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Donatella Greco

Showing results (21-30 of 41) with videos related to

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Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
International Journal of Molecular Sciences|April 14, 2026
Unraveling the Genetic and Molecular Architecture of Autism Spectrum Disorder: Implications for Clinical Genetics and Genomic DiagnosticsSimone Treccarichi, Mirella Vinci, Miriam Virgillito, et al.
Clinical Genetics|January 7, 2026
White-Sutton Syndrome: Insight of an Italian Cohort of 19 SubjectsAnna Facchini, Maria Pina Concas, Stefania Zampieri, et al.
International Journal of Molecular Sciences|February 13, 2026
Potential Link Between a Disruptive <i>CAPN6</i> Variant and Neurodevelopmental DisordersFrancesco Calì, Simone Treccarichi, Mirella Vinci, et al.
Neuromolecular Medicine|February 19, 2026
Searching for New Possible Peripheral Biomarkers of Cognitive Decline in Down Syndrome: The Role of IL-18 Pathway and its Interaction with TGF-β1 and TNF-αMargherita Grasso, Annamaria Fidilio, Francesca L'Episcopo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocationMaria Antonietta Di Bella, Francesco Calì, Gregorio Seidita, et al.
BMJ Open|August 9, 2020
Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents' experiences through a multicentre narrative medicine researchLetizia Ragusa, Antonio Crinò, Graziano Grugni, et al.
Frontiers in Pharmacology|April 5, 2024
Low TGF-β1 plasma levels are associated with cognitive decline in Down syndromeMargherita Grasso, Annamaria Fidilio, Francesca L'Episcopo, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteriaGiuseppe Marangi, Stefania Ricciardi, Daniela Orteschi, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndromeVittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

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Pageof 5
Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
International Journal of Molecular Sciences|April 14, 2026
Unraveling the Genetic and Molecular Architecture of Autism Spectrum Disorder: Implications for Clinical Genetics and Genomic DiagnosticsSimone Treccarichi, Mirella Vinci, Miriam Virgillito, et al.
Clinical Genetics|January 7, 2026
White-Sutton Syndrome: Insight of an Italian Cohort of 19 SubjectsAnna Facchini, Maria Pina Concas, Stefania Zampieri, et al.
International Journal of Molecular Sciences|February 13, 2026
Potential Link Between a Disruptive <i>CAPN6</i> Variant and Neurodevelopmental DisordersFrancesco Calì, Simone Treccarichi, Mirella Vinci, et al.
Neuromolecular Medicine|February 19, 2026
Searching for New Possible Peripheral Biomarkers of Cognitive Decline in Down Syndrome: The Role of IL-18 Pathway and its Interaction with TGF-β1 and TNF-αMargherita Grasso, Annamaria Fidilio, Francesca L'Episcopo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocationMaria Antonietta Di Bella, Francesco Calì, Gregorio Seidita, et al.
BMJ Open|August 9, 2020
Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents' experiences through a multicentre narrative medicine researchLetizia Ragusa, Antonio Crinò, Graziano Grugni, et al.
Frontiers in Pharmacology|April 5, 2024
Low TGF-β1 plasma levels are associated with cognitive decline in Down syndromeMargherita Grasso, Annamaria Fidilio, Francesca L'Episcopo, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteriaGiuseppe Marangi, Stefania Ricciardi, Daniela Orteschi, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndromeVittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, et al.
Pageof 5