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En nuestro foro podrás debatir diversos temas de interés sobre Epilepsia Rosa y enfermedades afines. Conoce las historias reales de nuestras niñas. Enlaces de interés.
http://www.pcdh19.net/
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En nuestro foro podrás debatir diversos temas de interés sobre Epilepsia Rosa y enfermedades afines. Conoce las historias reales de nuestras niñas. Enlaces de interés.
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PCDH19 Alliance - PCDH19 Epilepsy:19 Days for PCDH19 Matching Grant
PCDH19 Epilepsy:19 Days for PCDH19 Matching Grant. PCDH19 Alliance - PCDH19 Epilepsy:19 Days for PCDH19 Matching Grant. PCDH19 Epilepsy:19 Days for PCDH19 Matching Grant. A Cure is out there, wont you help us find it? From March 26th Through April 13th all Donations Will be Doubled. Your generous donation will help us continue to invest in medical research, raise awareness, increase proper diagnosis and raise hope for the Brave Children living with PCDH19 Epilepsy. 1 Make a Donation. Maegans fundraiser f...
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En nuestro foro podrás debatir diversos temas de interés sobre Epilepsia Rosa y enfermedades afines. Conoce las historias reales de nuestras niñas. Enlaces de interés.
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World Conference on PCDH19 - 3rd Edition
World Conference on PCDH19 - 3rd Edition. The third edition of the World. Will take place in Rome on 23 and 24 October 2015. Scientific research status and. This website contains the event agenda, speakers' names and bios, the abstract of every speech and, as soon as they'll be available, the conference videos. This Conference has been organised and will be hold by the nonprofit association ". Together for the research on PCDH19 " (. ONLUS INSIEME PER LA RICERCA PCDH19. Via A Poliziano, 8.
Mutation PCDH19 France
Journée Pique-nique PCDH19. Brève janvier 2016. Retrouver la brève du mois de janvier avec toutes les dernières actualités de l'association. Congrès de Neurologie Pédiatrique de Lille. Du 20 au 22 Janvier l'association PCDH19 France sera présente au Congrès de Neurologie Pédiatrique de Lille. Base de données Genida. Ce registre permet de collecter des données sur des individus atteints de maladies génétiques rares de façon confidentielle. Permanence Téléphonique. VAN Makline HOAREAU Sandra.
pcdh19info
Newly Diagnosed with PCDH19 Epilepsy. Call for abstracts for 2016 symposium. PCDH19 Alliance November Fundraiser. Shop the Alliance Store. Rock N' Roll Marathon Series- Be a PCDH19 Alliance Hero. American Epilepsy Society 2013. 2014 Professional and Family Symposium. The PCDH19 Alliance Welcomes you. Our mission is to improve the lives of children and families who are affected by PCDH19 Epilepsy. PCDH19 Epilepsy Professional and Family Symposium. More details coming soon. About the PCDH19 Alliance Video.
Insieme per la Ricerca PCDH19 – ONLUS – Insieme per la Ricerca PCDH19 – ONLUS
Fai una donazione tramite PayPal:. O dona il 5 x 1000. Insieme per la Ricerca PCDH19 ONLUS. Diventa un’azienda solidale. News & Iniziative. WE ARE PLEASED TO ANNOUNCE THE THIRD EDITION OF THE WORLD CONFERENCE ON PCDH19, ORGANIZED BY INSIEME PER LA RICERCA PCDH19 THE CONFERENCE WILL BE HELD IN ROME ON OCTOBER 24TH 2015. ABSTRACTS OF THE SPEECHES AND MORE DETAILS WILL BE AVAILABLE SOON. Know and fight this rare genetic disease. Improve the quality of life of affected children. In case of mutation, prothoca...
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