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Glycoproteinosis / Lysosomal storage disease / Alpha-mannosidosis / Sialidosis / Fucosidosis / Pseudo-Hurler polydystrophy / I-cell disease / Mucolipidosis / Aspartylglucosaminuria / Health / Rare diseases / Biology


What are Glycoprotein Storage Diseases? ? They are very rare, progressive and largely untreatable inherited genetic defects.
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Document Date: 2014-09-02 17:45:22


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City

Baltimore / /

Company

Greenwood Genetic Centre / AMP / ISMRD / /

Country

United States / New Zealand / /

Currency

USD / /

Event

Business Partnership / Product Issues / /

Facility

Penguin Cafe / /

MedicalCondition

Glycoprotein diseases / bone disease / •Beta Mannosidosis •Galactosialidosis •Schindler Disease •Aspartylglucosaminuria •Mucolipidosis II / diseases / •Alpha Mannosidosis •Fucosidosis •Mucolipidosis III / Matthew Fucosidosis ISMRD Supports The Following Diseases / Glycoprotein Storage Diseases / Lysosomal diseases / deficiency / Mucolipidosis / /

Organization

National Institute of Health / International Society for Mannosidosis & Related Diseases / /

Person

Matthew Fucosidosis / Paul Murphy / Alex Sialidosis Brooke / Debora Murphy / Taryn Alpha / /

Position

leading advocate / •Sialidosis The International Advocate / fundraiser / /

Product

trafficking / /

ProgrammingLanguage

ML / /

ProvinceOrState

Maryland / Michigan / /

PublishedMedium

the Natural History / Natural History / /

Technology

Alpha / /

URL

www.ismrd.org / /

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