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National MPS Society - We Help Cure, Support, & Advocate for MPS & ML

We support life-saving research for mucopolysaccharidosis (MPS) & mucolipidosis (ML), and we provide community resources, support, & more.
Categories: Non-Profit/Advocacy/NGO, Health and Wellness
Topics: advocate for mps, cpap vs bipap, mps, mps disease, mps society, national mps society, sanfilippo syndrome, support for families. research for a cure, we help cure, what is mps

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Sites similar to mpssociety.org - Top 33 mpssociety.org alternatives

mps1disease.com

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Gateway Page
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mpssociety.org.uk

mpssociety.org.uk mpssociety.org.uk           
MPS Society | Support for MPS, Fabry and related diseases in the United Kingdom
The Society for Mucopolysaccharide Diseases (MPS Society) provides professional support to individuals and families affected by MPS, Fabry and related lysosomal storage diseases. Contact our helpline Monday-Friday 9-5pm on 0345 389 9901 or email us at [email protected]


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jonahsjustbegun.org

jonahsjustbegun.org jonahsjustbegun.org           
Jonah's Just Begun - Curing SanFilippo Disease One Day at a Time
Jonah's Just Begun - Curing SanFilippo Disease One Day at a Time


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mpssociety.in

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MPS Society – Best CBSE Affiliated School In Bhiwadi
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sanfilippo.org.au

sanfilippo.org.au sanfilippo.org.au           
Sanfilippo Children's Foundation
Sanfilippo is a rare genetic condition that causes fatal brain damage. It is a type of childhood dementia and most patients never reach adulthood. But there is hope. Researchers around the world are working hard to find effective treatments.

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teamsanfilippo.org

teamsanfilippo.org teamsanfilippo.org           
Team Sanfillipo — Parents united to find a cure or treatments
Cure Sanfilippo, Gene therapy, Get help for Sanfilippo, MPS, MPS III, Rare diseases, lysosomal disease, and Fundraising


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Phoenix Nest Inc.
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raremark.com

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Rare Disease Health Info & Community
Learn about numerous rare diseases including symptoms, diagnosis, treatment, patient stories & more from a rare disease community perspective.

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curesff.org

curesff.org curesff.org           
Cure Sanfilippo Foundation | Accelerating a cure for Sanfilippo Syndrome
Every parents dreams of their child's future. Sanfilippo Syndrome takes that away and replaces it with pain and suffering before death. Cure Sanfilippo Foundation advocates for and funds research to accelerate discovery of a cure or treatment options for children with Sanfilippo Syndrome (MPS III).

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hunterpatients.com

hunterpatients.com hunterpatients.com           
Learn About Hunter Syndrome
This website is a resource for people with Hunter syndrome (MPS II), their family and friends, and healthcare providers. Learn more.

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lysosomaldiseasenetwork.org

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Home - Lysosomal Disease Network
Home - Lysosomal Disease Network

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biomarin.com

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BioMarin Pharmaceutical Inc.
BioMarin is a world leader in developing and commercializing innovative biopharmaceuticals for rare diseases driven by genetic causes.

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Patient | Naglazyme
Welcome to WordPress. This is your first post. Edit or delete it, then start blogging!


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Svenska MPS-f�reningen
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sanfilipponews.com

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The Web's Daily Resource for Sanfilippo Syndrome News

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Ultragenyx—Treatment of Rare and Ultrarare Genetic Diseases
Ultragenyx is focused on developing first-ever approved treatments for rare and ultrarare diseases and moving the rare disease community forward.

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mpssociety.ca

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Home - mpssociety
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vimizim.com

vimizim.com vimizim.com           
Treatment for Morquio A (MPS IVA) |VIMIZIM® (elosulfase alfa)
VIMIZIM® (elosulfase alfa) is the first and only enzyme replacement therapy approved for people with Morquio A. View important safety information, including risk of anaphylaxis.

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mpslimited.com

mpslimited.com mpslimited.com           
MPS Limited: Make Learning Smarter
MPS is a leading global provider of platforms and content solutions for the digital world. MPS also partners with companies to deliver exceptional content on time and under budget. We offer a full scope of Content Solutions including Content Authoring and Development, Publishing Solutions, Digital Transformation and Customer Support.

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Molecular Genetics and Metabolism | Journal | ScienceDirect.com by Elsevier
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morquiosity.com

morquiosity.com morquiosity.com           
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Morquio A is a form of mucopolysaccharidosis (MPS), a lysosomal storage disorder. Learn more about the symptoms, diagnostics and disease management strategies.

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Greenwood Genetic Center
Clinical genetic services, diagnostic laboratory testing, educational programs, and research in the field of medical genetics are all offered by the GGC in SC. . The Great Lakes Commission is a United States interstate agency established in 1955 through the Great Lakes Basin Compact, in order to "promote the orderly, integrated and comprehensive development, use and conservation of the water resources of the Great Lakes Basin," which includes the Saint Lawrence River. The Great Lakes Commission provides policy development, coordination, and advocacy on issues of regional concern, as well as communication and research services. The eight member states are Illinois, Indiana, Michigan, Minnesota, New York, Ohio, Pennsylvania, and Wisconsin. The Canadian provinces of Ontario and Quebec are associate members. Each state has three votes on matters coming before the commission, while associate members and observers (representing the United States and Canadian federal governments, tribes, and other regional organizations) are permitted to participate in discussions, deliberations and other activities as approved by the Commission but have no vote.There is a separate and distinct entity with a similar brief, the International Joint Commission, which exists between the federal levels of the United States and Canada.

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