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Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|April 12, 2014
Complications of native arteriovenous fistula: the role of color Doppler ultrasonographyBianca Visciano, Eleonora Riccio, Vincenzo De Falco, et al.
Gene|July 31, 2025
Investigating the role of a novel hemizygous FAAH2 variant in neurological and metabolic disordersMirella Vinci, Donatella Greco, Simone Treccarichi, et al.
International Journal of Environmental Research and Public Health|September 10, 2021
Implementation of Sample Pooling Procedure Using a Rapid SARS-CoV-2 Diagnostic Real-Time PCR Test Performed Prior to Hospital Admission of People with Intellectual DisabilitiesAntonino Musumeci, Mirella Vinci, Francesca L'Episcopo, et al.
Gene|November 9, 2025
Unravelling the role of Neurotrimin (NTM), a member of the IgLON family, in mild intellectual disability and anxiety-like behaviorsMirella Vinci, Simone Treccarichi, Pinella Failla, et al.
European Journal of Medical Genetics|November 11, 2008
Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGHAdriana Lo-Castro, Grazia Giana, Marco Fichera, et al.
Updates in Surgery|March 7, 2020
Safety of aortic aneurysm repair 8 weeks after percutaneous coronary intervention for coronary artery disease: a cohort studyVito A Mannacio, Luigi Mannacio, Mario Monaco, et al.
Journal of Musculoskeletal & Neuronal Interactions|December 3, 2020
Possible implication of undescribed SMN1-SMN2 genotype in chronic EMG-pattern of SMA with transitory acute denervationGirolamo A Vitello, Francesco Calì, Mirella Vinci, et al.
Scientific Reports|July 9, 2024
A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disabilityMirella Vinci, Simone Treccarichi, Rosanna Galati Rando, et al.
International Journal of Molecular Sciences|May 13, 2026
A De Novo <i>USP24</i> Variant as a Candidate Driver in a Neurodevelopmental Disorder: Insights from Trio-Based Whole-Exome SequencingMirella Vinci, Antonino Musumeci, Simone Treccarichi, et al.
Medicina (Kaunas, Lithuania)|July 30, 2025
Clinical Application of a Customized Gene Panel for Identifying Autism Spectrum Disorder-Associated VariantsVittoria Greco, Donatella Greco, Simone Treccarichi, et al.
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