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

G Querin

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Revue Neurologique|May 6, 2017
Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapyG Querin, G Sorarù, P-F Pradat
European Journal of Neurology|October 24, 2018
Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian regionC Bertolin, G Querin, I Martinelli, et al.
Revue Neurologique|November 15, 2024
Quantitative spinal cord imaging: Early ALS diagnosis and monitoring of disease progressionM Khamaysa, M El Mendili, V Marchand, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 29, 2017
The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA caseG Querin, I Martinelli, C Bertolin, et al.
Revue Neurologique|June 6, 2017
Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variantG Querin, P Corcia, T Lenglet, et al.
European Journal of Neurology|September 12, 2014
The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case reportG Querin, C Bertolin, A Martinuzzi, et al.
European Journal of Neurology|June 7, 2017
Spinal cord multi-parametric magnetic resonance imaging for survival prediction in amyotrophic lateral sclerosisG Querin, M M El Mendili, T Lenglet, et al.
European Journal of Neurology|February 22, 2018
New FIG4 gene mutations causing aggressive ALSC Bertolin, G Querin, V Bozzoni, et al.
Neuro-Degenerative Diseases|June 11, 2011
Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosisV Orsetti, E Pegoraro, V Cima, et al.
Neurology|June 8, 2011
ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansionG Sorarù, M Clementi, M Forzan, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Revue Neurologique|May 6, 2017
Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapyG Querin, G Sorarù, P-F Pradat
European Journal of Neurology|October 24, 2018
Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian regionC Bertolin, G Querin, I Martinelli, et al.
Revue Neurologique|November 15, 2024
Quantitative spinal cord imaging: Early ALS diagnosis and monitoring of disease progressionM Khamaysa, M El Mendili, V Marchand, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 29, 2017
The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA caseG Querin, I Martinelli, C Bertolin, et al.
Revue Neurologique|June 6, 2017
Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variantG Querin, P Corcia, T Lenglet, et al.
European Journal of Neurology|September 12, 2014
The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case reportG Querin, C Bertolin, A Martinuzzi, et al.
European Journal of Neurology|June 7, 2017
Spinal cord multi-parametric magnetic resonance imaging for survival prediction in amyotrophic lateral sclerosisG Querin, M M El Mendili, T Lenglet, et al.
European Journal of Neurology|February 22, 2018
New FIG4 gene mutations causing aggressive ALSC Bertolin, G Querin, V Bozzoni, et al.
Neuro-Degenerative Diseases|June 11, 2011
Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosisV Orsetti, E Pegoraro, V Cima, et al.
Neurology|June 8, 2011
ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansionG Sorarù, M Clementi, M Forzan, et al.
Pageof 3