Top 100 alternative sites to smsresearchfoundation.org
Supporting Families who have Children and Adults with Smith-Magenis Syndrome - Smith-Magenis Syndrome Foundation UK
Help us support a fulfilling future for everyone living with Smith-Magenis syndrome We want to bring more families together, provide education and awareness training, and sponsor research into SMS. But we can’t do it without your help. We are the Smith-Magenis Syndrome (SMS) Foundation UK, and we support families who have children and adults with …
Föreningen Smith-Magenis syndrom
Smith-Magenis Syndrome Australia |
Has your child or loved one recently been diagnosed with Smith-Magenis Syndrome (SMS)? Are you seeking local connection and support? SMS Australia is a local not-for-profit organisation which drives awareness, support and a sense of community; enhancing the lives of children with SMS, and their families.
PRISMS - Parents & Researchers Interested in Smith-Magenis Syndrome
PRISMS is dedicated to providing information and support to families of persons with SMS
Willkommen auf smith-magenis.at, der Webseite des Vereins Smith-Magenis-Syndrom Österreich - Smith-Magenis-Syndrom Österreich
Willkommen auf den Seiten des Vereins Smith-Magenis-Syndrom Österreich. Wir bieten eine Anlaufstelle für Betroffene und Interessierte bzw Fachpersonal rund um das Smith-Magenis-Syndrom in Österreich.
Author: Alexander Ströher
Norsk forening for Smith-Magenis syndrom
Norsk forening for Smith-Magenis syndrom arbeider for å spre informasjon og kunnskap om SMS syndrom til alle som ønsker det.
Startseite - Smith-Magenis-Syndrom CH
El síndrome de Smith Magenis – Síndrome Smith Magenis. Ayuda a familias.
¿Qué es el síndrome de Smith Magenis? No te pierdas ninguna de las publicaciones sobre
Sirius e.V. – Verein für Selbsthilfe, Information und Rat im Umgang mit dem Smith-Magenis-Syndrom
Stichting Smith Magenis syndroom Nederland
Stichting Smith Magenis syndroom Nederland is een samenwerkingsverband van ouders, familieleden, verzorgers en zorgprofessionals die zorgen voor of werken met kinderen of volwassenen met SMs
Smith Magenis Syndroom Belgie | SMsBE
Down Syndrome Research Foundation | DSRF UK
The DSRF UK Is A National Charity Formed By Parents Of Down’s Syndrome Children Who Want Greater Emphasis Placed On Medical Research.
Author: Down's Syndrome Research Foundation
The Cute Syndrome Foundation: SCN8A Epilepsy Support, Awareness, and Research - Home - The Cute Syndrome Foundation
Learn more about The Cute Syndrome Foundation and the SCN8A Epilepsy and PCDH19 Epilepsy Research we fund
Félag áhugafólks um Smith-Magenis heilkenni (SMS)
Talið er að 1 af hverjum 25.000 séu með sjúkdóminn en hann orsakast af litningagalla og hefur mörg alvarleg og víðtæk einkenni. Við tökum vel á móti öllum nýjum einstaklingum sem vilja taka þátt og starfa fyrir félagið. Félagið tekur með þökkum á móti öllum styrkjum stórum sem smáum.
Author: Admin
Global Down Syndrome Foundation | Research, Care, Education, Advocacy
The Global Down Syndrome Foundation is dedicated to improving the lives of people with Down syndrome through research, medical care, education and advocacy.
Angelman Syndrome Foundation | Welcome
Angelman Syndrome Foundation
Author: Angelman Syndrome Foundation
Irlen Syndrome Foundation
Visit the post for more.
Noonan Syndrome Foundation
The Noonan Syndrome Foundation: created to help support, educate, & advocate for and on behalf of all those who have bee affected by Noonan Syndrome.
Fragile X Syndrome Research & Treatment • FRAXA Research Foundation - Finding a Cure for Fragile X
FRAXA Research Foundation’s mission is to find effective treatments and ultimately a cure for Fragile X syndrome. Fragile X syndrome is the most common inherited cause of autism and intellectual disabilities We directly fund research grants and fellowships at top universities around the world. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments.
Author: Holly Roos
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Angelman syndrome Research
Jerome Lejeune Foundation USA - Down Syndrome Research, Care, and Advocacy
The Jerome Lejeune Foundation USA centers its activities on Research, Care, and Advocacy for people with Down Syndrome.
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CSRF - Cushing's Support & Research Foundation - Cushing's Syndrome Resources
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Welcome to Loeys-Dietz Syndrome Foundation Canada | Loeys-Dietz Syndrome Foundation Canada
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Home - Dravet Syndrome Foundation
Your Content Goes Here More News Dravet Syndrome Foundation is a non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form
Author: Admin
Shwachman-Diamond Syndrome Foundation
What is SDS? Shwachman Diamond Syndrome (SDS) is a rare blood disorder that affects the pancreas, bone marrow, and skeleton, but other organs may also be affected.
Loeys-Dietz Syndrome Foundation
Our purpose is to provide information about what Loeys-Dietz Syndrome is and give hope to those impacted by the condition. We hope that you will find medical information and personal support to assist you and your family on your journey with Loeys-Dietz Syndrome. Learn more about our foundation and
False Memory Syndrome Foundation
The False Memory Syndrome Foundation is a 501(c)(3) organization founded in March, 1992 to seek the reasons for the spread of the false memory syndrome, to work for ways to prevent the spread of the false memory syndrome, and to aid those who were affected by the false memory syndrome and bring their families into reconciliation.
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PFD Research Foundation | The Official Research Foundation of AUGS | PFD Research Foundation
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Bedford Research Foundation - Bedford Research Foundation
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Reye's Syndrome | National Reye's Syndrome Foundation | United States
In 1974, the National Reye's Syndrome Foundation, a children's health advocacy organization, was incorporated as a 501(c)3 charity, with a mission to eradicate the incidence of Reye's Syndrome. The Foundation does not receive, nor seek, government funding, and relies on the generosity of donors for support of all progr
Gould Syndrome - COL4A1 - COL4A2 genes - Gould Syndrome Foundation
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Joseph Smith Foundation | Remaining True to the Restoration - Joseph Smith Foundation
HOME | Sealy & Smith FoundationSealy & Smith Foundation
Just another WordPress site
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Utah Down Syndrome Foundation : Home
Author: John M Simmons
Mal de Débarquement, Debarkation Syndrome | MdDS Foundation
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| FAST (Foundation for Angelman Syndrome Therapeutics)
FAST España es una fundación, sin ánimo de lucro, creada por familias españolas con hijos afectados por el Síndrome de Angelman, con la finalidad de concienciar a la comunidad española y trabajar juntos por promover el desarrollo de terapias que propicien la cura y llevar el tratamiento a la práctica médica, actual, lo más rápido posible.
The National Fragile X Foundation | Fragile X Syndrome
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Home - Phelan-McDermid Syndrome Foundation
Improving lives affected by Phelan-McDermid Syndrome Join Donate Newly Diagnosed International DataHub Upcoming Events Resource Library It is the mission of the Phelan-McDermid Syndrome Foundation to improve the quality of life of those affected by Phelan-McDermid syndrome worldwide by providing family support, accelerating research, and raising awareness. Latest News & Blog Post We are Phamily […]
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The Alfred E. Smith Memorial Foundation
The Alfred E. Smith Memorial Foundation supports and aids the poor, sick, and underprivileged of the Archdiocese of New York, regardless of race, creed, or color.
Smith-Barbieri | A Charitable Foundation
The Kelvin and Eleanor Smith Foundation
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Rett Syndrome Research Trust: The Trusted Source for Rett Syndrome Information
Rett Syndrome Research Trust advances medical research, news and information about Rett Syndrome. A singular guide for parents and the scientific and medical community.
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