Similar sites like 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

Categories: Business, Charitable Organizations
Topics: fundraising sanfiliippo, lysosomal disease, mps, mps iii, rare diseases, sanfilippo

teamsanfilippo.org Reviews

Sites similar to teamsanfilippo.org - Top 31 teamsanfilippo.org alternatives

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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phoenixnestbiotech.com
Phoenix Nest Inc.
Phoenix Nest Inc.

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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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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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abbygracefoundation.org
Abby Grace Foundation - Helping Find a Cure for Sanfilippo Syndrome
Helping Find a Cure for Sanfilippo Syndrome

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claritypharma.com
Clarity Pharma Research LLC - Pharmaceutical Market Research Companies, Pharmaceutical Market Research Reports, Rare Diseases
We provide custom pharmaceutical market research pre/post launch: market sizing, product uptake, treatment patterns, clinical utility, publication/presentation.

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parseghian.org
Niemann- Pick Disease - Ara Parseghian Medical Research Foundation - Lysosomal Disease
The Ara Parseghian Medical Research Foundation's goal is to find a cure for the devastating Niemann-Pick Type C disease.

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jerinicares.com
JeriniCares | HAE | hereditary angioedema | rare diseases
JeriniCares is a free support program created to assist HAE patients and their caregivers in navigating the current healthcare system with regard to reimbursement. JeriniCares provides comprehensive assistance for insurance-related issues. JeriniCares, HAE patients and HCP's potential sponsored clinical trials.

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shmediations.com
Sanfilippo & Haddad, LLP - Certified Mediators in Sacramento
Sanfilippo & Haddad offers mediation services in Northern California (Sacramento). We mediate workplace, contract, family, and personal injury disputes.

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atlantichc.com
GI therapeutics | Rare Diseases | Atlantic Healthcare
We are a specialist pharmaceutical company focused on developing & commercializing therapeutics that address unmet patient needs & rare diseases.

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geneticalliance.org.au
Genetic Support | Rare Diseases | Genetic Alliance Australia | Support for those affected directly or indirectly by genetic conditions so rare there is no support group
Support for those affected directly or indirectly by genetic conditions/rare diseases throughout Australasia. Information, support network, personal stories, news and events.

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nipd.com
Genetic testing for Cancer, Rare diseases & Reproductive health | Medicover Genetics
Extensive genetic testing portfolio to help healthcare professionals identify the most appropriate genetic test for the patients. Place genetics at the core of medical decisions!

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orsinihealthcare.com
Specialty Pharmacy | Rare Diseases | Gene Therapies
Orsini Specialty Pharmacy is the leading specialty pharmacy for rare diseases and gene therapies dedicated to providing exceptional care to patients.

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orsinispecialtypharmacy.com
Specialty Pharmacy | Rare Diseases | Gene Therapies
Orsini Specialty Pharmacy is the leading specialty pharmacy for rare diseases and gene therapies dedicated to providing exceptional care to patients.

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plexa.ai
Plexa - Find, Share & Discuss trusted content on Cancer & Rare Diseases
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onthepulseconsultancy.com
On The Pulse Consultancy | Expert Patient Insight | Rare Diseases
Independent consultancy partnering with global healthcare providers to drive patient education & choice in haemophilia & rare diseases.

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rarediseases.about.com
Rare Diseases
It may seem unfair to be diagnosed with a rare disease, but learning as much as you can will help you cope with your illness.

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raremark.com
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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mpssociety.org
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.

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sanfilippofoundation.org
The Sanfilippo Foundation - Place de la Musique
The Sanfilippo

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Categories: Computers/Internet/Web Design and Development, Regional/North America, Arts/Architecture, Non-Profit/Advocacy/NGO, Business

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jlksanfilippofoundation.com
JLK Sanfilippo Research Foundation
Creating an awareness of Sanfilippo Syndrome and to raise funds to find a cure for this rare genetic disease.

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sanfilipponews.com
Sanfilippo News Home | Sanfilippo Syndrome News
The Web's Daily Resource for Sanfilippo Syndrome News

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curesanfilippofoundation.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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stopsanfilippo.org
Fundación Stop Sanfilippo | Ayúdanos a parar la enfermedad
Stop Sanfilippo es una organización dedicada al fomento de la investigación contra el Síndrome de Sanfilippo y a la atención de los niños afectados

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alifeforelisa.org
A life For Elisa
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treatable-id.org
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116 inborn errors of metabolism related to intelectual disability that are treatable. With this tool clinician and scientist can make a diagnosis

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pediatricbrainfoundation.org
The Pediatric Brain Foundation - pediatricbrainfoundation.org
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lysogene.com
Home - Lysogene
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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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syndromepictures.com
Syndrome Pictures
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