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Donatella Greco

Showing results (11-20 of 41) with videos related to

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Research in Developmental Disabilities|January 26, 2021
Clinical management of individuals with Intellectual Disability: The outbreak of Covid-19 pandemic as experienced in a clinical and research center Research in Developmental DisabilitiesSerafino Buono, Marinella Zingale, Santina Città, et al.
Medicina (Kaunas, Lithuania)|June 2, 2021
Prader-Willi Syndrome with Angelman Syndrome in the OffspringDonatella Greco, Luigi Vetri, Letizia Ragusa, et al.
Current Issues in Molecular Biology|February 23, 2024
Next Generation Sequencing and Electromyography Reveal the Involvement of the <i>P2RX6</i> Gene in MyopathyMirella Vinci, Girolamo Aurelio Vitello, Donatella Greco, et al.
Molecular Genetics & Genomic Medicine|July 5, 2022
Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 geneMirella Vinci, Petri Kursula, Donatella Greco, et al.
Biomedicines|January 28, 2026
Dysregulation of miRNAs in Sicilian Patients with Autism Spectrum DisorderMichele Salemi, Francesca A Schillaci, Maria Grazia Salluzzo, et al.
Gene|September 16, 2024
PPP2R5E: New gene potentially involved in specific learning disorders and myopathyAntonino Musumeci, Mirella Vinci, Iris Verbinnen, et al.
Genes|January 8, 2025
Exploring the Role of <i>FICD</i>, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic DisordersMirella Vinci, Donatella Greco, Maria Grazia Figura, et al.
Gene|October 15, 2013
Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosisLucia Grillo, Donatella Greco, Rosa Pettinato, et al.
Human Genetics|January 19, 2019
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophyMarco Fichera, Pinella Failla, Lucia Saccuzzo, et al.
Biomedicines|July 27, 2024
Transcriptome Study in Sicilian Patients with Autism Spectrum DisorderMichele Salemi, Francesca A Schillaci, Giuseppe Lanza, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Research in Developmental Disabilities|January 26, 2021
Clinical management of individuals with Intellectual Disability: The outbreak of Covid-19 pandemic as experienced in a clinical and research center Research in Developmental DisabilitiesSerafino Buono, Marinella Zingale, Santina Città, et al.
Medicina (Kaunas, Lithuania)|June 2, 2021
Prader-Willi Syndrome with Angelman Syndrome in the OffspringDonatella Greco, Luigi Vetri, Letizia Ragusa, et al.
Current Issues in Molecular Biology|February 23, 2024
Next Generation Sequencing and Electromyography Reveal the Involvement of the <i>P2RX6</i> Gene in MyopathyMirella Vinci, Girolamo Aurelio Vitello, Donatella Greco, et al.
Molecular Genetics & Genomic Medicine|July 5, 2022
Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 geneMirella Vinci, Petri Kursula, Donatella Greco, et al.
Biomedicines|January 28, 2026
Dysregulation of miRNAs in Sicilian Patients with Autism Spectrum DisorderMichele Salemi, Francesca A Schillaci, Maria Grazia Salluzzo, et al.
Gene|September 16, 2024
PPP2R5E: New gene potentially involved in specific learning disorders and myopathyAntonino Musumeci, Mirella Vinci, Iris Verbinnen, et al.
Genes|January 8, 2025
Exploring the Role of <i>FICD</i>, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic DisordersMirella Vinci, Donatella Greco, Maria Grazia Figura, et al.
Gene|October 15, 2013
Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosisLucia Grillo, Donatella Greco, Rosa Pettinato, et al.
Human Genetics|January 19, 2019
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophyMarco Fichera, Pinella Failla, Lucia Saccuzzo, et al.
Biomedicines|July 27, 2024
Transcriptome Study in Sicilian Patients with Autism Spectrum DisorderMichele Salemi, Francesca A Schillaci, Giuseppe Lanza, et al.
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