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International Journal of Molecular Sciences
|
August 27, 2021
Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Valentina Naef, Maria Marchese, Asahi Ogi, et al.
Annals of Clinical and Translational Neurology
|
June 5, 2024
SCAR32: Functional characterization and expansion of the clinical-genetic spectrum
Valentina Naef, Maria Lieto, Sara Satolli, et al.
ACS Applied Optical Materials
|
May 4, 2026
Polydopamine Nanoparticles as Label-Free Contrast Agents in Photoacoustic Imaging <i>In Vitro</i> and <i>In Vivo</i>
Matteo Battaglini, Paolo Armanetti, Alessio Carmignani, et al.
Cell Death & Disease
|
February 20, 2026
Loss of function variants in HPDL impair human cortical development via alterations of mitochondrial function
Matteo Baggiani, Maria Andrea Desbats, Valentina Naef, et al.
Journal of Neurology
|
March 11, 2021
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ<sub>10</sub> deficiency in muscle or skin fibroblasts
Serena Mero, Leonardo Salviati, Vincenzo Leuzzi, et al.
Annals of Clinical and Translational Neurology
|
March 28, 2020
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52
Angelica D'Amore, Alessandra Tessa, Valentina Naef, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 28, 2025
HPDL Biallelic Variants in Cerebral Palsy and Childhood-Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights
Serena Mero, Sara Satolli, Daniele Galatolo, et al.
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Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
International Journal of Molecular Sciences
|
August 27, 2021
Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
Valentina Naef, Maria Marchese, Asahi Ogi, et al.
Annals of Clinical and Translational Neurology
|
June 5, 2024
SCAR32: Functional characterization and expansion of the clinical-genetic spectrum
Valentina Naef, Maria Lieto, Sara Satolli, et al.
ACS Applied Optical Materials
|
May 4, 2026
Polydopamine Nanoparticles as Label-Free Contrast Agents in Photoacoustic Imaging <i>In Vitro</i> and <i>In Vivo</i>
Matteo Battaglini, Paolo Armanetti, Alessio Carmignani, et al.
Cell Death & Disease
|
February 20, 2026
Loss of function variants in HPDL impair human cortical development via alterations of mitochondrial function
Matteo Baggiani, Maria Andrea Desbats, Valentina Naef, et al.
Journal of Neurology
|
March 11, 2021
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ<sub>10</sub> deficiency in muscle or skin fibroblasts
Serena Mero, Leonardo Salviati, Vincenzo Leuzzi, et al.
Annals of Clinical and Translational Neurology
|
March 28, 2020
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52
Angelica D'Amore, Alessandra Tessa, Valentina Naef, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 28, 2025
HPDL Biallelic Variants in Cerebral Palsy and Childhood-Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights
Serena Mero, Sara Satolli, Daniele Galatolo, et al.
Page
of 3