search:fabry disease therapy相關網頁資料

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日期:2024-08-04
1. Drugs. 2009 Nov 12;69(16):2179-205. doi: 10.2165/11318300-000000000-00000. Enzyme replacement therapy for Fabry disease: a systematic review of available evidence. Schaefer RM, Tylki-Szymańska A, Hilz MJ. Fabry disease is a progressive and life ......
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日期:2024-08-10
Fabry disease, also called Anderson-Fabry disease, is the second most prevalent lysosomal storage disorder after Gaucher's disease. It is an X-linked inborn error of the glycosphingolipid metabolic pathway. This results in accumulation of globotriaos...
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日期:2024-08-07
Who discovered Fabry Disease? Fabry disease or otherwise known as (less commonly): anderson-fabry disease, angiokeratoma corporis diffusum hereditary dystopic lipidosis alpha-galactosidase A deficiency gla deficiency ceramide trihexosidase deficiency Fabr...
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Learn about Fabry disease, an inherited disorder caused by deficiency of the alpha-galactosidase A enzyme, and Fabrazyme enzyme replacement therapy....
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Treatment. Both symptom management and enzyme replacement therapy can play a role in the medical management of patients with Fabry disease....
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日期:2024-08-09
2010年7月23日 - Enzyme replacement therapy is available for the treatment of Fabry disease, but it is a costly, intravenous treatment. Alternative therapeutic ......
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2014年11月24日 - Fabry disease, also called Anderson-Fabry disease, is the second most prevalent lysosomal storage disorder after Gaucher's disease. It is an ......
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日期:2024-08-08
WebMD looks at the causes, symptoms, and treatment of Fabry disease, an inherited condition that brings on a variety of symptoms, including pain in the hands ......