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Filomena My

Showing results (1-10 of 12) with videos related to

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Functional Neurology|May 23, 2003
Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosisFrancesco Fattapposta, Filomena My, Donatella Valente, et al.
Clinical Neurology and Neurosurgery|May 22, 2021
Recurrent Miller-Fisher syndrome overlapping Guillain-Barrè syndrome and Bickerstaff brainstem encephalitis: A case reportGaetano Barbagallo, Marcella Caggiula, Angela Lupo, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|September 21, 2018
[A case of Anderson-Fabry disease: a multidisciplinary approach for diagnosis and follow up]Anna Zito, Antonio De Pascalis, Annarita Armeni, et al.
BMC Genomics|March 25, 2017
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosisAndrea Iorio, Flavio De Angelis, Marco Di Girolamo, et al.
JACC. Cardiovascular Imaging|December 23, 2019
Low Sensitivity of Bone Scintigraphy in Detecting Phe64Leu Mutation-Related Transthyretin Cardiac AmyloidosisMaria Beatrice Musumeci, Francesco Cappelli, Domitilla Russo, et al.
Brain Sciences|July 29, 2025
Prediction of Parkinson Disease Using Long-Term, Short-Term Acoustic Features Based on Machine LearningMehdi Rashidi, Serena Arima, Andrea Claudio Stetco, et al.
European Journal of Human Genetics : EJHG|June 22, 2017
Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosisAndrea Iorio, Antonella De Lillo, Flavio De Angelis, et al.
European Journal of Neurology|March 15, 2022
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in ItalyMarco Luigetti, Giovanni Antonini, Andrea Di Paolantonio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 1, 2024
Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in ItalyLuca Gentile, Anna Mazzeo, Chiara Briani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 15, 2024
Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in ItalyLuca Gentile, Anna Mazzeo, Chiara Briani, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Functional Neurology|May 23, 2003
Preprogramming motor dysfunction in paroxysmal kinesigenic choreoathetosisFrancesco Fattapposta, Filomena My, Donatella Valente, et al.
Clinical Neurology and Neurosurgery|May 22, 2021
Recurrent Miller-Fisher syndrome overlapping Guillain-Barrè syndrome and Bickerstaff brainstem encephalitis: A case reportGaetano Barbagallo, Marcella Caggiula, Angela Lupo, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|September 21, 2018
[A case of Anderson-Fabry disease: a multidisciplinary approach for diagnosis and follow up]Anna Zito, Antonio De Pascalis, Annarita Armeni, et al.
BMC Genomics|March 25, 2017
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosisAndrea Iorio, Flavio De Angelis, Marco Di Girolamo, et al.
JACC. Cardiovascular Imaging|December 23, 2019
Low Sensitivity of Bone Scintigraphy in Detecting Phe64Leu Mutation-Related Transthyretin Cardiac AmyloidosisMaria Beatrice Musumeci, Francesco Cappelli, Domitilla Russo, et al.
Brain Sciences|July 29, 2025
Prediction of Parkinson Disease Using Long-Term, Short-Term Acoustic Features Based on Machine LearningMehdi Rashidi, Serena Arima, Andrea Claudio Stetco, et al.
European Journal of Human Genetics : EJHG|June 22, 2017
Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosisAndrea Iorio, Antonella De Lillo, Flavio De Angelis, et al.
European Journal of Neurology|March 15, 2022
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in ItalyMarco Luigetti, Giovanni Antonini, Andrea Di Paolantonio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 1, 2024
Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in ItalyLuca Gentile, Anna Mazzeo, Chiara Briani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 15, 2024
Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in ItalyLuca Gentile, Anna Mazzeo, Chiara Briani, et al.
Pageof 2