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Eduardo Fidel Tizzano

Institutions of which they are part

Head of group
Genetics Medicine
Vall Hebron Institut de Recerca

Eduardo Fidel Tizzano

Institutions of which they are part

Head of group
Genetics Medicine
Vall Hebron Institut de Recerca

Projects

Implementación de una base de datos genómicos del gen SMN2 en pacientes con AME para evaluar la eficacia terapéutica: Correlación genotipo-fenotipo

IP: Eduardo Fidel Tizzano
Collaborators: -
Funding agency: asociación GaliciAME
Funding: 20080.2
Reference: GALICIAME/BECA/2019/TIZZANO
Duration: 19/12/2019 - 18/09/2020

Aproximación genómica en atrofia muscular espinal (AME): estudio de casos especiales de pacientes con AME.5q y caracterización de pacientes con AME-no-5q.

IP: Eduardo Fidel Tizzano
Collaborators: -
Funding agency: Instituto de Salud Carlos III
Funding: 159720
Reference: PI18/00687
Duration: 01/01/2019 - 30/06/2023

Estudios funcionales de mutaciones del gen CFTR para establecer una terapia personalizada en pacientes con Fibrosis Quística

IP: Eduardo Fidel Tizzano
Collaborators: Paula Fernández Álvarez, SILVIA GARTNER TIZZANO
Funding agency: Fundación Invest. Médica Mutua Madrileña
Funding: 104213
Reference: MM/XIV/RECERCA/2017/TIZZANO
Duration: 10/10/2017 - 30/09/2021

Implementació de la Medicina Personalitzada basada en la Genòmica en Malalties Minoritàries Neurològiques no Diagnosticades

IP: Alfons Macaya Ruíz
Collaborators: Elena García Arumí, Francina Munell Casadesus, Teresa Vendrell Bayona, Ramon Martí Seves, Gómez Andrés, David, Eduardo Fidel Tizzano
Funding agency: Generalitat de Catalunya - Departament de Salut
Funding: 113977.67
Reference: SLT002/16/00174
Duration: 01/01/2017 - 31/12/2019

Related news

The results show that, in some patients with mutations in the X chromosome, the healthy gene is inactivated and the mutated gene manifests itself, which favors the onset of the disease.

On January 24, a session was held to explain what these three-dimensional models are and what advantages they have, as well as to review some of their applications in research.

The research has studied the structure and function of proteins related to this degenerative disease and their interaction with SMN2 messenger RNA (mRNA), which is key to the evolution of patients.

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