
ATAXIANS.ORG
AtaxiansWe Are Ataxians
http://www.ataxians.org/
We Are Ataxians
http://www.ataxians.org/
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Summit Solutions
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Summit Solutions
Andrew Johnson
2849 B●●●●●●y Road
Caz●●●via , New York, 13035-9743
US
View this contact
Summit Solutions
Andrew Johnson
2849 B●●●●●●y Road
Caz●●●via , New York, 13035-9743
US
View this contact
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Ataxians | ataxians.org Reviews
https://ataxians.org
We Are Ataxians
Fundraising
http://www.ataxians.org/ataxians/Fundraising
This is where you come in. FARA. Make it simple to donate to their organizations, and we strongly encourage everyone to do that, and to spread the word and get others to donate. If you donate to NAF or MDA be sure to indicate exactly where you'd like your donation to go. But how about doing more? FARA, NAF, and MDA are more than happy to help you organize your own fundraiser or to be part of an existing event.
Ataxians Membership Request
http://www.ataxians.org/ataxians/Members/RequestMembership.cfm
Use this form to request membership to www.ataxians.org. Information submitted here will only be used for sharing among members of this site. You will be able to share or hide any information you choose, and you will be able to change these settings and more at any time once you become a member. Spinocerebellar Ataxia Type 1. Spinocerebellar Ataxia Type 2. Spinocerebellar Ataxia Type 3/MJD. Spinocerebellar Ataxia Type 4. Spinocerebellar Ataxia Type 5. Spinocerebellar Ataxia Type 6. Episodic Ataxia Type 1.
Ataxia Links
http://www.ataxians.org/ataxians/links
You can find much more information about ataxia at the following places (selecting any of these links will open the site in a new browser window):. National Ataxia Foundation (NAF). Friedreich's Ataxia Research Alliance (FARA). Muscular Distrophy Association (MDA). Friedreich Ataxia Research Assocation - Australia. Friedreich's Ataxia Parents' Group (FAPG). International Network of Ataxia Friends (InterNAF). Help Friedreich's Ataxia in South Australia. If you would like a site added to this list.
About Ataxia
http://www.ataxians.org/ataxians/About
Ataxias are broken down into many different named diseases, such as Spinocerebellar Ataxia, Friedreich's Ataxia, and others. Some of the Ataxias are inherited recessively, some are inherited dominantly, and others appear sporadically. The symptoms and progression of the conditions vary among the different diseases and even among different family members with the same disease. Some symptoms associated with Ataxia:. Progressive loss of coordination (ataxia) in the arms and legs. We also have links.
Website Login
http://www.ataxians.org/ataxians/Members
Enter your email address and password to log in to the site. If you don't know your password. Not a member yet? Do you have ataxia?
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Ataxia Support | Place for open discussion and comments for members of the New England Ataxia Support Groups.
Place for open discussion and comments for members of the New England Ataxia Support Groups. Skip to primary content. Skip to secondary content. WELCOME TO OUR BLOG! History of the NE Support Groups. Boston Area Support Group. The Central Massachusetts Support Group. The Maine Support Group. The Rhode Island Ataxia Support Group. The New Hampshire Ataxia Support Group. Word of the Day – technophobia. June 16, 2015. Today’s word is technophobia. This word refers to the fear of the effects of technology.
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The Ataxia Group of Maine is a support group for individuals with Ataxia. The Ataxia Group of Maine is a support group for individuals with Ataxia, their families and friends. If you have or know of someone with Ataxia and would like more information, please email us at. For more information on Ataxia you can also visit:. The National Ataxia Foundation Http:/ www.ataxia.org.
Home | Ataxia MJD Research Project, Inc.
What is Ataxia MJD (Machado-Joseph Disease)? Ataxia MJD Research Project, Inc. The Ataxia MJD Research Project was founded in 1998 by Laura Denning to find a treatment or a cure to Machado-Joseph Disease SCA Type 3. By funding scientific research on this rare genetic disease. In 1998, the San Francisco Chronicle published an article. About our story and our organization. Please read the most recent research news. About Ataxia MJD Research Project. And take action. Please consider a donation.
Ataxia Net
Como participar do Grupo. ATAXIA PROVOCA DISTROFIA MUSCULAR? Integrante de: Informações Gerais. O que é distrofia muscular? O termo distrofia muscular Refere-se a um grupo de mais de 30 doenças gnéticas que causam fraqueza progressiva e degeneração dos músculos. Esqueléticos usados durante o movimento voluntário. Essas doenças variam em. Idade do aparecimento, gravidade e padrões dos músculos afetados. Todas as formas de distrofia. Ler a Matéria Completa. Compartilhar com o Pinterest. Links para esta pos...
Ataxians
There are many people with different forms of ataxia all around the world. This site is simply meant to help us all connect, through the map and with other information that our members choose to share. If you have ataxia we invite you to join the site! Simply fill out and submit the form on the membership request. Page We welcome you to explore this site to learn about others like you! If you are a newly-diagnosed patient or family member you should visit the NAF. Website, the FARA. Page of this site.
Ataxia Reign - A Vanguard guild on Tharridon
Welcome to the new home of Ataxia Reign! Ataxia Reign has a long history in MMO's going back to the beta days of Lineage 2 and continuing on into EQ2 and now it makes its reappearance in Vanguard: Saga of Heroes! Ataxia Reign is currently accepting recruits lvl 20 and above of all races, classes and play times. Special acceptions can be made if you already know someone in the guild and they will vouche for you, or for groups of people wishing to join us together. This Site is always evolving.
Associação Ataxia Rio
Asociación Gallega de Ataxias: Quiénes somos
La Asociación Galega de Ataxias - AGA-,. Es una Entidad sin ánimo de lucro, que agrupa a los afectados por la enfermedad rara. Familiares y demás personas sensibilizadas con el tema, en el ámbito territorial de Galicia. Desde estas líneas deseamos animaros a la participación activa de todos los afectados y/o familiares, ya que, es necesario aunar esfuerzos y levantar una única voz, que será más fuerte cuantos más seamos los que gritemos a la vez. En la UE,. Deben padecerla pocos pacientes.
ataxias
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Bienvenidos a Federación Andaluza de Asociaciones de Ataxias
Acceso de Usuarios / Intranet. Que son las Ataxias? Servicio de Atención Social. Bienvenidos a Federación Andaluza de Asociaciones de Ataxias. I ntervención en radio del Presidente. Antonio Navajas, Presidente de ACODA, intervino en el programa de radio "La Onda sin barreras" de Pilar Sanabria, el pasado 27 de febrero, donde expuso los programas y actividades que se están llevando a cabo desde la Asociación dirigidos a afectados/as y familiares de Córdoba y provincia. Enlaces de la noticia:. Os infromamo...