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International Journal of Molecular Sciences|July 9, 2022
Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic NeuropathyMilena Ślęczkowska, Rowida Almomani, Margherita Marchi, et al.Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.Neuromuscular Disorders : NMD|May 24, 2016
The epidemiology of neuromuscular disorders: Age at onset and gender in the NetherlandsJohanna C W Deenen, Pieter A van Doorn, Catharina G Faber, et al.The Journal of Clinical Investigation|July 26, 2008
Noninvasive diagnosis of ruptured peripheral atherosclerotic lesions and myocardial infarction by antibody profilingKitty B J M Cleutjens, Birgit C G Faber, Mat Rousch, et al.Tijdschrift Voor Psychiatrie|March 6, 2010
[Routine Outcome Monitoring for patients with severe mental illness: a consensus document]C L Mulder, M van der Gaag, R Bruggeman, et al.Human Molecular Genetics|November 22, 2024
The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fractureBenjamin G Faber, Monika Frysz, Jaiyi Zheng, et al.Neurology|June 3, 2021
Prospective Evaluation of Health Care Provider and Patient Assessments in Chemotherapy-Induced Peripheral NeurotoxicityPaola Alberti, Davide P Bernasconi, David R Cornblath, et al.Journal of Neurology|June 9, 2005
Inclusion body myositis. Clinical features and clinical course of the disease in 64 patientsUmesh A Badrising, Marion L C Maat-Schieman, Johannes C van Houwelingen, et al.Circulation|December 21, 2005
Disruption of the cathepsin K gene reduces atherosclerosis progression and induces plaque fibrosis but accelerates macrophage foam cell formationE Lutgens, S P M Lutgens, B C G Faber, et al.Neurology|December 30, 2004
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositisU A Badrising, G M Th Schreuder, M J Giphart, et al.Pageof 32