Showing results (21-30 of 28) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Pain|August 12, 2009
Functional and structural nerve fiber findings in heterozygote patients with Fabry diseaseAnette Torvin Møller, Flemming Winther Bach, Ulla Feldt-Rasmussen, et al.Journal of the Neurological Sciences|May 9, 2009
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegiaKirsten Svenstrup, Peter Bross, Pernille Koefoed, et al.Molecular and Cellular Neurosciences|January 1, 2018
Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease modelRegina Hertfelder Reynolds, Maria Hvidberg Petersen, Cecilie Wennemoes Willert, et al.Scandinavian Journal of Clinical and Laboratory Investigation|October 18, 2017
The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry diseaseLis Hasholt, Martin Ballegaard, Henning Bundgaard, et al.Human Molecular Genetics|September 28, 2013
p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtinDagmar E Ehrnhoefer, Niels H Skotte, Safia Ladha, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 19, 2020
Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B GeneSara Bech, Annemette Løkkegaard, Troels T Nielsen, et al.Brain : a Journal of Neurology|March 21, 2016
Seasonal difference in brain serotonin transporter binding predicts symptom severity in patients with seasonal affective disorderBrenda Mc Mahon, Sofie B Andersen, Martin K Madsen, et al.Annals of Clinical and Translational Neurology|October 31, 2014
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsyMai-Britt Mosbech, Anne S B Olsen, Ditte Neess, et al.Pageof 3