Results for rare disease research
@jetpack
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ryanfoundation.net
Rare Diseases Foundation - The Ryan Foundation
The Ryan Foundation for Rare Disease Research exists to help build the bridge to improved rare disease therapy, legislation, and support with particular attention to Mucopolysaccharidosis (MPS) and other Lysosomal Diseases, by funding specific science and
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researchrare.org
ResearchRare.org
Rare Disease Research , we are a non-profit organization supporting Rare Disease Research
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ryanfoundation.org
Rare Diseases Foundation - The Ryan Foundation
The Ryan Foundation for Rare Disease Research exists to help build the bridge to improved rare disease therapy, legislation, and support with particular attention to Mucopolysaccharidosis (MPS) and other Lysosomal Diseases, by funding specific science and
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addiandcassi.com
The Addi and Cassi Fund - Niemann Pick Type-C - Childhood Alzheimer's
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
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addi-cassi.com
The Addi and Cassi Fund - Niemann Pick Type-C - Childhood Alzheimer's
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
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addieandcassie.com
The Addi and Cassi Fund - Niemann Pick Type-C - Childhood Alzheimer's
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
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hughhempel.com
The Addi and Cassi Fund - Niemann Pick Type-C - Childhood Alzheimer's
Home of Addi & Cassi Hempel, twins with the rare and fatal disease call Niemann Pick Type-C sometimes referred to as "Childhood Alzheimer's". The most exhaustive collection of information and resources about research into this deadly c
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jacobscure.com
Canavan Disease | Jacob's Cure, A Fight Against Canavan Disease
Jacob's Cure is a non-profit organization funding research into treatments & cures for Canavan Disease, a rare genetic neurological disorder affecting children.
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valentine5k.com
Valentine Run Portland :: Home
Fanconi Anemia Research Fund. Fanconi anemia is a rare genetic life threatening disease which leads to bone marrow failure and cancers in children and young adults. Come and join us in an effort to fight Fanconi anemia, a life threatening genetic disease
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valentinerunportland.com
Valentine Run Portland :: Home
Fanconi Anemia Research Fund. Fanconi anemia is a rare genetic life threatening disease which leads to bone marrow failure and cancers in children and young adults. Come and join us in an effort to fight Fanconi anemia, a life threatening genetic disease
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jacobscure.net
Canavan Disease | Jacob's Cure, A Fight Against Canavan Disease
Jacob's Cure is a non-profit organization funding research into treatments & cures for Canavan Disease, a rare genetic neurological disorder affecting children.
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curedementia.org
CureDementia
A rare opportunity to align research assets to cure dementia by recognizing that Alzheimer’s Disease, Parkinson’s Disease, Frontotemporal Lobar Degeneration, Amyotrophic Lateral Sclerosis, and Vascular Dementia are all part of the same problem.
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fairwayfestforelife.org
NW Alliance for Life - Official Website
We are seeking your support to find a cure for liver disease through research. Our focus is on rare liver disease with no cure. Primary Sclerosing Cholangitis (PSC) is a rare autoimmune disease that effects the bile ducts within the liver. It leads to
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go-ipad.org
.::.PKU Information.::.
The National PKU News web site provides news and information about phenylketonuria, a rare, inherited metabolic disease. Web site sections include: About PKU, PKU Support Information, Diet-Related information, PKU Research, and PKU Legislation and Policy.
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helpaidangetwell.org
Help Aidan Get Well
Help Aidan Get Well is a non-profit 501 (c) (3) organization bringing awareness to a rare incurable disease Hypophosphatasia. Our purpose is to raise money for research and education to find a treatment
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jacobscure.org
Canavan Disease | Jacob's Cure, A Fight Against Canavan Disease
Jacob's Cure is a non-profit organization funding research into treatments & cures for Canavan Disease, a rare genetic neurological disorder affecting children.
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jmmbush.org
index
This Foundation helps children with major medical problems afford medical bills so they can get treatment and hope for a brighter tomorrow. We also help fund research for a rare autoimmune disease, Juvenile Dermatomyositis that has attacked Jon's neice,
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mhe-hme.org
MHE Research Foundation~Multiple Hereditary Exostoses~Multiple Osteochondroma
MHE Research Foundation 501(c)(3) organization dedicated to finding a cure for this rare bone disease. Providing comprehensive information on Research, Orthopaedics, Genetics, Chronic Pain, Conferences and Doctor Directories to help locate medical care.
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mheresearchfoundation.org
MHE Research Foundation~Multiple Hereditary Exostoses~Multiple Osteochondroma
MHE Research Foundation 501(c)(3) organization dedicated to finding a cure for this rare bone disease. Providing comprehensive information on Research, Orthopaedics, Genetics, Chronic Pain, Conferences and Doctor Directories to help locate medical care.
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pkunews.org
National PKU News
The National PKU News web site provides news and information about phenylketonuria, a rare, inherited metabolic disease. Web site sections include: About PKU, PKU Support Information, Diet-Related information, PKU Research, and PKU Legislation and Policy
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wstfcure.org
wstfcure.org
Worldwide Syringomyelia Task Force Inc. is a nonprofit corporation that is based in Georgia. Our purpose is to educate the world about this rare disease and provide those affected with hope by advocating research for a cure; assisting those affected by p
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researchmatch.org
Welcome to ResearchMatch!
ResearchMatch is a not-for-profit effort that brings together researchers and people who are willing to learn more about research studies in a secure and convenient manner.
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csl.com
CSL Limited is a global biotherapy industry leader.
CSL Limited is a global, specialty biopharmaceutical company that researches, develops, manufactures and markets products to treat and prevent serious human medical conditions
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niemann-pickdisease.com
Niemann-Pick Disease | A Rare Fatal Lysosomal Storage Disease
Niemann-Pick disease is an inherited condition involving lipid metabolism, which is the breakdown, transport, and use of fats and cholesterol in the body. In
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alburx.com
CSL Limited is a global biotherapy industry leader.
CSL Limited is a global, specialty biopharmaceutical company that researches, develops, manufactures and markets products to treat and prevent serious human medical conditions
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cutislaxa.com
CUTIS LAXA INTERNATIONALE
Page d'accueil
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guthyjacksonfoundation.com
The Guthy-Jackson Charitable Foundation - Learn About NMO
The Guthy-Jackson Charitable Foundation funds research to find answers to the prevention, clinical treatment programs and a potential cure for NMO (Neuromyelitis Optica).
