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Rare diseases / Medicine / Fabry disease / Genetics / Enzymes / Galactosides / Lysosomal storage disease / Alpha-galactosidase / Mutation / Biology / Health / Lipid storage disorders


Andreotti et al. Orphanet Journal of Rare Diseases 2011, 6:66 http://www.ojrd.com/content[removed]RESEARCH Open Access
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City

Garman / Pozzuoli / Petsko / Rockville / Chiang / Ashley / Caserta / Winchester / Oxford / Benson / Topaloglu / Napoli / Berlin / Cambridge / Johnson / Milan / Naples / /

Company

Clague AE / IgG / Pearson / BioMed Central Ltd. / Genzyme Europe B. V. NL / Bio-Rad / Suzuki / Microsoft / Creative Commons / /

Country

Germany / Netherlands / Italia / Italy / United States / United Kingdom / /

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IndustryTerm

active site / Therapy of Fabry disease / therapy for Fabry disease / chemical / chemicals / /

MedicalCondition

DF / Rare Diseases / angiokeratomas / JE / progressive vascular disease / Background Fabry Disease / ORF / rare disorder / phenylketonuria / MS / common diseases / Anderson-Fabry disease / disease / amyloidosis / Fabry disease / diseases / hypohidrosis / lysosomal storage diseases / corneal opacity / pan-ethnic disorder / disorders / /

MedicalTreatment

intravenous infusions / enzyme replacement therapy / /

Person

J. Cheng / Maria Malanga / Federico II / J. Jenkins / Maria Vittoria / Arch Biochem Biophys / Cary Eclypse-Varian / S. Lovell / /

Position

counsel / author / Fisher / representative / forward / reporter / /

Product

Sanyo R227 Portable Audio Device / Fabrazyme / /

ProgrammingLanguage

J / /

ProvinceOrState

Alaska / South Dakota / South Carolina / Mississippi / Georgia / /

PublishedMedium

The Biochemical journal / /

RadioStation

Katz / /

Technology

alpha / Genomics / ADC / bioinformatics / X-ray / directed mutagenesis / genotyping / Genotype / /

URL

http /

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