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Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome SurveyUma Ramaswami, Catharina Whybra, Rosella Parini, et al.Revue Medicale De La Suisse Romande|November 9, 2002
[Fabry disease: diagnostic due of substitutive enzyme-therapy]Frédéric Barbey, Urs Widmer, Michel Burnier, et al.AJR. American Journal of Roentgenology|November 23, 2006
Segmental arterial mediolysis: CTA findings at presentation and follow-upMaren Michael, Urs Widmer, Simon Wildermuth, et al.Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.Kidney International|April 21, 2005
Anemia is a new complication in Fabry disease: data from the Fabry Outcome SurveyJulia Kleinert, François Dehout, Andreas Schwarting, et al.American Journal of Hypertension|August 1, 2006
Prevalence of uncontrolled hypertension in patients with Fabry diseaseJulia Kleinert, François Dehout, Andreas Schwarting, et al.Current Pharmaceutical Biotechnology|January 18, 2011
Mucopolysaccharidosis Type II (Hunter Syndrome): clinical picture and treatmentMichael BeckActa Paediatrica (Oslo, Norway : 1992). Supplement|May 25, 2006
The Mainz Severity Score Index (MSSI): development and validation of a system for scoring the signs and symptoms of Fabry diseaseMichael BeckHuman Genetics|November 8, 2006
New therapeutic options for lysosomal storage disorders: enzyme replacement, small molecules and gene therapyMichael BeckPageof 23