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Ferdinando Squitieri

Showing results (121-130 of 147) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 23, 2017
Phosphorylation of huntingtin at residue T3 is decreased in Huntington's disease and modulates mutant huntingtin protein conformationCristina Cariulo, Lucia Azzollini, Margherita Verani, et al.
European Journal of Neurology|November 24, 2022
Economic burden of Huntington disease in Europe and the USA: Results from the Huntington's Disease Burden of Illness studyIdaira Rodríguez-Santana, Tiago Mestre, Ferdinando Squitieri, et al.
Annals of Neurology|December 15, 2018
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington diseaseImma Castaldo, Mariarosaria De Rosa, Antonella Romano, et al.
Frontiers in Neurology|September 30, 2021
Study Protocol for the Development of a European eHealth Platform to Improve Quality of Life in Individuals With Huntington's Disease and Their Partners (HD-eHelp Study): A User-Centered Design ApproachPearl J C van Lonkhuizen, Niko J H Vegt, Eline Meijer, et al.
Frontiers in Neurology|July 24, 2019
International Guidelines for the Treatment of Huntington's DiseaseAnne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 25, 2011
What is the impact of education on Huntington's disease?Jose Luis López-Sendón, Ana Royuela, Patricia Trigo, et al.
American Journal of Human Genetics|November 12, 2019
A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington DiseaseChris Kay, Jennifer A Collins, Nicholas S Caron, et al.
American Journal of Human Genetics|November 19, 2003
Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformationsChristina L Liquori, Michel J Berg, Adrian M Siegel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 21, 2018
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general populationChris Kay, Jennifer A Collins, Galen E B Wright, et al.
The Lancet. Neurology|September 24, 2018
Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysisCaterina Fusilli, Simone Migliore, Tommaso Mazza, et al.
Pageof 15

Showing results (121-130 of 147) with videos related to

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Pageof 15
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2017
Phosphorylation of huntingtin at residue T3 is decreased in Huntington's disease and modulates mutant huntingtin protein conformationCristina Cariulo, Lucia Azzollini, Margherita Verani, et al.
European Journal of Neurology|November 24, 2022
Economic burden of Huntington disease in Europe and the USA: Results from the Huntington's Disease Burden of Illness studyIdaira Rodríguez-Santana, Tiago Mestre, Ferdinando Squitieri, et al.
Annals of Neurology|December 15, 2018
DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington diseaseImma Castaldo, Mariarosaria De Rosa, Antonella Romano, et al.
Frontiers in Neurology|September 30, 2021
Study Protocol for the Development of a European eHealth Platform to Improve Quality of Life in Individuals With Huntington's Disease and Their Partners (HD-eHelp Study): A User-Centered Design ApproachPearl J C van Lonkhuizen, Niko J H Vegt, Eline Meijer, et al.
Frontiers in Neurology|July 24, 2019
International Guidelines for the Treatment of Huntington's DiseaseAnne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 25, 2011
What is the impact of education on Huntington's disease?Jose Luis López-Sendón, Ana Royuela, Patricia Trigo, et al.
American Journal of Human Genetics|November 12, 2019
A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington DiseaseChris Kay, Jennifer A Collins, Nicholas S Caron, et al.
American Journal of Human Genetics|November 19, 2003
Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformationsChristina L Liquori, Michel J Berg, Adrian M Siegel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 21, 2018
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general populationChris Kay, Jennifer A Collins, Galen E B Wright, et al.
The Lancet. Neurology|September 24, 2018
Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysisCaterina Fusilli, Simone Migliore, Tommaso Mazza, et al.
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