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Lipid storage disorders / Fabry disease / Alpha-galactosidase / Enzyme replacement therapy / Globotriaosylceramide / Placebo / Health / Medicine / Rare diseases


  The Journal of Rare Disorders CochraneCorner 
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Document Date: 2015-01-07 11:10:15

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File Size: 217,69 KB

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City

New York / Botucatu / Cambridge / /

Company

Clague AE / GE / Genzyme / /

Country

Brazil / /

Facility

University School / /

IndustryTerm

Therapy for Anderson‐Fabry Disease / /

MedicalCondition

Fabry’s disease / pain / Fabry disease / Rare Disorders / ssue injury / lysosomal storage disorders / Anderson‐Fabry Disease / deficiency / later‐onset Fabry disease / X‐linked recessive mul systemic disorder / Renal and cardiac failure / /

MedicalTreatment

Enzyme replacement therapy / intravenous infusion / /

Organization

Universidade Estadual Paulista / 2Anesthesiology Department / New York University School of Medicine / Botucatu Medical School / /

Person

Gregory M. Pastores / Paulo Nascimento / Regina P. El Dib / /

Position

Major / /

Product

rela / Fabrazyme / /

ProvinceOrState

New York / /

Technology

alpha / /

SocialTag