Showing results (211-220 of 358) with videos related to
Sort By:
Pageof 36
Frontiers in Cell and Developmental Biology|March 7, 2022
Bioimpedance Phase Angle as a Prognostic Tool in Late-Onset Pompe Disease: A Single-Centre Prospective Study With a 15-year Follow-UpSabrina Ravaglia, Rachele de Giuseppe, Annalisa Carlucci, et al.Neuromuscular Disorders : NMD|February 8, 2011
Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodiesHarriet P Lo, Enrico Bertini, Massimiliano Mirabella, et al.Translational Psychiatry|July 9, 2024
Serum dysregulation of serine and glycine metabolism as predictive biomarker for cognitive decline in frail elderly subjectsAlberto Imarisio, Isar Yahyavi, Clara Gasparri, et al.Journal of the Neurological Sciences|July 6, 2015
Protracted late infantile ceroid lipofuscinosis due to TPP1 mutations: Clinical, molecular and biochemical characterization in three sibsRaffaella Di Giacopo, Luciano Cianetti, Viviana Caputo, et al.American Journal of Medical Genetics. Part A|August 18, 2016
Cognitive, adaptive, and behavioral features in Joubert syndromeSara Bulgheroni, Stefano D'Arrigo, Sabrina Signorini, et al.Acta Neurologica Belgica|January 7, 2023
Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutationsGiovanna De Michele, Gianluigi Rosario Palmieri, Chiara Pane, et al.Jornal Brasileiro De Nefrologia|December 18, 2014
Smoking as risk factor for chronic kidney disease: systematic reviewUbiracé Fernando Elihimas Júnior, Helen Conceição dos Santos Elihimas, Victor Macedo Lemos, et al.Neurology|September 4, 2016
Impulsive-compulsive behaviors in parkin-associated Parkinson diseaseFrancesca Morgante, Alfonso Fasano, Monia Ginevrino, et al.Parkinsonism & Related Disorders|February 18, 2021
Genetic characterization of a cohort with familial parkinsonism and cognitive-behavioral syndrome: A Next Generation Sequencing studyMarina Picillo, Monia Ginevrino, Giovanna Dati, et al.Cerebellum (London, England)|September 10, 2013
Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease?Andrea Poretti, Martin Häusler, Arpad von Moers, et al.Pageof 36