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Clinical Pharmacology and Therapeutics|December 4, 2018
Oral Chaperone Therapy Migalastat for Treating Fabry Disease: Enzymatic Response and Serum Biomarker Changes After 1 YearJonas Müntze, Daniel Gensler, Octavian Maniuc, et al.
Orphanet Journal of Rare Diseases|August 17, 2018
Characterization of vertigo and hearing loss in patients with Fabry diseaseMaria Köping, Wafaa Shehata-Dieler, Dieter Schneider, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|May 26, 2018
Value of the CHA2DS2-VASc score and Fabry-specific score for predicting new-onset or recurrent stroke/TIA in Fabry disease patients without atrial fibrillationDan Liu, Kai Hu, Marie Schmidt, et al.
Circulation. Cardiovascular Genetics|October 12, 2017
α-Galactosidase A Genotype N215S Induces a Specific Cardiac Variant of Fabry DiseaseDaniel Oder, Dan Liu, Kai Hu, 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.
Plos One|August 2, 2017
Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factorsMaarten Arends, Marieke Biegstraaten, Derralynn A Hughes, et al.
Journal of Medical Genetics|February 14, 2018
Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort studyMaarten Arends, Marieke Biegstraaten, Christoph Wanner, et al.
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