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Maria Valente

Showing results (161-170 of 358) with videos related to

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Stem Cell Research|April 23, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Stem Cell Research|April 12, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Journal of Neurology|June 28, 2008
Subclinical sensory abnormalities in unaffected PINK1 heterozygotesMirta Fiorio, Enza Maria Valente, Mattia Gambarin, et al.
American Journal of Medical Genetics. Part A|July 4, 2025
Pulmonary Arterial Hypertension Onset in an Adult Woman With a TBX4 Likely Pathogenic Variant Following Imatinib Administration: A Case ReportSimone Carbonera, Laura Scelsi, Alessandra Greco, et al.
Neurology. Genetics|November 8, 2024
Bilateral Dentate Nuclei Hyperintensities and Response to 4-Aminopyridine in a Patient With Childhood-Onset GAA-<i>FGF14</i>-Related AtaxiaPierfrancesco Mitrotti, Elisa Vegezzi, Roberta Zangaglia, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|May 19, 2009
[Serological evaluation for detection of anti-Leishmania antibodies in dogs and cats in the district of Santa Rita de Cássia, municipality of Barra Mansa, State of Rio de Janeiro]Fabiano Borges Figueiredo, Isabel Cristina Fábregas Bonna, Lílian Dias Nascimento, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Brain : a Journal of Neurology|November 16, 2006
Defective temporal processing of sensory stimuli in DYT1 mutation carriers: a new endophenotype of dystonia?Mirta Fiorio, Mattia Gambarin, Enza Maria Valente, et al.
Brain Imaging and Behavior|April 3, 2015
A rare case of cerebellar agenesis: a probabilistic Constrained Spherical Deconvolution tractographic studyEnricomaria Mormina, Marilena Briguglio, Rosa Morabito, et al.
Clinical Interventions in Aging|November 4, 2015
Body composition as a frailty marker for the elderly communityGláucia Regina Falsarella, Lívia Pimenta Renó Gasparotto, Caroline Coutinho Barcelos, et al.
Pageof 36

Showing results (161-170 of 358) with videos related to

Sort By:
Pageof 36
Stem Cell Research|April 23, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Stem Cell Research|April 12, 2019
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutationManuela Mura, Yee-Ki Lee, Federica Pisano, et al.
Journal of Neurology|June 28, 2008
Subclinical sensory abnormalities in unaffected PINK1 heterozygotesMirta Fiorio, Enza Maria Valente, Mattia Gambarin, et al.
American Journal of Medical Genetics. Part A|July 4, 2025
Pulmonary Arterial Hypertension Onset in an Adult Woman With a TBX4 Likely Pathogenic Variant Following Imatinib Administration: A Case ReportSimone Carbonera, Laura Scelsi, Alessandra Greco, et al.
Neurology. Genetics|November 8, 2024
Bilateral Dentate Nuclei Hyperintensities and Response to 4-Aminopyridine in a Patient With Childhood-Onset GAA-<i>FGF14</i>-Related AtaxiaPierfrancesco Mitrotti, Elisa Vegezzi, Roberta Zangaglia, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|May 19, 2009
[Serological evaluation for detection of anti-Leishmania antibodies in dogs and cats in the district of Santa Rita de Cássia, municipality of Barra Mansa, State of Rio de Janeiro]Fabiano Borges Figueiredo, Isabel Cristina Fábregas Bonna, Lílian Dias Nascimento, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Brain : a Journal of Neurology|November 16, 2006
Defective temporal processing of sensory stimuli in DYT1 mutation carriers: a new endophenotype of dystonia?Mirta Fiorio, Mattia Gambarin, Enza Maria Valente, et al.
Brain Imaging and Behavior|April 3, 2015
A rare case of cerebellar agenesis: a probabilistic Constrained Spherical Deconvolution tractographic studyEnricomaria Mormina, Marilena Briguglio, Rosa Morabito, et al.
Clinical Interventions in Aging|November 4, 2015
Body composition as a frailty marker for the elderly communityGláucia Regina Falsarella, Lívia Pimenta Renó Gasparotto, Caroline Coutinho Barcelos, et al.
Pageof 36