A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene

por Vinagre-Aragón, Ana, Campo-Caballero, David, Mondragón-Rezola, Elisabet, Pardina-Vilella, Lara, Hernandez Eguiazu, Haizea, Gorostidi, Ana, Croitoru, Ioana, Bergareche, Alberto, Ruiz-Martinez, Javier
Publicado 2021

Defects of Nutrient Signaling and Autophagy in Neurodegeneration

por Ondaro, Jon, Hernandez-Eguiazu, Haizea, Garciandia-Arcelus, Maddi, Loera-Valencia, Raúl, Rodriguez-Gómez, Laura, Jiménez-Zúñiga, Andrés, Goikolea, Julen, Rodriguez-Rodriguez, Patricia, Ruiz-Martinez, Javier, Moreno, Fermín, Lopez de Munain, Adolfo, Holt, Ian James, Gil-Bea, Francisco Javier, Gereñu, Gorka
Publicado 2022

Elevated urine BMP phospholipids in LRRK2 and VPS35 mutation carriers with and without Parkinson’s disease

por Gomes, Sara, Garrido, Alicia, Tonelli, Francesca, Obiang, Donina, Tolosa, Eduardo, Martí, Maria José, Ruiz-Martínez, Javier, Vinagre-Aragón, Ana, Hernandez-Eguiazu, Haizea, Croitoru, Ioana, Marshall, Vicky L., Koenig, Theresa, Hotzy, Christoph, Hsieh, Frank, Sakalosh, Marianna, Tengstrand, Elizabeth, Padmanabhan, Shalini, Merchant, Kalpana, Bruecke, Christof, Pirker, Walter, Zimprich, Alexander, Sammler, Esther
Publicado 2023