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European Journal of Pain (London, England)|February 22, 2011
The relation between small nerve fibre function, age, disease severity and pain in Fabry diseaseMarieke Biegstraaten, Andreas Binder, Rainer Maag, et al.Journal of Inherited Metabolic Disease|November 15, 2014
Hearing loss in adult patients with Fabry disease treated with enzyme replacement therapyEefje B Suntjens, Bouwien E Smid, Marieke Biegstraaten, et al.Orphanet Journal of Rare Diseases|November 30, 2018
Oncologic orphan drugs approved in the EU - do clinical trial data correspond with real-world effectiveness?Yvonne Schuller, Marieke Biegstraaten, Carla E M Hollak, et al.Molecular Genetics and Metabolism|April 14, 2012
Small fiber neuropathy in Fabry diseaseMarieke Biegstraaten, Carla E M Hollak, Mayienne Bakkers, et al.JIMD Reports|November 14, 2015
In Patients with an α-Galactosidase A Variant, Small Nerve Fibre Assessment Cannot Confirm a Diagnosis of Fabry DiseaseLinda van der Tol, Camiel Verhamme, Ivo N van Schaik, et al.Journal of Medical Genetics|January 18, 2015
Plasma globotriaosylsphingosine in relation to phenotypes of Fabry diseaseBouwien E Smid, Linda van der Tol, Marieke Biegstraaten, et al.Brain : a Journal of Neurology|August 10, 2010
Peripheral neuropathy in adult type 1 Gaucher disease: a 2-year prospective observational studyMarieke Biegstraaten, Eugen Mengel, Laszlo Maródi, et al.Journal of the American Society of Nephrology : JASN|December 17, 2016
Characterization of Classical and Nonclassical Fabry Disease: A Multicenter StudyMaarten Arends, Christoph Wanner, Derralynn Hughes, et al.Molecular Genetics and Metabolism|May 13, 2017
Favourable effect of early versus late start of enzyme replacement therapy on plasma globotriaosylsphingosine levels in men with classical Fabry diseaseMaarten Arends, Frits A Wijburg, Christoph Wanner, et al.Journal of Neurology|August 11, 2012
FabryScan: a screening tool for early detection of Fabry diseaseKathrin Arning, Dennis Naleschinski, Rainer Maag, et al.Pageof 3