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Michelle`s website, Rett- Syndrom, Rett- Syndrome, Syndrome de Rett
Michelle`s site über das Rett- Syndrom
Author: Thorsten Schmidt
Homepage | International Rett Syndrome Foundation
Author: Kassie Morell; Mom; Kaylie age 4
Rett-Syndrom – Deutsche Rett-Syndrom Gemeinschaft
Syndrome de Rett
Le Syndrome de Rett est une maladie génétique rare provocant un grave désordre neurologique; un handicap mental associé à une infirmité motrice autrement dit : un polyhandicap.
Landsforeningen Rett Syndrom – En forening for Rett
Rett Research Australia – Rett Syndrome
Elternhilfe Rett-Syndrom
Entwicklungsstillstand und Verlust der Handfunktion können auf das Rett-Syndrom hinweisen. Diagnose Rett-Syndrom die Elternhilfe ist an deiner Seite.
Author: Rett Deutschland e V
Home | Rett Syndrome
Author: The Latest Information
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.
Rett Syndrome Society of British Columbia : Rett Syndrome Society of BC
Rett Syndrome Rett Syndrome is a unique developmental disorder impacting mainly females and begins to appear in early childhood. Symptoms can include regression in communication skills, motor skills and other health issues. Learn about Rett Syndrome Our Mission Our mission is to support, educate, and empower those that live with Rett Syndrome and their families. […]
ÖRSG – Österreichische Rett-Syndrom Gesellschaft – Selbsthilfegruppe für Familien mit Rett-Syndrom
"Der persönliche Austausch bei den Treffen mit den anderen Eltern ist für uns unheimlich wertvoll - für unseren Pflege-Alltag daheim mit unserer Rett-Tochter. Jeder hier gibt den Anderen Tipps und berichtet über erfolgreiche Therapien und praktische Hilfsmittel für den Alltag - eine große Rett-Familie!" (Markus M. - Vater einer 16jährigen Rett-Tochter) Helfen Sie uns helfen …
Ontario Rett Syndrome Association | O.R.S.A. – rett
Rett University - E-Learning Platform for Rett Syndrome
Linashoffnung – Ich habe das Rett-Syndrom und eine Hoffnung.
Same as U - Uppmärksammar Retts syndrom
Same As U är ett UF-företag från Linköping. Same As U vill uppmärksamma och bidra till ökad kunskap kring Retts Syndrom som är ett sällsynt syndrom som nästan endast drabbar flickor.
Unicorn Meadows Rett Syndrome
Rett syndrome and Related Disorders
In this Telethon Kids Institute subsite, our Rett syndrome research team manages a national and international database of Rett syndrome.
Rett Syndrome Europe – RSE
Unicorn Meadows Rett Syndrome
Other sites like rettsyndrome in
Ailinas Welt mit dem Rett-Syndrom
Rett-Syndrom-Elternhilfe - Start
Rett-Syndrom-Elternhilfe Landesverband Nord e.V.
Rett Syndrome Association of IrelandThe Rett Syndrome Association of Ireland | Just another WordPress site
The Rett Syndrome Association of Ireland. Rett Syndrome normally affect girls. Get information on these conditions and the supports available.
Raising a Hand for Rett | Music Greats Supporting Rett Syndrome
Fridas Hoffnung – Ich habe das Rett-Syndrom und eine Hoffnung.
No Description.
Author: Hkboss
Army of Us – We Fight Rett Syndrome
Romys Hoffnung – Ich habe das Rett-Syndrom und eine Hoffnung.
Klara helfen - Gemeinsam gegen Rett-Syndrom
Author: Die Werbemacher
Home - RETT Syndrome Association of Australia
Rett Syndrome Association of Australia
Author: Gary Grocott
Home | Rett Syndrom Deutschland e.V.
Startseite - Rett-Syndrom-Südwest e.V.
Wir sind ein gemeinnütziger Verein, der Eltern und Angehörige von Kindern und Erwachsenen mit Rett-Syndrom zusammenführt und unterstützt.
Miriams Hoffnung – Ich habe das Rett-Syndrom und eine Hoffnung.
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.
Association Française du syndrome de Rett – Une association dans l'action !
Une association dans l'action !
Velkommen til Rettsyndrom.no - Norsk Forening for Rett Syndrom
Rett Syndrom ( RS ) er en sjelden nevrologisk sykdom som inntil nå bare er beskrevet hos jenter. I Norge fikk den første jenta diagnosen RS i 1983 og i dag kjenner man til omlag 130 jenter/ kvinner med Rett syndrom i Norge. Norsk Forening for Rett Syndrom ble stiftet i 1987 og har bla.… Les mer »
L'association - Les rêves de Lucie : Association Syndrome de Rett
Association créée pour aider Lucie atteinte du syndrome de Rett.
Manitoba Rett Syndrome Association - Home Page
Rett Syndrome (RS) is a neurological disorder seen almost exclusively in females and found in a variety of racial and ethnic backgrounds. The cause of Rett Syndrome has been traced to a defective gene on the X chromosome called MeCP2.
Action for Angela – Reverse Rett Syndrome – Save Our Daughter
What else rettsyndrome.in alternative websites
Welcome to Loeys-Dietz Syndrome Foundation Canada | Loeys-Dietz Syndrome Foundation Canada
Central Pain Syndrome Foundation -
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.
Welcome « Stevens Johnson Syndrome Foundation
Stevens Johnson Syndrome Foundation
Barth Syndrome Foundation : Home
Kiwanis Down Syndrome Foundation
Foundation For Angelman Syndrome Therapeutics
Home - Williams Syndrome Foundation
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
Gould Syndrome Foundation a 501(c)3 Nonprofit, exists to provide hope and help to children and adults with the Ultra Rare Disease, Gould Syndrome; affecting COL4A1 and COL4A2 genes.
Author: Jselser
Syndrome de Rett - La Vie selon Noémie - La Vie selon Noémie
Le Syndrome de Rett est une maladie rare d'origine génétique qui provoque un polyhandicap. Association La Vie selon Noémie
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
Utah Down Syndrome Foundation : Home
Author: John M Simmons
Mal de Débarquement, Debarkation Syndrome | MdDS Foundation
Mal de Débarquement, Disembarkment or Debarkation Syndrome is a disorder that leaves patients with a constant feeling of movement, as if on a boat. The MdDS Foundation advocates for and seeks treatments to end the suffering from MdDS. Learn more!
Author: MdDS Foundation
| 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
The NFXF serves all those living with Fragile X, including awareness, research, and community for individuals and families at all stages of life.
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 […]
Other websites similar as rettsyndrome.in
Welcome to M S F A | Moebius Syndrome Foundation Africa (MSFA)
Proteus Syndrome Foundation - Support and Education
The Proteus Syndrome Foundation's goals are Supporting / Educating Families of individuals living with Proteus Syndrome, public education, research funding
Pallister-Killian Syndrome Foundation of Australia
Pallister-Killian Syndrome Foundation of Australia
Author: Catch Themes
Smith-Magenis Syndrome Research Foundation
Barth Syndrome Foundation of Canada - Home
Restless Legs Syndrome Foundation Blog
Support for those affected by restless legs syndrome (RLS). For more info visit www.rls.org.
Author: Restless Legs Syndrome Foundation
Indian Valley Foundation
The mission of IVF is to enhance academic excellence within the Indian Valley School District through support of educational opportunities not funded by traditional sources.
Author: Celuch Creative Imaging
Indian Development Foundation
Mission W2K (Waste to Knowledge) is designed to mobilize old Newspapers/ Books and support children studying in IDF Bal Gurukuls spread across India. Your generous support will also help in...
Indian Dog Foundation - Home
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Indian Renal Foundation
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