Author:
Christensen Erik I.,Zhou Qun,Sørensen Søren S.,Rasmussen Åse K.,Jacobsen Christian,Feldt-Rasmussen Ulla,Nielsen Rikke
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
Reference30 articles.
1. Desnick RJ, Ioannou YA, Eng CM: Alpha-galactosidase A deficiency: Fabry disease. In: The Metabolic and Molecular Bases of Inherited Disease, 8th Ed., edited by Scriver CR, Beaudet AL, Sly WS, Valle D, New York, McGraw-Hill, 2006 , pp 3733 –3774
2. Anderson-Fabry disease: Clinical manifestations of disease in female heterozygotes
3. Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey
4. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy
5. Fabry Disease: Preclinical Studies Demonstrate the Effectiveness of α-Galactosidase A Replacement in Enzyme-Deficient Mice
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