Gaig Ventura, Carles (Date of defense: 2011-03-25)
Las mutaciones en el gen LRRK2, en especial la G2019S, parecen ser una causa relativamente frecuente de enfermedad de Parkinson (EP).Mutaciones en este gen se detectan en el 5-6% de los casos con EP ...
Gil Navarro, Silvia (Date of defense: 2013-09-26)
INTRODUCCIÓN: La actual clasificación de afasia primaria progresiva (APP) reconoce tres variantes clínicas principales: no-fluente/agramatical (APP-vnf), semántica (APP-vs) y logopénica (APP-vl). ...
Campabadal Delgado, Anna (Date of defense: 2020-09-08)
BACKGROUND: The present Doctoral Thesis is focused on Rapid-eye-movement (REM) sleep behavior disorder (RBD) and olfactory dysfunction as biomarkers of Synucleinopathies, such as Parkinson’s disease ...
Uribe Codesal, Carme (Date of defense: 2019-05-03)
BACKGROUND AND OBJECTIVES. Parkinson’s disease is a heterogenous neurodegenerative disorder. To characterize homogeneous groups of PD patients, PD phenotypes have been described based on clinical data ...
Garcia Diaz, Anna Isabel (Date of defense: 2018-02-16)
Parkinson’s disease is a common neurodegenerative disorder that manifests with a wide range of non-motor symptoms. Among them, cognitive impairment is present in a high proportion of patients, having a ...