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Maria Valente

Showing results (141-150 of 358) with videos related to

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Stem Cell Research|October 3, 2020
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 geneEltahir Ali, Rosalba Monica Ferraro, Gaetana Lanzi, et al.
Archives of Gerontology and Geriatrics|August 30, 2011
Impact of rheumatic diseases and chronic joint symptoms on quality of life in the elderlyGláucia Regina Falsarella, Ibsen Bellini Coimbra, Anita Liberalesso Neri, et al.
Computer Methods and Programs in Biomedicine|December 18, 2019
Development of SaraHome: A novel, well-accepted, technology-based assessment tool for patients with ataxiaSusanna Summa, Tommaso Schirinzi, Giuseppe Massimo Bernava, et al.
The Science of the Total Environment|December 21, 2025
Mine waste as a dual threat and opportunity: Linking mineralogy to environmental impact and critical element recoveryAna Barroso, Isabel Margarida Horta Ribeiro Antunes, Maria Amália Sequeira Braga, et al.
Archives of Endocrinology and Metabolism|December 5, 2022
A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?Roberto Franceschi, Evelina Maines, Maria Bellizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2006
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonismChiara Criscuolo, Giampiero Volpe, Anna De Rosa, et al.
Stem Cell Research|August 10, 2019
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder populationManuela Mura, Federica Pisano, Manuela Stefanello, et al.
Cerebellum (London, England)|February 9, 2024
Cerebellar Heterotopia: Broadening the Neuroradiological Spectrum of KBG SyndromeAdelaide Carrara, Camilla Mangiarotti, Ludovica Pasca, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 29, 2006
Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystoniaMattia Gambarin, Enza Maria Valente, Paolo Liberini, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 12, 2011
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenitaAnna Modoni, Adele D'Amico, Bruno Dallapiccola, et al.
Pageof 36

Showing results (141-150 of 358) with videos related to

Sort By:
Pageof 36
Stem Cell Research|October 3, 2020
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 geneEltahir Ali, Rosalba Monica Ferraro, Gaetana Lanzi, et al.
Archives of Gerontology and Geriatrics|August 30, 2011
Impact of rheumatic diseases and chronic joint symptoms on quality of life in the elderlyGláucia Regina Falsarella, Ibsen Bellini Coimbra, Anita Liberalesso Neri, et al.
Computer Methods and Programs in Biomedicine|December 18, 2019
Development of SaraHome: A novel, well-accepted, technology-based assessment tool for patients with ataxiaSusanna Summa, Tommaso Schirinzi, Giuseppe Massimo Bernava, et al.
The Science of the Total Environment|December 21, 2025
Mine waste as a dual threat and opportunity: Linking mineralogy to environmental impact and critical element recoveryAna Barroso, Isabel Margarida Horta Ribeiro Antunes, Maria Amália Sequeira Braga, et al.
Archives of Endocrinology and Metabolism|December 5, 2022
A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?Roberto Franceschi, Evelina Maines, Maria Bellizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2006
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonismChiara Criscuolo, Giampiero Volpe, Anna De Rosa, et al.
Stem Cell Research|August 10, 2019
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder populationManuela Mura, Federica Pisano, Manuela Stefanello, et al.
Cerebellum (London, England)|February 9, 2024
Cerebellar Heterotopia: Broadening the Neuroradiological Spectrum of KBG SyndromeAdelaide Carrara, Camilla Mangiarotti, Ludovica Pasca, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 29, 2006
Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystoniaMattia Gambarin, Enza Maria Valente, Paolo Liberini, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 12, 2011
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenitaAnna Modoni, Adele D'Amico, Bruno Dallapiccola, et al.
Pageof 36