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Maria Valente

Showing results (131-140 of 358) with videos related to

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Stem Cell Research|April 24, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1Manuela Mura, Monia Ginevrino, Rita Zappatore, et al.
Stem Cell Research|December 1, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2013
Alpha-synuclein gene duplication: marked intrafamilial variability in two novel pedigreesAntonio E Elia, Simona Petrucci, Alfonso Fasano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 23, 2012
Successful subthalamic stimulation, but levodopa-induced dystonia, in a genetic Parkinson's diseaseAlessandro Stefani, Francesco Marzetti, Mariangela Pierantozzi, et al.
Annals of Neurology|September 7, 2004
PINK1 mutations are associated with sporadic early-onset parkinsonismEnza Maria Valente, Sergio Salvi, Tamara Ialongo, et al.
Journal of Cellular and Molecular Medicine|May 7, 2025
D- and L-Amino Acid Blood Concentrations Are Affected in Children With Duchenne Muscular DystrophyMartina Garofalo, Chiara Panicucci, Alberto Imarisio, et al.
Brain & Development|March 20, 2025
A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literatureDavide Politano, Francesca Marazzi, Ilaria Scognamillo, et al.
Parkinsonism & Related Disorders|March 31, 2024
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case reportAlberto Imarisio, Andrea Pilotto, Alessandro Lupini, et al.
Neurology. Genetics|May 18, 2026
<i>KIF5C</i>-Related Neurodevelopmental Disorder: Three New Cases and Additional Neuroradiologic InsightsDavide Politano, Simone Gana, Simona Orcesi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Pageof 36

Showing results (131-140 of 358) with videos related to

Sort By:
Pageof 36
Stem Cell Research|April 24, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1Manuela Mura, Monia Ginevrino, Rita Zappatore, et al.
Stem Cell Research|December 1, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1Manuela Mura, Francesca Bastaroli, Marzia Corli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2013
Alpha-synuclein gene duplication: marked intrafamilial variability in two novel pedigreesAntonio E Elia, Simona Petrucci, Alfonso Fasano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 23, 2012
Successful subthalamic stimulation, but levodopa-induced dystonia, in a genetic Parkinson's diseaseAlessandro Stefani, Francesco Marzetti, Mariangela Pierantozzi, et al.
Annals of Neurology|September 7, 2004
PINK1 mutations are associated with sporadic early-onset parkinsonismEnza Maria Valente, Sergio Salvi, Tamara Ialongo, et al.
Journal of Cellular and Molecular Medicine|May 7, 2025
D- and L-Amino Acid Blood Concentrations Are Affected in Children With Duchenne Muscular DystrophyMartina Garofalo, Chiara Panicucci, Alberto Imarisio, et al.
Brain & Development|March 20, 2025
A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literatureDavide Politano, Francesca Marazzi, Ilaria Scognamillo, et al.
Parkinsonism & Related Disorders|March 31, 2024
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case reportAlberto Imarisio, Andrea Pilotto, Alessandro Lupini, et al.
Neurology. Genetics|May 18, 2026
<i>KIF5C</i>-Related Neurodevelopmental Disorder: Three New Cases and Additional Neuroradiologic InsightsDavide Politano, Simone Gana, Simona Orcesi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Pageof 36