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American Journal of Medical Genetics. Part A|March 8, 2022
Neurological features of Noonan syndrome and related RASopathies: Pain and nerve enlargement characterized by nerve ultrasoundWillem De Ridder, Baziel van Engelen, Nens van AlfenClinical Science (London, England : 1979)|July 10, 2003
Quadriceps weakness in a family with nemaline myopathy: influence of knee angleKarin Gerrits, Inge Gommans, Baziel van Engelen, et al.Clinical Physiology and Functional Imaging|June 15, 2007
Contractile properties of knee-extensors in one single family with nemaline myopathy: central and peripheral aspects of muscle activationKarin Gerrits, Inge Pauw-Gommans, Baziel van Engelen, et al.Neurology|April 3, 2016
Quantitative MRI reveals decelerated fatty infiltration in muscles of active FSHD patientsBarbara Janssen, Nicoline Voet, Alexander Geurts, et al.Disability and Rehabilitation|November 12, 2009
Classification of employment factors according to the International Classification of Functioning, Disability and Health in patients with neuromuscular diseases: a systematic reviewMarie-Antoinette Minis, Yvonne Heerkens, Josephine Engels, et al.Clinical Genetics|February 23, 2020
Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophyAnna Greco, Remko Goossens, Baziel van Engelen, et al.International Journal of Speech-Language Pathology|September 27, 2017
Reference values of maximum performance tests of speech productionSimone Knuijt, Johanna Kalf, Baziel Van Engelen, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 6, 2003
Auditory processing in patients with Charcot-Marie-Tooth disease type 1AKarin Neijenhuis, Andy Beynon, Ad Snik, et al.HGG Advances|January 12, 2024
PABPN1 loss-of-function causes APA-shift in oculopharyngeal muscular dystrophyMilad Shademan, Hailiang Mei, Baziel van Engelen, et al.Pageof 6