Seminari Vall d’Hebron: Trastorns Lisosomals. Un focus en la malaltia de Fabry

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  Sala d'Actes de Pavelló Docent HUVH —
19/11/2018
19/11/2018 -- From 08:30h to 18:00h
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Vall d'Hebron Institut de Recerca (VHIR)
Modality: Presencial
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Programa Científic

8:30 Sessió inaugural 
9:00 Maneig clínic de la malaltia de Fabry. Moderadors: M. del Toro & G. Pintos-Morell
Miguel A. Torralba (Hospital Clínico, Zaragoza): Pathophysiology of Fabry disease: role of biomarkers and genetic variants
Alberto Ortiz (Fundación Jiménez Díaz, Madrid): Overview of consensus treatment and precission medicine approach in Fabry disease
James C. Moon (Barts Heart Centre, London, United Kingdom): Insights into early and advanced cardiomyopathy in Fabry disease from MRI
Michael West (Dalhousie University, Halifax, Canada): What have we learned after 10 years of Canadian Fabry Disease Initiative (CFDI)?
11:00  Cofee Break
11.30 Noves estratègies terapèutiques per les malalties lisosòmiques. Moderadors: N. Ventosa & S. Schwartz Jr.
Ibane Abasolo (CIBBIM-Nanomedicine): Nanomedicine in lysosomal disorders. Project  Smart4Fabry
Roberto Giugliani (Porto Alegre, Brazil): Fusion proteins and other strategies to cross the Blood-Brain-Barrier (BBB).
Michael West (Dalhousie University, Halifax, Canada). Gene therapy clinical trial for Fabry disease
Fàtima Bosch (CBATEG-UAB): Gene therapy approaches for Sanfilippo A and other lysosomal disorders
13:30 Discussió general
14:00 Lunch 

Fòrum obert a pacients i professionals
 
15:00 Situació actual del tractament per les malalties lisosòmiques.  Moderador: J. Torrent-Farnell
Vivències personals. Pacients, familiars i professionals de la sanitat conjuntament 
18:00 Resum final, missatges per emportar, i comiat. Guillem Pintos-Morell

Més Informació: smart4fabry@smart4fabry.eu  i  minoritaries_VH@vhebron.net

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