afm-telethon.com
The French Muscular Dystrophy Association (AFM)AFM - is composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling illness: neuromuscular diseases
http://www.afm-telethon.com/
AFM - is composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling illness: neuromuscular diseases
http://www.afm-telethon.com/
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Association Francaise contre les myopathies
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Association Francaise contre les myopathies
1 rue de●●●●●●●●ationale
e●y , FR, 91000
FR
View this contact
Association Francaise contre les myopathies
1 rue de●●●●●●●●ationale
e●y , FR, 91000
FR
View this contact
Association Francaise contre les myopathies
1 rue de●●●●●●●●ationale
e●y , FR, 91000
FR
View this contact
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The French Muscular Dystrophy Association (AFM) | afm-telethon.com Reviews
https://afm-telethon.com
AFM - is composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling illness: neuromuscular diseases
afm-telethon.com
AFM-Telethon / About AFM-Téléthon / Organisation
http://www.afm-telethon.com/about-afm/organisation.html
About AFM-Téléthon. Results of previous grant programs. Information and care services. Trials and skills centers. My company wants to help. Therapeutic and social innovation programs. In order to achieve its missions. Relies on an alliance of competencies: the professionals who work for the association, thousands of volunteers who take part in the fight but also the patients and their families, who pilot the whole strategy. Learn more about the players. Learn more about the governance. Dr Federico MINGOZ...
The French Muscular Dystrophy Association (AFM-Téléthon)
http://www.afm-telethon.com/map.html
About AFM-Téléthon. Results of previous grant programs. Information and care services. Trials and skills centers. My company wants to help. Therapeutic and social innovation programs. Cure through innovation 2016 is now available online. Long term correction of hyperbilirubinemia in animal models of Crigler-Najjar syndrome after AAV vector-mediated liver gene transfer. Here are the faces of Telethon 2016. Innovative biotherapies: towards high-precision medicine. Follow all the news from Myology 2016!
AFM-Telethon / Support us! / My company wants to help / Therapeutic and social innovation programs
http://www.afm-telethon.com/support-us/my-company-wants-to-help/therapeutic-innovation-programs.html
About AFM-Téléthon. Results of previous grant programs. Information and care services. Trials and skills centers. My company wants to help. Therapeutic and social innovation programs. My company wants to help. Therapeutic and social innovation programs. Therapeutic and social innovation programs. Needs to find new financial resources. Genethon Bioprod, a unique center in the world. Helping research in many ways. Programs for social innovation and for family support. The “Cure through innovation&rdq...
AFM-Telethon / Support us! / My company wants to help
http://www.afm-telethon.com/support-us/my-company-wants-to-help.html
About AFM-Téléthon. Results of previous grant programs. Information and care services. Trials and skills centers. My company wants to help. Therapeutic and social innovation programs. My company wants to help. My company wants to help. Your company can also help the Telethon. And AFM-Téléthon. It is possible for you to make a donation, to organize events or to help during the Telethon. Therapeutic and social innovation programs. Cure through innovation 2016 is now available online. Dr Federico MINGOZZI, ...
AFM-Telethon / News / New gene therapy success in a rare disease
http://www.afm-telethon.com/news/new-gene-therapy-success-in-a-rare-disease.html
About AFM-Téléthon. Results of previous grant programs. Information and care services. Trials and skills centers. My company wants to help. Therapeutic and social innovation programs. New gene therapy success in a rare disease. New gene therapy success in a rare disease. Six children that were treated and followed for at least 9 months. Had their immune system restored and clinical condition improved. This work, which. Was published today in the Journal of the American Medical Association (JAMA), was.
TOTAL PAGES IN THIS WEBSITE
21
Our network | EspeRare Foundation
http://esperare.org/en/our-network
Skip to main content. Advancing treatments for rare diseases Together. Impact of our model. Cilengitide in a renal disease. Our Mission and Vision. EspeRare aims to pioneer a collaborative system that brings together key rare disease stakeholders to explore the therapeutic value of existing pharmacotherapies, ultimately filling the translation gap and advancing the R&D process. 14 chemin des Aulx. Laboratoire de la Sauvegarde. 480 avenue Ben Gourion. 69009 Lyon, France. How to support us.
Atlantic Gene Therapies - From bench to bedside
http://www.atlantic-gene-therapies.fr/en
From bench to bedside. Investigator of the month! The 20 meeting of the World Muscle Society. New publication in Molecular Therapy! All the latest news. Atlantic Gene Therapies develops gene therapy strategies for diseases affecting the retina. The muscles or the central nervous system. More than 70 collaborators are involved, from researching innovative concepts to setting up tools and production processes compatible with producing vectors. That are to be administered to Man.
eVision - Clients
http://www.evision.ca/clients.php
Custom Development - Turn-Key Solutions. McGill University Health Centre. Ontario Institute for Cancer Research. Québec Fund for Health Research. Saskatchewan Foundation for Health Research. Nova Scotia Health Research Council. Manitoba Health Research Council. Heart and Stroke Foundation of Canada. Michael Smith Foundation for Health Research. Multiple Sclerosis Society of Canada. Communications Security Establishment Canada. Canada Foundation for Innovation. Canada Border Services Agency (CBSA).
eVision - News and events
http://www.evision.ca/news.php
Custom Development - Turn-Key Solutions. EVision is pleased to announce we were awarded a mandate with the Department of National Defence (DND) and Shared Services (SSC) to revisit the architecture and design as well as implement end-to-end SCCM 2012 environment. This is a mandate won under the Proservices Procurement vehicle of PWGSC (Public Works and Government Services Canada). 01022015 - eReviews at MUHC-RI compliant with the new framework for multi site research studies. The provisions in the Framew...
The Company | Genosafe
http://www.genosafe.com/about-us
A full CRO and consulting company. Careers – Jobs. Professional and scientific associations. QC testing – Product characterization. Call or visit us. Careers – Jobs. Professional and scientific associations. GenoSafe is a full contract research and consulting organization which specializes in evaluating the quality, safety and efficacy of innovative biological products. We meet our clients’ specific needs by performing custom studies in strict compliance with regulatory requirements. Placing our clients ...
Useful links | RareConnect Support & Capacity Building
http://blog.rareconnect.org/resources/useful-links
Social media case studies. Updates to RareConnect.org. 8211; The portal for rare diseases and orphan drugs. 8211; Searchable database which provides patients, family members and the public with information about current ongoing clinical research studies. Provides information about diseases and their related support and advocacy networks. It began as a feature of Genetic Alliance’s website, and this expansion improves both navigation and the number of information sources included. Is a free database acces...
Plan du site | AFM-Téléthon
http://www.afm-telethon.fr/sitemap
Avant le Téléthon 2016. Concerné par la maladie. 01 69 47 11 78. Vous êtes ici :. Biothérapies et maladies fréquentes. Loi du 11 février 2005 : Quelles avancées? Le Téléthon des Français de l’étranger. Progrès de la recherche. Thérapie génique et maladies fréquentes. Comité de la charte. Fédération des maladies orphelines. Comment organiser une manifestation Téléthon. Charte de bonne conduite. Rapport Annuel et Financier. Feuilleter le rapport annuel et financier 2015. Consultez nos offres d'emploi.
Des collaborations en Europe et dans le monde | AFM-Téléthon
http://www.afm-telethon.fr/guerir/international-938
Avant le Téléthon 2016. Concerné par la maladie. 01 69 47 11 78. Vous êtes ici :. Faîtes un don en ligne. Javascript désactivé : calcul du coût réel impossible. C'est ce que vous coûtera ce don après les 66% de réduction d'impôt. Ligne directe donateurs : 0825 07 90 95 (0,15 TTC/min prix d’un appel local). Faites un don au 3637. Impulser des collaborations en Europe et dans le monde. Acteur-clé de la recherche internationale. Réseau européen pour le développement de traitements des maladies neuromusculai...
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Spectacles
L'art divers et vivant. Du grand show au spectacle intimiste. Des reprises ou des créations, de nombreux styles, des spectacles qui évoluent avec le temps et les personnes qui les composent. Depuis 1977, le Forum du Mouvement s’est constitué un catalogue varié.Ses spectacles s’adaptent à de nombreux publics et de nombreux lieux. La diversité des disciplines et des genres permet au Forum de sans cesse se renouveler. Il vit au rythme de la création artistique. Vani Comédie musicale de Christian Pagès.
Antifascistisk mobilisering
Sveriges ledande antifascistiska nätverk. Monday, May 08, 2006. Posted by AFM-Sverige at 3:55 AM. Saturday, April 29, 2006. Mahmoud Aldebe har rätt! Han kräver islamisk lag - i Sverige. Posted by AFM-Sverige at 4:48 AM. Thursday, April 20, 2006. Aktionen mot FHM genomförd. Som utlovat har AFM-Österåker nu genomfört en aktion mot tidningen FHM. Klockan 03:40 inatt smög sig aktivister fram till dörren för tidningens högkvarter och fäaste ett meddelande. Förhoppningsvis har dom nu lärt sig sin läxa, så ...
TEA HOUSE 青山フラワーマーケット
AOYAMA FLOWER MARKET TEA HOUSE. 南青山本店 Flower Wine Night 5/27(水) 5/30(土). 吉祥寺 シャクヤクを束ねる会 5/21 5/27 5/28. U30a2 u30c8 u30ec u5409 u7965 u5bfa u5e97. U6b66 u8535 u91ce u5e02 u5409 u7965 u5bfa u5357 u753a1-1-24. U8a73 u7d30 u306f u3053 u3061 u3089. U5357 u9752 u5c71 u672c u5e97. U6771 u4eac u90fd u6e2f u533a u5357 u9752 u5c715-1-2. U8a73 u7d30 u306f u3053 u3061 u3089. U8d64 u5742Biz u30bf u30ef u30fc u5e97. U6771 u4eac u90fd u6e2f u533a u8d64 u57425-3-1. U8a73 u7d30 u306f u3053 u3061 u3089.
Your partner for volumetric compensation on the CMM / machine tools / LaserTRACER | AfM Technology
Service Solutions ». Engineering Package ». Software Solutions ». Software solutions for the. AfM Technology offers you extensive software solutions in the range of the geometrical measuring technology and the optimisation of Product Development Process. PDP) Whether volumetric compensation, data conversion, Preprozezzoren, measuring programmes, transference programms, automations, as well as documentations and the comparison of CALYPSO - quality control plans. Significant increase of accuracy.
Ihr Partner für volumetrische Kompensation am KMG / WZM / LaserTRACER | AfM Technology
Engineering Paket ». Softwarelösungen für die geometrische Messtechnik. AfM Technology bietet Ihnen umfangreiche Softwarelösungen im Bereich der geometrischen Messtechnik und der Optimierung von Produktentstehungsprozessen (PEP). Ob volumetrische Kompensation, Datenkonvertierung, Preprozessoren, Messprogramme, Übertragungsprogramme, Automatisierungen, sowie Dokumentationen und der Vergleich von CALYPSO-Prüfplänen. Volumetrische Kompensation an KMG und WZM. 2007 - 2015 AfM Technology GmbH.
The French Muscular Dystrophy Association (AFM)
About AFM-Téléthon. Results of previous grant programs. My company wants to help. Therapeutic and social innovation programs. Information and care services. Trials and skills centers. Call for proposals 2015/2016. AFM-Telethon supports projects following Call for Proposals after review by its Scientific Council or by Committees of Experts. To develop treatments for rare diseases, AFM has taken an innovative route: using biotherapies based on our knowledge of genes and cells. Your company can help. French...
AFM-Téléthon - Innover pour guérir
Collectés grâce à vous. Concerné par la maladie. 01 69 47 11 78. Faites un don en ligne. Javascript désactivé : calcul du coût réel impossible. C'est ce que vous coûtera ce don après les 66% de réduction d'impôt. Ligne directe donateurs : 0825 07 90 95 (0,15 TTC/min). Faites un don au 3637. L’efficacité de la thérapie génique pour le syndrome de Wiskott-Aldrich, maladie génétique rare qui altère les défenses immunitaires, a été démontrée et six enfants traités ont vu leur système immunitaire rétabli.
Blog de afm-telethon22 - Blog de afm-telethon22 - Skyrock.com
Mot de passe :. J'ai oublié mon mot de passe. Je vous presentes ce blog destiné au téléthon et tous ceux qui y particper comme benevole, malade, parent et ami de malade, et chercheur. Bonne visite a vous tous. Mise à jour :. Abonne-toi à mon blog! Je vous presente mon blog sur le téléthon qui se passe en france. Le téléthon est tres important et il se bat pour guerrir les maladie rare, orpheline. Merci a vous tous et bonne visite. Ou poster avec :. Posté le jeudi 21 mai 2009 07:44. 3637, internet et CB s...
AFM-Téléthon en Ille-et-Vilaine
Vidéos & Photos. Journée des familles 2015. Des expériences de chez nous. Bienvenue sur le site AFM-Téléthon 35! Le site regroupe la délégation AFM. Et la Coordination Téléthon. Il a pour but de réunir les informations, de suivre les actualités, des manifestations, photos, vidéos. Il est en cours de construction, excusez-nous pour la gêne occasionnée. Un espace Organisateur sera ouvert à partir du mois de septembre. André Guyomard. Coordinateur Ille et Vilaine. Exiger une France accessible à tous! 8220;L...
Témoignages
Quelques échos de nos prestations. Attention le contact de la compagnie a changé. Impossible de faire disparaître la trace de l'ancien. Pour nous contacter tél à Christian Pagès. Au 06 08 98 92 84. Tous les amis de l'école supérieure du spectacle témoignent pour soutenir le centre de formation professionnelle. Vous pouvez vous joindre à eux et ainsi participer au grand livre qui sera envoyé à tous les centre d'information et dans toutes les ambassades, ainsi qu'aux théâtres et maisons de la culture.
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