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Journal of Inherited Metabolic Disease|April 19, 2011
Juvenile neuronal ceroid lipofuscinosis: clinical course and genetic studies in Spanish patientsMaría-Socorro Pérez-Poyato, Montserrat Milà Recansens, Isidre Ferrer Abizanda, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2019
RNA editing alterations define manifestation of prion diseasesEirini Kanata, Franc Llorens, Dimitra Dafou, et al.
Spanish Journal of Psychiatry and Mental Health|July 11, 2024
Altered activation of the dorsal anterior cingulate cortex during oddball performance in individuals at risk for Alzheimer's diseasePamela Chavarría-Elizondo, Carla Del Río-Torné, Pablo Maturana-Quijada, et al.
Acta Neuropathologica|December 11, 2012
Distinct patterns of APP processing in the CNS in autosomal-dominant and sporadic Alzheimer diseaseMarta Pera, Daniel Alcolea, Raquel Sánchez-Valle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 7, 2013
Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutationMarc Suárez-Calvet, Oriol Dols-Icardo, Albert Lladó, et al.
JCI Insight|February 8, 2024
Blocking IL-6 signaling prevents astrocyte-induced neurodegeneration in an iPSC-based model of Parkinson's diseaseMeritxell Pons-Espinal, Lucas Blasco-Agell, Irene Fernandez-Carasa, et al.
Neuropathology and Applied Neurobiology|March 17, 2021
Atypical astroglial pTDP-43 pathology in astroglial predominant tauopathyEllen Gelpi, Iban Aldecoa, Dolores Lopez-Villegas, et al.
Biomolecules|February 16, 2020
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob DiseaseFranc Llorens, Anna Villar-Piqué, Peter Hermann, et al.
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