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Neuroscience Letters|December 22, 2020
Mini-Review: The MSA transcriptomeAlexandra Pérez-Soriano, María J Martí
Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2003
Pure akinesia: an unusual phenotype of Hallervorden-Spatz syndromeJosé L Molinuevo, María J Martí, Rafael Blesa, et al.
Archives of Neurology|February 16, 2005
A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndromeMario Ezquerra, Jaume Campdelacreu, Esteban Muñoz, et al.
General Hospital Psychiatry|December 27, 2005
Response to 4-month treatment with reboxetine in Parkinson's disease patients with a major depressive episodeLuis Pintor, Eva Baillès, Francesc Valldeoriola, et al.
Neurobiology of Aging|July 24, 2012
MAPT H1 haplotype is associated with enhanced α-synuclein deposition in dementia with Lewy bodiesMartí Colom-Cadena, Ellen Gelpi, María J Martí, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 2, 2009
Cerebrospinal tau, phospho-tau, and beta-amyloid and neuropsychological functions in Parkinson's diseaseYaroslau Compta, María J Martí, Naroa Ibarretxe-Bilbao, et al.
NPJ Parkinson'S Disease|December 2, 2021
Transcriptome analysis in LRRK2 and idiopathic Parkinson's disease at different glucose levelsRubén Fernández-Santiago, Anna Esteve-Codina, Manel Fernández, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2011
LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutationOswaldo Lorenzo-Betancor, Lluís Samaranch, Mario Ezquerra, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2022
Intermediate and Expanded HTT Alleles and the Risk for α-SynucleinopathiesSergio Pérez-Oliveira, Ignacio Álvarez, Irene Rosas, et al.
Brain : a Journal of Neurology|December 20, 2024
In-depth mass-spectrometry reveals phospho-RAB12 as a blood biomarker of G2019S LRRK2-driven Parkinson's diseaseAdriana Cortés, Toan K Phung, Lorena de Mena, et al.
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