Neurological Disorders Programme
Neurological Disorders Programme: composed of 7 research groups from different fields, from clinical genetics, molecular genetics and molecular and cellular physiology, specialized in multiple rare neuromuscular and neurological disorders, both of genetic and acquired origin.
Rare diseases studied
- Muscular dystrophies
- Spinal muscular atrophy
- Charcot-Marie-Tooth neuropathy
- SMA
- Myasthenia gravis and congenital myasthenia
- Inflammatory myopathies
- Inherited and acquired ataxias
- Friedreich’s ataxia
- Enfermedad de Lafora y otras epilepsias genéticas raras
- Enfermedades peroxisomales
- Enfermedades neuroinmunológicas
Objectives
To investigate the biological and physiopathological foundations of rare neurological disorders, directing the collaborative knowledge generated in the laboratory and in the clinical-basic interface towards the development of diagnostic and therapeutic translational tools, and towards clinical research initiatives.
Research groups of the PdI
Main Researcher | Institution | Province | Details |
Dalmau Obrador, Josep |
Instituto de Investigaciones Biomédicas August Pi i Sunyer |
Barcelona |
|
Gallano Petit, Mª Pía |
Instituto de Investigacion del Hospital de la Santa Cruz y San Pablo |
Barcelona |
|
Gallardo Vigo, Eduard |
Instituto de Investigacion del Hospital de la Santa Cruz y San Pablo |
Barcelona |
|
Pallardó Calatayud, Federico |
Universidad de Valencia |
Valencia |
|
Sanz, Pascual |
Agencia Estatal Consejo Superior de Investigaciones Científicas |
Valencia |
|
Sevilla, Teresa |
Fundación para la Investigación del Hospital la Fe |
Valencia |
|
Contact
[email protected]