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Journal of Medical Genetics
|
June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations
Stéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
July 9, 2008
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis
Wendy J Broom, Matthew Greenway, Ghazaleh Sadri-Vakili, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 2021
Effect of familial clustering in the genetic screening of 235 French ALS families
Philippe Corcia, William Camu, Celine Brulard, et al.
Plos One
|
May 21, 2014
Safety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trial
Vincent Meininger, Pierre-François Pradat, Andrea Corse, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunities
François Muratet, Elisa Teyssou, Aude Chiot, et al.
Biomedicines
|
March 29, 2023
The <i>HFE</i> p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with <i>SOD1</i> Mutations
Antonio Canosa, Andrea Calvo, Gabriele Mora, et al.
Plos One
|
April 18, 2012
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS
Frank P Diekstra, Christiaan G J Saris, Wouter van Rheenen, et al.
Journal of Alzheimer'S Disease : JAD
|
December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing
Isabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.
Human Molecular Genetics
|
November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
An Goris, Jessica van Setten, Frank Diekstra, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
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of 15
Search research articles
Search
Showing results (121-130 of 142) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations
Stéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
July 9, 2008
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis
Wendy J Broom, Matthew Greenway, Ghazaleh Sadri-Vakili, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 2021
Effect of familial clustering in the genetic screening of 235 French ALS families
Philippe Corcia, William Camu, Celine Brulard, et al.
Plos One
|
May 21, 2014
Safety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trial
Vincent Meininger, Pierre-François Pradat, Andrea Corse, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunities
François Muratet, Elisa Teyssou, Aude Chiot, et al.
Biomedicines
|
March 29, 2023
The <i>HFE</i> p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with <i>SOD1</i> Mutations
Antonio Canosa, Andrea Calvo, Gabriele Mora, et al.
Plos One
|
April 18, 2012
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS
Frank P Diekstra, Christiaan G J Saris, Wouter van Rheenen, et al.
Journal of Alzheimer'S Disease : JAD
|
December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing
Isabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.
Human Molecular Genetics
|
November 16, 2013
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
An Goris, Jessica van Setten, Frank Diekstra, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
Page
of 15