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Showing results (131-140 of 166) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 9, 2013
Genetic counselling in ALS: facts, uncertainties and clinical suggestionsAdriano Chiò, Stefania Battistini, Andrea Calvo, et al.
Neurobiology of Aging|August 2, 2011
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTDGiuseppe Borghero, Gianluca Floris, Antonino Cannas, et al.
Neurology|December 21, 2014
ATXN2 polyQ intermediate repeats are a modifier of ALS survivalAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
Cell Death and Differentiation|May 16, 2021
Kupffer cell receptor CLEC4F is important for the destruction of desialylated platelets in miceYizhi Jiang, Yaqiong Tang, Christopher Hoover, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutationsAdriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Neuropathology and Applied Neurobiology|May 15, 2016
Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP-43 subcellular distributionG De Marco, A Lomartire, A Calvo, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patientsBryan J Traynor, Michael Nalls, Shiao-Lin Lai, et al.
Cytogenetic and Genome Research|December 15, 2015
Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/DuplicationsEleonora Di Gregorio, Giorgia Gai, Giovanni Botta, et al.
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
European Journal of Human Genetics : EJHG|April 25, 2013
Homozygosity analysis in amyotrophic lateral sclerosisKin Mok, Hannu Laaksovirta, Pentti J Tienari, et al.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Journal of Neurology, Neurosurgery, and Psychiatry|July 9, 2013
Genetic counselling in ALS: facts, uncertainties and clinical suggestionsAdriano Chiò, Stefania Battistini, Andrea Calvo, et al.
Neurobiology of Aging|August 2, 2011
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTDGiuseppe Borghero, Gianluca Floris, Antonino Cannas, et al.
Neurology|December 21, 2014
ATXN2 polyQ intermediate repeats are a modifier of ALS survivalAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
Cell Death and Differentiation|May 16, 2021
Kupffer cell receptor CLEC4F is important for the destruction of desialylated platelets in miceYizhi Jiang, Yaqiong Tang, Christopher Hoover, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutationsAdriano Chiò, Gabriella Restagno, Maura Brunetti, et al.
Neuropathology and Applied Neurobiology|May 15, 2016
Monocytes of patients with amyotrophic lateral sclerosis linked to gene mutations display altered TDP-43 subcellular distributionG De Marco, A Lomartire, A Calvo, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patientsBryan J Traynor, Michael Nalls, Shiao-Lin Lai, et al.
Cytogenetic and Genome Research|December 15, 2015
Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/DuplicationsEleonora Di Gregorio, Giorgia Gai, Giovanni Botta, et al.
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
European Journal of Human Genetics : EJHG|April 25, 2013
Homozygosity analysis in amyotrophic lateral sclerosisKin Mok, Hannu Laaksovirta, Pentti J Tienari, et al.
Pageof 17