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Lorena Travaglini

Showing results (11-20 of 74) with videos related to

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International Journal of Molecular Sciences|May 24, 2020
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic AtaxiasGiacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
International Journal of Molecular Sciences|April 12, 2013
Frataxin deficiency leads to reduced expression and impaired translocation of NF-E2-related factor (Nrf2) in cultured motor neuronsValentina D'Oria, Stefania Petrini, Lorena Travaglini, et al.
BMC Medical Genetics|July 25, 2015
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: a detailed phenotype descriptionRoberta Battini, Silvano Bertelloni, Guja Astrea, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center studyVito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Cerebellum (London, England)|February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 MutationsTommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
European Journal of Pediatrics|November 5, 2014
Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancyIsabella Giovannoni, Francesco Callea, Lorena Travaglini, et al.
Frontiers in Neurology|April 4, 2024
Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander diseaseCarmela Romano, Emanuele Morena, Simona Petrucci, et al.
International Journal of Molecular Sciences|April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasisBarbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, et al.
Pageof 8

Showing results (11-20 of 74) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Sciences|May 24, 2020
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic AtaxiasGiacomo Garone, Alessandro Capuano, Lorena Travaglini, et al.
International Journal of Molecular Sciences|April 12, 2013
Frataxin deficiency leads to reduced expression and impaired translocation of NF-E2-related factor (Nrf2) in cultured motor neuronsValentina D'Oria, Stefania Petrini, Lorena Travaglini, et al.
BMC Medical Genetics|July 25, 2015
Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: a detailed phenotype descriptionRoberta Battini, Silvano Bertelloni, Guja Astrea, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 17, 2025
Genotype variability in early-onset Hereditary Spastic Paraplegia: a single-center studyVito Luigi Colona, Lorena Travaglini, Jacopo Sartorelli, et al.
Cerebellum (London, England)|February 5, 2018
Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 MutationsTommaso Schirinzi, Federica Graziola, Francesco Nicita, et al.
European Journal of Pediatrics|November 5, 2014
Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancyIsabella Giovannoni, Francesco Callea, Lorena Travaglini, et al.
Frontiers in Neurology|April 4, 2024
Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander diseaseCarmela Romano, Emanuele Morena, Simona Petrucci, et al.
International Journal of Molecular Sciences|April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasisBarbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Brain & Development|February 4, 2018
ATP1A3-related epileptic encephalopathy responding to ketogenic dietTommaso Schirinzi, Federica Graziola, Raffaella Cusmai, et al.
Pageof 8