JORDI MAUR PEREZ TUR
ABCA1 polymorphisms and Alzheimer's disease
Variant rs764542666 in CR1 leading to NMD in familial Alzheimer's disease
Identificacion y caracterización de una nueva mutación en PGRN causante de DFT - duplicado
Identificacion y caracterización de una nueva mutación en PGRN causante de DFT
Development of a cellular model to study the role of CR1 in Alzheimer's disease
Evaluation of a novel variant in CR1 in patients with Alzheimer's disease
Revisiting theories to explain the increased kinase activity of LRRK2 p.G2019S mutation.
Evaluation of a novel variant in PRRT2 in patients with paroxysmal kinesigenic dyskinesia (PKD)
Development of a PCR-dot-blot method to detect C9orf72 expansions.
Evaluation of a novel mutation in patients with Primary lateral Sclerosis (PLS).
Alteration of the splicing forms of the 5¿-UTR of DJ-1 (PARK7) in SNPs related to Parkinson disease in Basque population
Genetic analysis of NFE2L2 related variability in Parkinson 's disease.
Transcriptional regulation of LRRK2 (PARK8)
Genetic studies of susceptibility factors for Parkinson 's disease.
Alteración del splicing de DJ-1 (PARK7): implicación en enfermedad de Parkinson
STRUCTURAL AND FUNCTIONAL IN SILICO ANALYSIS OF LRRK2 MISSENSE SUBSTITUTIONS
Analysis of GIGYF2 in Basque population, systematic review and bioinformatic analysis of Parkinson-related coding variants
In silico phylogenetic and structural analysis of PINK1
ANÁLISIS DE PARK16 EN PARKINSON FAMILIAR
In silico structural analysis of LRRK2 and effects of Parkinson-related mutations
In silico analysis of PINK1 Parkinson related kinase: phylogenetic and structural approaches
Análisis Bioinformátio de la filogenia de la familia LGI