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Revue Neurologique
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May 6, 2017
Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy
G 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 region
C Bertolin, G Querin, I Martinelli, et al.
Revue Neurologique
|
November 15, 2024
Quantitative spinal cord imaging: Early ALS diagnosis and monitoring of disease progression
M 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 case
G 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 variant
G 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 report
G 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 sclerosis
G Querin, M M El Mendili, T Lenglet, et al.
European Journal of Neurology
|
February 22, 2018
New FIG4 gene mutations causing aggressive ALS
C 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 sclerosis
V Orsetti, E Pegoraro, V Cima, et al.
Neurology
|
June 8, 2011
ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion
G Sorarù, M Clementi, M Forzan, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Revue Neurologique
|
May 6, 2017
Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy
G 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 region
C Bertolin, G Querin, I Martinelli, et al.
Revue Neurologique
|
November 15, 2024
Quantitative spinal cord imaging: Early ALS diagnosis and monitoring of disease progression
M 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 case
G 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 variant
G 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 report
G 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 sclerosis
G Querin, M M El Mendili, T Lenglet, et al.
European Journal of Neurology
|
February 22, 2018
New FIG4 gene mutations causing aggressive ALS
C 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 sclerosis
V Orsetti, E Pegoraro, V Cima, et al.
Neurology
|
June 8, 2011
ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion
G Sorarù, M Clementi, M Forzan, et al.
Page
of 3