of life in small-fiber neuropathyMayienne Bakkers, Catharina G Faber, Janneke G J Hoeijmakers, et al.Plos One|October 21, 2015
Reconstructing the Rasch-Built Myotonic Dystrophy Type 1 Activity and Participation ScaleMieke C E Hermans, Janneke G J Hoeijmakers, Catharina G Faber, et al.Current Opinion in Lipidology|September 28, 2002
Genes potentially involved in plaque ruptureBirgit C G Faber, Sylvia Heeneman, Mat J A P Daemen, et al.European Journal of Neurology|February 23, 2019
The minimum clinically important difference: which direction to takeT H P Draak, B T A de Greef, C G Faber, et al.Toxicology|August 25, 2025
FOXO3 mediated gene expression modulates doxorubicin sensitivity in human cardiomyocytesJ G Faber, M van Herwijnen, D Hauser, et al.Frontiers in Endocrinology|October 21, 2024
Sex differences in the radiographic and symptomatic prevalence of knee and hip osteoarthritisBenjamin G Faber, Fiona Macrae, Mijin Jung, et al.The British Journal of Surgery|February 1, 1978
Gallstone disease presenting as septicaemic shockR G Faber, S Z Ibrahim, D M Thomas, et al.Current Diabetes Reports|August 22, 2014
The role of sodium channels in painful diabetic and idiopathic neuropathyGiuseppe Lauria, Dan Ziegler, Rayaz Malik, et al.Pageof 32