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Move To A Cure. A Cure To Move. Receive regular updates on research and fundraising with the FSHD Canada Foundation. The singular goal of the FSHD Canada Foundation is to help find a cure — as soon as possible — for Canadians who suffer with FSHD. Latest News View All News. A Rare Person - A Documentary. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. We are excited to announce th...

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Move To A Cure. A Cure To Move. Receive regular updates on research and fundraising with the FSHD Canada Foundation. The singular goal of the FSHD Canada Foundation is to help find a cure — as soon as possible — for Canadians who suffer with FSHD. Latest News View All News. A Rare Person - A Documentary. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. We are excited to announce th...

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1 fshd

2 about the foundation

3 our story

4 our mission

5 our team

6 what is fshd

7 overview

8 types of fshd

9 incidence of fshd

10 other medical terms

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fshd,about the foundation,our story,our mission,our team,what is fshd,overview,types of fshd,incidence of fshd,other medical terms,genetics of fshd,genetic counselling,resources,research overview,funded research,faq's,get involved,donate now,latest news

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Home | fshd.ca Reviews

https://fshd.ca

Move To A Cure. A Cure To Move. Receive regular updates on research and fundraising with the FSHD Canada Foundation. The singular goal of the FSHD Canada Foundation is to help find a cure — as soon as possible — for Canadians who suffer with FSHD. Latest News View All News. A Rare Person - A Documentary. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. We are excited to announce th...

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fshd.ca

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Personal Campaigns

http://www.fshd.ca/personal-campaigns

2016 Bike for FSHD. Jennie and Nick Cherniwchan India - Mumbai to Goa. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. Much of what we know about DUX4 and its associated toxicity comes from cultured cells from FSHD patients. We basically take. FSHD Canada and the FSH Society are jointly funding a project called "Exploiting Genome Editing Technologies," led by.

2

Donate

http://www.fshd.ca/donate

Donate to FSHD Research. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. Much of what we know about DUX4 and its associated toxicity comes from cultured cells from FSHD patients. We basically take. FSHD Canada and the FSH Society are jointly funding a project called "Exploiting Genome Editing Technologies," led by. Friends of FSH Research. FSHD Global Research Foundation.

3

Genetics of FSHD

http://www.fshd.ca/overview/genetics-of-fshd

Both types of FSHD are autosomal dominant genetic disorders. Each child of a parent with FSHD has a 50% chance of inheriting FSHD. The type of FSHD inherited by the child is always the same as that of the affected parent (i.e. if the parent has FSHD1A, each child is at 50% risk for FSHD1A). The severity of the symptoms may differ from person to person within a family. Much of what we know about DUX4 and its associated toxicity comes from cultured cells from FSHD patients. We basically take.

4

Incidence of FSHD

http://www.fshd.ca/overview/incidence-of-fshd

The most common form of FSHD by far is FSHD type 1A (chromosome 4-linked FSHD). A conservative estimate of incidence is 1 in 14,000 births throughout the world; however, due to increased experience with FSHD, population-based research and improved genetic testing, this estimate may be low; actual incidence may be 1 in 7,500. Infantile FSHD (IFSHD) is characterized by onset in early childhood. There is no generally accepted estimate of its incidence, but it is rare. Friends of FSH Research.

5

Featured

http://www.fshd.ca/featured

Merry Christmas Jonas And Me Too! My contact information is posted on the FSHD Canada Foundation website so I get a lot of emails. Most are from Canadians but not all. Just before Christmas I got an email from Jonas in the Philippines. Jonas has FSHD. He’s about my age but in much worse shape. He can’t walk and relies on his scooter to get around. Two years ago a typhoon hit Jonas’ island. Jonas and his family survived but the scooter was badly damaged. Craig's Song - Who Turned Up Gravity? That is just ...

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en.wikipedia.org

Muscular dystrophy - Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Muscular_dystrophy

From Wikipedia, the free encyclopedia. In affected muscle (right), the tissue becomes disorganized and the concentration of dystrophin. Green) is greatly reduced, compared to normal muscle (left). Classification and external resources. Is a group of muscle diseases. That weaken the musculoskeletal. System and hamper locomotion (walking or moving). Muscular dystrophies are characterized by progressive skeletal muscle. Weakness, defects in muscle proteins. And the death of muscle cells. And the different m...

fshdchampions.org

FSHD Canada Foundation | FSHD Champions

https://fshdchampions.org/about/fshd-canada-foundation

An international alliance supporting Facioscapulohumeral Muscular Dystrophy research. Skip to primary content. Friends of FSH Research. Muscular Dystrophy Association (MDA). Muscular Dystrophy Campaign UK. US National Institutes of Health (NIH). Suite 201, 1100 1st Street SE. Calgary, Alberta T2G 1B1. Phone: 403.470.0141. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). Notify me of new comments via email.

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OTHER SITES

fshd-group.eu

Amis FSH Europe

Titre du site : Amis FSH Europe. Description : L'objectif principal de l'association est de rompre l'isolement des familles et de partager des informations sur la FSH. L'outil majeur de communication est notre site communautaire Internet.

fshd-group.fr

AMIS FSH

Pour accéder au menu privé. ADHERER Agissons pour guérir. Notre vue de la recherche. Présentation Vidéos Yegor VASSETZKY. La Gazette été 2015 est arrivée! 24/25 octobre 2015 à AGDE - WE et AG AMIS FSH. 26/27 NOVEMBRE 2015 à Montpellier - RARE 2015 - L'événement de référence nationale sur les maladies rares. Venez rencontrer les entreprises, c. Mercredi 3/jeudi 4/vendredi 5 JUIN - AUTONOMIC SUD - à LYON (EUREXPO). 6 août 2015 Donnez votre avis sur la MDPH. Victime d’un accident médical? Le Conseil des min...

fshd-registry.org

Facioscapulohumeral Muscular Dystrophy - UK Patient Registry for FSHD

UK Patient Registry for FSHD. UK FSHD Patient Registry. To help advance the research and development of treatment, therapies and care for all those diagnosed with FSHD. More information for particpants and their families. More infomormation for professional users. There are currently 885 patients registered in this database. The registry is funded by Muscular Dystrophy UK. With support from the John Walton Muscular Dystrophy Research Centre. And MRC Centre for Neuromuscular Disease.

fshd-selbsthilfe.de

FSHD-Selbsthilfe Berlin

fshd-selbsthilfe.net

fshd-selbsthilfe.net - This website is for sale! - fshd-selbsthilfe Resources and Information.

fshd.ca

Home

Move To A Cure. A Cure To Move. Receive regular updates on research and fundraising with the FSHD Canada Foundation. The singular goal of the FSHD Canada Foundation is to help find a cure — as soon as possible — for Canadians who suffer with FSHD. Latest News View All News. A Rare Person - A Documentary. A Rare Person is a series of short documentaries that aim to provide greater awareness as to how people cope with the impacts of a rare disease. Although these diseases are. We are excited to announce th...

fshd.cn

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fshd.fr

Observatoire National Français des patients atteints de DMFSH

Société Française de Myologie. Blog du groupe FSH de l'AFM. Registre italien de la FSH. Site de la FSH Society. Site de l'université de Rochester. Bienvenue sur le site de l'Observatoire National Français des patients atteints de DMFSH. Que vous soyez médecin ou personne atteinte de DMFSH, vous pouvez participer à cet Observatoire et ainsi aider la recherche. Ajout de nouvelles publications sur la DMFSH. La newsletter n 3 de Juin 2016 est arrivée. Questionnaire d'évaluation de notre site.

fshd.it

Home - FSHD

A National Italian Registry for FSHD. Deambulazione (punte e talloni). A National Italian Registry for Facioscapulohumeral Muscular Dystrophy (FSHD). Proudly powered by WordPress. Theme: Radiate by ThemeGrill.

fshd.managed133.serverclienti.com

Home - FSHD

A National Italian Registry for FSHD. Deambulazione (punte e talloni). A National Italian Registry for Facioscapulohumeral Muscular Dystrophy (FSHD). Venerdì 18 settembre, 2015. La variabilità fenotipica nella distrofia muscolare facioscapolomerale: training all’utilizzo di una nuova classificazione clinica. Sabato 19 settembre, 2015. Proudly powered by WordPress. Theme: Radiate by ThemeGrill. Per saperne di più.

fshd.net

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上午 8 00 11 30. 抚松县民政局婚姻登记处以下简称登记处于2004年初经县编委批复成立，2004年6月1日正式揭牌办公。登记处的主要职责是一办理婚姻登记二补发婚姻证三出具婚姻登记记录证明四撤销受协迫的婚姻五宣传婚姻法律法规，倡导文明婚俗。实行婚姻登记工作集中、规范管理是抚松县民政局落实新婚姻登记条例的重要举措。