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Journal of Molecular Neuroscience : MN|May 26, 2017
Plasma and White Blood Cells Show Different miRNA Expression Profiles in Parkinson's DiseaseChristine Schwienbacher, Luisa Foco, Anne Picard, et al.Stem Cell Research|August 3, 2023
Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutationGiada Cattelan, Laura Sophie Frommelt, Chiara Volani, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2006
Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolateFlorian D Vogl, Irene Pichler, Susanna Adel, et al.Plos One|April 10, 2019
Effects of smoking status, history and intensity on heart rate variability in the general population: The CHRIS studyFederico Murgia, Roberto Melotti, Luisa Foco, et al.Journal of Psychiatric Research|December 5, 2012
Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics studyAyşe Demirkan, Aaron Isaacs, Peter Ugocsai, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.NPJ Parkinson'S Disease|April 18, 2023
Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriersMaria Paulina Castelo Rueda, Alessandra Zanon, Valentina Gilmozzi, et al.American Journal of Human Genetics|November 22, 2002
Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystoniaBirgitt Müller, Katja Hedrich, Norman Kock, et al.Neurology|January 18, 2015
Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PDAlice Serafin, Luisa Foco, Stefano Zanigni, et al.Parkinsonism & Related Disorders|April 25, 2021
Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controlsJannik Prasuhn, Max Borsche, Andrew A Hicks, et al.Pageof 28