Agalsidase alfa – a preparation for enzyme replacement therapy in Anderson–Fabry disease
Author:
Publisher
Informa Healthcare
Subject
Pharmacology (medical),Pharmacology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1517/13543784.11.6.851
Reference29 articles.
1. Enzymatic Defect in Fabry's Disease
2. Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease
3. Anderson-Fabry disease: Clinical manifestations of disease in female heterozygotes
4. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males
5. Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene.
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4. Fabry disease, enzyme replacement therapy and the significance of antibody responses;Journal of Inherited Metabolic Disease;2011-10-25
5. Effect of Reduced Agalsidase Beta Dosage in Fabry Patients: The Australian Experience;JIMD Reports;2011
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