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Guido Primiano

Showing results (61-70 of 84) with videos related to

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Journal of Neurology|April 15, 2025
Elevated serum concentrations of GFAP in hereditary transthyretin amyloidosis since pre-symptomatic stagesDomenico Plantone, Marco Luigetti, Carlo Manco, et al.
Journal of Neurology|July 15, 2019
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variantsFrancesco Nicita, Fabrizia Stregapede, Alessandra Tessa, et al.
Journal of the Peripheral Nervous System : JPNS|August 3, 2023
Quantitative sensory testing and skin biopsy findings in late-onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)Luca Leonardi, Rocco Costanzo, Francesca Forcina, et al.
Journal of Neurology|February 3, 2019
Muscle pain in mitochondrial diseases: a picture from the Italian networkMassimiliano Filosto, Stefano Cotti Piccinelli, Costanza Lamperti, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 16, 2026
Serum peripherin as a disease biomarker in hereditary transthyretin amyloidosis: a multicenter cohort studyDomenico Plantone, Delia Righi, Angela Romano, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
European Journal of Neurology|June 4, 2025
Comparative Analysis of SiMoA and Ella Immunoassay Platforms for Measuring Serum Neurofilament Light Chain Levels in ATTRv With Polyneuropathy and Presymptomatic CarriersGuido Primiano, Marco Luigetti, Delia Righi, et al.
Neurogenetics|January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian surveyChiara Ticci, Federico Sicca, Anna Ardissone, et al.
Neurology|March 20, 2025
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8Sara Carli, Anna Levarlet, Daria Diodato, et al.
European Journal of Neurology|October 28, 2022
Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID-19 RegistryChiara Pizzamiglio, Robert D S Pitceathly, Michael P Lunn, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Journal of Neurology|April 15, 2025
Elevated serum concentrations of GFAP in hereditary transthyretin amyloidosis since pre-symptomatic stagesDomenico Plantone, Marco Luigetti, Carlo Manco, et al.
Journal of Neurology|July 15, 2019
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variantsFrancesco Nicita, Fabrizia Stregapede, Alessandra Tessa, et al.
Journal of the Peripheral Nervous System : JPNS|August 3, 2023
Quantitative sensory testing and skin biopsy findings in late-onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)Luca Leonardi, Rocco Costanzo, Francesca Forcina, et al.
Journal of Neurology|February 3, 2019
Muscle pain in mitochondrial diseases: a picture from the Italian networkMassimiliano Filosto, Stefano Cotti Piccinelli, Costanza Lamperti, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 16, 2026
Serum peripherin as a disease biomarker in hereditary transthyretin amyloidosis: a multicenter cohort studyDomenico Plantone, Delia Righi, Angela Romano, et al.
Neurology. Genetics|November 19, 2020
Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from ItalyVincenzo Montano, Francesco Gruosso, Valerio Carelli, et al.
European Journal of Neurology|June 4, 2025
Comparative Analysis of SiMoA and Ella Immunoassay Platforms for Measuring Serum Neurofilament Light Chain Levels in ATTRv With Polyneuropathy and Presymptomatic CarriersGuido Primiano, Marco Luigetti, Delia Righi, et al.
Neurogenetics|January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian surveyChiara Ticci, Federico Sicca, Anna Ardissone, et al.
Neurology|March 20, 2025
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8Sara Carli, Anna Levarlet, Daria Diodato, et al.
European Journal of Neurology|October 28, 2022
Factors associated with the severity of COVID-19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID-19 RegistryChiara Pizzamiglio, Robert D S Pitceathly, Michael P Lunn, et al.
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