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Alessandra Tessa

Showing results (1-10 of 116) with videos related to

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Neurogenetics|December 7, 2017
Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysisDaniele Galatolo, Alessandra Tessa, Alessandro Filla, et al.
Clinical Neurology and Neurosurgery|June 22, 2021
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 geneSara Locci, Silvia Bianchi, Alessandra Tessa, et al.
BMC Neurology|May 30, 2020
Docosahexaenoic acid in ARSACS: observations in two patientsIvana Ricca, Alessandra Tessa, Rosanna Trovato, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 23, 2013
Infantile-onset ascending hereditary spastic paralysis: a case report and brief literature reviewLoretta Racis, Alessandra Tessa, Maura Pugliatti, et al.
Stem Cell Research|June 18, 2024
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 geneMatteo Baggiani, Filippo Maria Santorelli, Serena Mero, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 10, 2019
SPG8 mutations in Italian families: clinical data and literature reviewFederica Ginanneschi, Angelica D'Amore, Melissa Barghigiani, et al.
Genetics Research International|May 9, 2012
Molecular investigation of pediatric portuguese patients with sensorineural hearing lossCélia Nogueira, Miguel Coutinho, Cristina Pereira, et al.
BMC Medical Genetics|April 3, 2014
Novel SPAST deletion and reduced DPY30 expression in a Spastic Paraplegia type 4 kindredLoretta Racis, Eugenia Storti, Maura Pugliatti, et al.
Journal of Cellular Physiology|July 20, 2017
Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localizationIlaria Taglia, Patrizia Formichi, Carla Battisti, et al.
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
Neurogenetics|December 7, 2017
Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysisDaniele Galatolo, Alessandra Tessa, Alessandro Filla, et al.
Clinical Neurology and Neurosurgery|June 22, 2021
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 geneSara Locci, Silvia Bianchi, Alessandra Tessa, et al.
BMC Neurology|May 30, 2020
Docosahexaenoic acid in ARSACS: observations in two patientsIvana Ricca, Alessandra Tessa, Rosanna Trovato, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 23, 2013
Infantile-onset ascending hereditary spastic paralysis: a case report and brief literature reviewLoretta Racis, Alessandra Tessa, Maura Pugliatti, et al.
Stem Cell Research|June 18, 2024
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 geneMatteo Baggiani, Filippo Maria Santorelli, Serena Mero, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 10, 2019
SPG8 mutations in Italian families: clinical data and literature reviewFederica Ginanneschi, Angelica D'Amore, Melissa Barghigiani, et al.
Genetics Research International|May 9, 2012
Molecular investigation of pediatric portuguese patients with sensorineural hearing lossCélia Nogueira, Miguel Coutinho, Cristina Pereira, et al.
BMC Medical Genetics|April 3, 2014
Novel SPAST deletion and reduced DPY30 expression in a Spastic Paraplegia type 4 kindredLoretta Racis, Eugenia Storti, Maura Pugliatti, et al.
Journal of Cellular Physiology|July 20, 2017
Primary familial brain calcification with a novel SLC20A2 mutation: Analysis of PiT-2 expression and localizationIlaria Taglia, Patrizia Formichi, Carla Battisti, et al.
Pageof 12