Fabry disease: overall effects of agalsidase alfa treatment-Reference-Cited by-同舟云学术

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Fabry disease: overall effects of agalsidase alfa treatment

Published:2004-12 Issue:12 Volume:34 Page:838-844
ISSN:0014-2972
Container-title:European Journal of Clinical Investigation
language:en
Short-container-title:Eur J Clin Invest

Author:

Beck M.,Ricci R.,Widmer U.,Dehout F.,de Lorenzo A. Garcia,Kampmann C.,Linhart A.,Sunder-Plassmann G.,Houge G.,Ramaswami U.,Gal A.,Mehta A.

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.2004.01424.x/fullpdf

Reference22 articles.

1. Prevalence of Lysosomal Storage Disorders

2. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males

3. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females

4. Natural History of Fabry Renal Disease

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2. Effects of Enzyme Replacement Therapy on Cardiac MRI Findings in Fabry Disease: A Systematic Review and Meta-Analysis;Radiology: Cardiothoracic Imaging;2024-06-01

3. Fabry disease: development and progression of left ventricular hypertrophy despite long-term enzyme replacement therapy;Heart;2024-05-15

4. Updated Evaluation of Agalsidase Alfa Enzyme Replacement Therapy for Patients with Fabry Disease: Insights from Real-World Data;Drug Design, Development and Therapy;2024-04

5. Polymer-based drug delivery systems under investigation for enzyme replacement and other therapies of lysosomal storage disorders;Advanced Drug Delivery Reviews;2023-06

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