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Roberta Zuntini

Showing results (11-20 of 47) with videos related to

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Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 17, 2016
Molecular detection and genetic characterization of circulating measles virus in northern ItalyGiulia Piccirilli, Angela Chiereghin, Maria Grazia Pascucci, et al.
Biotechnology Advances|June 22, 2011
Searching for a needle in the haystack: comparing six methods to evaluate heteroplasmy in difficult sequence contextIvana Kurelac, Martin Lang, Roberta Zuntini, et al.
Brain & Development|June 4, 2023
Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant in the CLCN4 gene: A case reportJessica Rossi, Marco Russo, Giuseppe Gobbi, et al.
The Journal of Experimental Medicine|August 22, 2007
Mutations of the Igbeta gene cause agammaglobulinemia in manSimona Ferrari, Vassilios Lougaris, Stefano Caraffi, et al.
Developmental Medicine and Child Neurology|May 20, 2011
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotypeCaterina Garone, Tommaso Pippucci, Duccio M Cordelli, et al.
Journal of the Neurological Sciences|October 10, 2017
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophyGrazia Iannello, Claudio Graziano, Giovanna Cenacchi, et al.
Journal of the Neurological Sciences|December 20, 2017
Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212]Grazia Iannello, Claudio Graziano, Giovanna Cenacchi, et al.
Fetal and Pediatric Pathology|September 25, 2023
Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the <i>SOX2</i> Gene: Ultrasound, Pathological, and Cytogenetic FindingsMaria Paola Bonasoni, Giuseppina Comitini, Mariangela Pati, et al.
BMC Cancer|February 7, 2014
A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancerLaura Maria Pradella, Cecilia Evangelisti, Claudia Ligorio, et al.
Diagnostics (Basel, Switzerland)|August 28, 2025
A Partial Hydatidiform Mole in an Ovarian Ectopic Pregnancy: An Exceptional OccurrenceMaria Paola Bonasoni, Roberta Zuntini, Khush Shah, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 17, 2016
Molecular detection and genetic characterization of circulating measles virus in northern ItalyGiulia Piccirilli, Angela Chiereghin, Maria Grazia Pascucci, et al.
Biotechnology Advances|June 22, 2011
Searching for a needle in the haystack: comparing six methods to evaluate heteroplasmy in difficult sequence contextIvana Kurelac, Martin Lang, Roberta Zuntini, et al.
Brain & Development|June 4, 2023
Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant in the CLCN4 gene: A case reportJessica Rossi, Marco Russo, Giuseppe Gobbi, et al.
The Journal of Experimental Medicine|August 22, 2007
Mutations of the Igbeta gene cause agammaglobulinemia in manSimona Ferrari, Vassilios Lougaris, Stefano Caraffi, et al.
Developmental Medicine and Child Neurology|May 20, 2011
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotypeCaterina Garone, Tommaso Pippucci, Duccio M Cordelli, et al.
Journal of the Neurological Sciences|October 10, 2017
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophyGrazia Iannello, Claudio Graziano, Giovanna Cenacchi, et al.
Journal of the Neurological Sciences|December 20, 2017
Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212]Grazia Iannello, Claudio Graziano, Giovanna Cenacchi, et al.
Fetal and Pediatric Pathology|September 25, 2023
Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the <i>SOX2</i> Gene: Ultrasound, Pathological, and Cytogenetic FindingsMaria Paola Bonasoni, Giuseppina Comitini, Mariangela Pati, et al.
BMC Cancer|February 7, 2014
A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancerLaura Maria Pradella, Cecilia Evangelisti, Claudia Ligorio, et al.
Diagnostics (Basel, Switzerland)|August 28, 2025
A Partial Hydatidiform Mole in an Ovarian Ectopic Pregnancy: An Exceptional OccurrenceMaria Paola Bonasoni, Roberta Zuntini, Khush Shah, et al.
Pageof 5