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Biomedicines|November 27, 2024
Exome Profiling Suggests Combined Effect of Myeloperoxidase, Toll-Like Receptors, and Metallopeptidase in Hidradenitis SuppurativaAlessia Azzarà, Ilaria Cassano, Carla Lintas, et al.Biomedicines|August 28, 2025
Identification of Candidate Genes for Endometriosis in a Three-Generation Family with Multiple Affected Members Using Whole-Exome SequencingCarla Lintas, Alessia Azzarà, Vincenzo Panasiti, et al.Mutation Research|May 14, 2016
Different repair kinetic of DSBs induced by mitomycin C in peripheral lymphocytes of obese and normal weight adolescentsAlessia Azzarà, Chiara Pirillo, Caterina Giovannini, et al.Journal of Clinical Medicine|November 13, 2021
Genotype-Phenotype Correlations in Relation to Newly Emerging Monogenic Forms of Autism Spectrum Disorder and Associated Neurodevelopmental Disorders: The Importance of Phenotype Reevaluation after Pangenomic ResultsCarla Lintas, Roberto Sacco, Alessia Azzarà, et al.Genes|May 25, 2024
Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial CancerCarla Lintas, Benedetta Canalis, Alessia Azzarà, et al.Genes|October 27, 2022
Genetic Dysruption of the Histaminergic Pathways: A Novel Deletion at the 15q21.2 locus Associated with Variable Expressivity of Neuropsychiatric DisordersCarla Lintas, Roberto Sacco, Alessia Azzarà, et al.Frontiers in Genetics|May 17, 2017
Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?Veronica Bertini, Alessia Azzarà, Annalisa Legitimo, et al.Genes|February 25, 2023
RADX Gene Variant May Predispose to Familial Asperger SyndromeAlessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, et al.Genes|July 29, 2023
Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual DisabilityCarla Lintas, Angelo Facchiano, Alessia Azzarà, et al.Genes|July 29, 2023
Melkersson-Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?Alessia Azzarà, Ilaria Cassano, Carla Lintas, et al.Pageof 3