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Journal of Pediatric Genetics|September 15, 2016
SMN1 gene copy number analyses for SMA healthy carriers in Italian populationAlessandra Patitucci, Angela Magariello, Carmine Ungaro, et al.
Acta Neurologica Belgica|March 20, 2012
Phenotypic heterogeneity in hereditary motor neuropathy type V: a new case report seriesManuela Pennisi, Alberto Raggi, Rita Barone, et al.
Immunity & Ageing : I & A|April 10, 2023
Thymic function and survival at advance ages in nursing home residents from Southern ItalyErsilia Paparazzo, Silvana Geracitano, Vincenzo Lagani, et al.
Cells|January 8, 2023
A Blood-Based Molecular Clock for Biological Age EstimationErsilia Paparazzo, Silvana Geracitano, Vincenzo Lagani, et al.
International Journal of Molecular Sciences|June 19, 2024
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future DirectionsAnnamaria Cerantonio, Luigi Citrigno, Beatrice Maria Greco, et al.
Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Genes|June 26, 2025
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer's DiseaseAnnamaria Cerantonio, Beatrice Maria Greco, Luigi Citrigno, et al.
BMC Medical Genetics|March 15, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case reportTeresa Sprovieri, Carmine Ungaro, Serena Sivo, et al.
Ageing Research Reviews|September 13, 2023
Alzheimer's disease as a viral disease: Revisiting the infectious hypothesisFrancesco Bruno, Paolo Abondio, Rossella Bruno, et al.
Pediatric Neurology|May 31, 2022
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related PhenotypesElisabetta Ferraroli, Marco Perulli, Chiara Veredice, et al.
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