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Carla Lintas

Showing results (41-50 of 52) with videos related to

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Frontiers in Neuroscience|January 22, 2024
A pathogenic variant in the <i>FLCN</i> gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?Irene Bottillo, Luigi Laino, Alessia Azzarà, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorderFrancesca Cucinotta, Carla Lintas, Pasquale Tomaiuolo, et al.
Acta Neuropsychiatrica|April 30, 2021
Molecular biomarkers to track clinical improvement following an integrative treatment model in autistic toddlersIgnazio S Piras, Filippo Manti, Anna Costa, et al.
International Journal of Molecular Sciences|February 11, 2023
Phytochemicals as Immunomodulatory Agents in MelanomaClaudio Tabolacci, Daniela De Vita, Antonio Facchiano, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 12, 2020
Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association studyIgnazio Stefano Piras, Chiara Picinelli, Raffaele Iennaco, et al.
Journal of Medical Virology|November 12, 2021
SARS-CoV-2 AY.4.2 variant circulating in Italy: Genomic preliminary insightSilvia Angeletti, Marta Giovanetti, Marta Fogolari, et al.
Psychiatry Research|May 22, 2010
Decreased serum arylesterase activity in autism spectrum disordersLaura Gaita, Barbara Manzi, Roberto Sacco, et al.
Journal of Neurodevelopmental Disorders|May 27, 2026
Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndromeLaura Sandoni, Fethia Chehbani, Lisa Asta, et al.
BMC Medicine|October 23, 2009
Genomic and epigenetic evidence for oxytocin receptor deficiency in autismSimon G Gregory, Jessica J Connelly, Aaron J Towers, et al.
Molecular Genetics & Genomic Medicine|June 27, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex familyFrancesca Cucinotta, Arianna Ricciardello, Laura Turriziani, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Neuroscience|January 22, 2024
A pathogenic variant in the <i>FLCN</i> gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?Irene Bottillo, Luigi Laino, Alessia Azzarà, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorderFrancesca Cucinotta, Carla Lintas, Pasquale Tomaiuolo, et al.
Acta Neuropsychiatrica|April 30, 2021
Molecular biomarkers to track clinical improvement following an integrative treatment model in autistic toddlersIgnazio S Piras, Filippo Manti, Anna Costa, et al.
International Journal of Molecular Sciences|February 11, 2023
Phytochemicals as Immunomodulatory Agents in MelanomaClaudio Tabolacci, Daniela De Vita, Antonio Facchiano, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 12, 2020
Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association studyIgnazio Stefano Piras, Chiara Picinelli, Raffaele Iennaco, et al.
Journal of Medical Virology|November 12, 2021
SARS-CoV-2 AY.4.2 variant circulating in Italy: Genomic preliminary insightSilvia Angeletti, Marta Giovanetti, Marta Fogolari, et al.
Psychiatry Research|May 22, 2010
Decreased serum arylesterase activity in autism spectrum disordersLaura Gaita, Barbara Manzi, Roberto Sacco, et al.
Journal of Neurodevelopmental Disorders|May 27, 2026
Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndromeLaura Sandoni, Fethia Chehbani, Lisa Asta, et al.
BMC Medicine|October 23, 2009
Genomic and epigenetic evidence for oxytocin receptor deficiency in autismSimon G Gregory, Jessica J Connelly, Aaron J Towers, et al.
Molecular Genetics & Genomic Medicine|June 27, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex familyFrancesca Cucinotta, Arianna Ricciardello, Laura Turriziani, et al.
Pageof 6