Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Robberecht

Showing results (591-600 of 651) with videos related to

Pageof 66
Sort By:
Nature Neuroscience|November 30, 2004
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALSErik Storkebaum, Diether Lambrechts, Mieke Dewerchin, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
Human Molecular Genetics|February 8, 2018
Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationAndre Bento-Abreu, Gunilla Jager, Bart Swinnen, et al.
Archives of Neurology|April 15, 2009
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromesFrans Brugman, Jan H Veldink, Hessel Franssen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
Brain : a Journal of Neurology|March 3, 2011
Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging studyMaaike M van der Graaff, Caroline A Sage, Matthan W A Caan, et al.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Pageof 66

Showing results (591-600 of 651) with videos related to

Sort By:
Pageof 66
Nature Neuroscience|November 30, 2004
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALSErik Storkebaum, Diether Lambrechts, Mieke Dewerchin, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
Human Molecular Genetics|February 8, 2018
Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationAndre Bento-Abreu, Gunilla Jager, Bart Swinnen, et al.
Archives of Neurology|April 15, 2009
Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromesFrans Brugman, Jan H Veldink, Hessel Franssen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypesJ C Schymick, Y Yang, P M Andersen, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Acta Neuropathologica Communications|November 12, 2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brainsJonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, et al.
Brain : a Journal of Neurology|March 3, 2011
Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging studyMaaike M van der Graaff, Caroline A Sage, Matthan W A Caan, et al.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Nature Genetics|May 4, 2004
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyOleg V Evgrafov, Irena Mersiyanova, Joy Irobi, et al.
Pageof 66