Showing results (131-140 of 177) with videos related to
Sort By:
Pageof 18
Gastroenterology|August 25, 2015
Heritability of Hepatic Fibrosis and Steatosis Based on a Prospective Twin StudyRohit Loomba, Nicholas Schork, Chi-Hua Chen, et al.Current Pathobiology Reports|May 31, 2016
The role of IL-17 signaling in regulation of the liver-brain axis and intestinal permeability in Alcoholic Liver DiseaseHsiao-Yen Ma, Jun Xu, Xiao Liu, et al.Cerebrovascular Diseases (Basel, Switzerland)|September 14, 2013
Circulating markers of endothelial dysfunction and platelet activation in patients with severe symptomatic cerebral small vessel diseasePhilippa C Lavallée, Julien Labreuche, Dorothée Faille, et al.Ebiomedicine|September 20, 2025
Comparative analysis of cerebrospinal fluid neurofilament medium, light and heavy chain in neurodegenerative diseases using an in-house assay for the detection of neurofilament medium chainBadrieh Fazeli, Sara Botzenhardt, Franziska Bachhuber, et al.Neurology. Genetics|October 27, 2025
Neurofilament Light Chain as a Biomarker of Disease Progression in Lafora DiseaseLorenzo Muccioli, Bazile Ganceviciute, Felicitas Becker, et al.Neurological Research and Practice|June 27, 2020
Genotypes and phenotypes of patients with Lafora disease living in GermanyDavid Brenner, Tobias Baumgartner, Sarah von Spiczak, et al.Hepatology Communications|April 8, 2020
Primary Alcohol-Activated Human and Mouse Hepatic Stellate Cells Share Similarities in Gene-Expression ProfilesXiao Liu, Sara Brin Rosenthal, Nairika Meshgin, et al.Gastroenterology|December 3, 2016
Magnetic Resonance Elastography vs Transient Elastography in Detection of Fibrosis and Noninvasive Measurement of Steatosis in Patients With Biopsy-Proven Nonalcoholic Fatty Liver DiseaseCharlie C Park, Phirum Nguyen, Carolyn Hernandez, et al.Cellular and Molecular Life Sciences : CMLS|July 22, 2018
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALSAnika M Helferich, Sarah J Brockmann, Jörg Reinders, et al.Brain : a Journal of Neurology|December 11, 2025
Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosisÓscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, et al.Pageof 18