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Neurobiology of Aging|October 28, 2018
UNC13A polymorphism contributes to frontotemporal disease in sporadic amyotrophic lateral sclerosisKaterina Placek, G Michael Baer, Lauren Elman, et al.
Respiratory Medicine|February 17, 2025
Longitudinal respiratory trajectories in motor neuron disease phenotypes: Multiparametric characterization and clinical managementPilar M Ferraro, Elena Mollar, Laura Melissari, et al.
Physical Review Letters|March 28, 2015
Observation of a multimode plasma response and its relationship to density pumpout and edge-localized mode suppressionC Paz-Soldan, R Nazikian, S R Haskey, et al.
Clinical Kidney Journal|May 18, 2026
Long-term citrate treatment in high-risk kidney stone formers is not associated with metabolic adverse effectsAlexander Ritter, Lea Bührer, Daniel G Fuster, et al.
Diabetologia|October 24, 2022
Intra-islet insulin synthesis defects are associated with endoplasmic reticulum stress and loss of beta cell identity in human diabetesNoemi Brusco, Guido Sebastiani, Gianfranco Di Giuseppe, et al.
American Journal of Human Genetics|May 19, 2022
Integration of rare expression outlier-associated variants improves polygenic risk predictionCraig Smail, Nicole M Ferraro, Qin Hui, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 21, 2017
TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisationLaura Pozzi, Fabiola Valenza, Lorena Mosca, et al.
Journal of Alzheimer'S Disease : JAD|November 26, 2024
Clinical and biological underpinnings of longitudinal atrophy pattern progression in Alzheimer's diseasePilar M Ferraro, Laura Filippi, Marta Ponzano, et al.
Physical Review Letters|August 9, 2014
Tokamak operation with safety factor q95 < 2 via control of MHD stabilityP Piovesan, J M Hanson, P Martin, et al.
Nature Genetics|March 5, 2021
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomicsMarc Jan Bonder, Craig Smail, Michael J Gloudemans, et al.
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