SPADAFORA, PATRIZIA
SPADAFORA, PATRIZIA
Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Cosenza
Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease
2025 Cerantonio, Annamaria; Maria Greco, Beatrice; Citrigno, Luigi; De Benedittis, Selene; Qualtieri, Antonio; Maletta, Raffaele; Montesanto, Alberto; Passarino, Giuseppe; Spadafora, Patrizia; Cavalcanti, Francesca
Genetic variability in ADAM17/TACE is associated with sporadic Alzheimer's disease risk, neuropsychiatric symptoms and cognitive performance on the Rey Auditory Verbal Learning and Clock Drawing Tests
2025 Bruno, Francesco; Aceto, Mirella A; Paparazzo, Ersilia; Arcuri, Domenico; Vozzo, Francesca; Mirante, Serena; Greco, Beatrice M; Serra Cassano, Teresa; Abondio, Paolo; Canterini, Sonia; Malvaso, Antonio; Grecucci, Alessandro; Citrigno, Luigi; Geracitano, Silvana; Spadafora, Patrizia; Puccio, Gianfranco; Frangipane, Francesca; Curcio, Sabrina M; Ferrise, Francesca; Laganà, Valentina; Colao, Rosanna; Passarino, Giuseppe; Bruni, Amalia C; Maletta, Raffaele; Cavalcanti, Francesca; Montesanto, Alberto
Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy
2025 Bruno, Francesco; Spadafora, Patrizia; Veltri, Ida; Cuconati, Mario L.; Condino, Francesca; Cerantonio, Annamaria; De Benedittis, Selene; Greco, Beatrice M.; Di Palma, Gemma; Gallo, Olivier; Citrigno, Luigi; Qualtieri, Antonio; Cundari, Maurizio; Cavalcanti, Francesca
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies
2024 Citrigno, Luigi; Qualtieri, Antonio; Cerantonio, Annamaria; De Benedittis, Selene; Gallo, Olivier; Di Palma, Gemma; Spadafora, Patrizia; Cavalcanti, Francesca
Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype
2024 Qualtieri, Antonio; De Benedittis, Selene; Cerantonio, Annamaria; Citrigno, Luigi; Di Palma, Gemma; Gallo, Olivier; Cavalcanti, Francesca; Spadafora, Patrizia
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions
2024 Cerantonio, A.; Citrigno, L.; Greco, B. M.; De Benedittis, S.; Passarino, G.; Maletta, R.; Qualtieri, A.; Montesanto, A.; Spadafora, P.; Cavalcanti, F.
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis
2023 Cavalcanti, Francesca; Citrigno, Luigi; Spadafora, Patrizia; DE BENEDITTIS, Selene; Gallo, Olivier; DI PALMA, Gemma; Qualtieri, Antonio
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT
2023 Patrizia Spadafora; Luigi Citrigno; Selene De Benedittis; Antonio Qualtieri; Francesca Cavalcanti; Gemma Di Palma; Olivier Gallo; Nelide Romeo
MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh
2023 DE BENEDITTIS, Selene; Spadafora, Patrizia; Gaspari, Marco; I, Gabriele Qualtier; Gallo, Olivier; DI PALMA, Gemma; Cavalcanti, Francesca; Citrigno, Luigi; Qualtieri, Antonio
A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B
2022 Spadafora, Patrizia; Qualtieri, Antonio; Cavalcanti, Francesca; DI PALMA, Gemma; Gallo, Olivier; DE BENEDITTIS, Selene; Cerantonio, Annamaria; Citrigno, Luigi
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes
2022 Ferraroli, Elisabetta; Perulli, Marco; Veredice, Chiara; Contaldo, Ilaria; Quintiliani, Michela; Ricci, Martina; Venezia, Ilaria; Citrigno, Luigi; Qualtieri, Antonio; Spadafora, Patrizia; Cavalcanti, Francesca; Immacolata Battaglia, Domenica
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines
2021 De Benedittis, Selene; Gaspari, Marco; Magariello, Angela; Spadafora, Patrizia; Citrigno, Luigi; Romeo, Nelide; Qualtieri, Antonio
The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives
2020 Citrigno, Luigi; Muglia, Maria; Qualtieri, Antonio; Spadafora, Patrizia; Cavalcanti, Francesca; Pioggia, Giovanni; Cerasa, Antonio
Variants in CAV3, TRIM32 and PSN2 genes suggest an additive effect in the development of dilated cardiomyopathy in a family of south Italy
2019 Spadafora, Patrizia; Romeo, Nelide; Qualtieri, Antonio; DE BENEDITTIS, Selene; De Bartolo, Matteo
IDENTITA' FEMMINILE E SCLEROSI MULTIPLA
2018 Romeo, Nelide; Qualtieri, Antonio; Magariello, Angela; DE BENEDITTIS, Selene; Spadafora, Patrizia
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders
2018 La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano
Tay Sachs in South Italy
2017 Spadafora, Patrizia; Tagarelli, Giuseppe; Romeo, Nelide; Liguori, Maria
FKRP expression in Lymphoblastoid cell lines:a human cellular model to study the impact of the mutations on the protein functionality
2016 Qualtieri, A; Dbosco, ; Abagalà, ; Pspadafora,
G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy
2016 Patrizia Spadafora; Antonio Qualtieri; Nelide Romeo; Angelo Bagalà; Matteo De Bartolo
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy.
2016 Maria Liguori; Giuseppe Tagarelli; Nelide Romeo; Angelo Bagalà; Patrizia Spadafora
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Epigenetic Clocks and Their Prospective Application in the Complex Landscape of Aging and Alzheimer’s Disease | 1-gen-2025 | Cerantonio, Annamaria; Maria Greco, Beatrice; Citrigno, Luigi; De Benedittis, Selene; Qualtieri, Antonio; Maletta, Raffaele; Montesanto, Alberto; Passarino, Giuseppe; Spadafora, Patrizia; Cavalcanti, Francesca | |
| Genetic variability in ADAM17/TACE is associated with sporadic Alzheimer's disease risk, neuropsychiatric symptoms and cognitive performance on the Rey Auditory Verbal Learning and Clock Drawing Tests | 1-gen-2025 | Bruno, Francesco; Aceto, Mirella A; Paparazzo, Ersilia; Arcuri, Domenico; Vozzo, Francesca; Mirante, Serena; Greco, Beatrice M; Serra Cassano, Teresa; Abondio, Paolo; Canterini, Sonia; Malvaso, Antonio; Grecucci, Alessandro; Citrigno, Luigi; Geracitano, Silvana; Spadafora, Patrizia; Puccio, Gianfranco; Frangipane, Francesca; Curcio, Sabrina M; Ferrise, Francesca; Laganà, Valentina; Colao, Rosanna; Passarino, Giuseppe; Bruni, Amalia C; Maletta, Raffaele; Cavalcanti, Francesca; Montesanto, Alberto | |
| Sex and APOE genotype modulate neuropsychological profile and depression in temporal lobe epilepsy | 1-gen-2025 | Bruno, Francesco; Spadafora, Patrizia; Veltri, Ida; Cuconati, Mario L.; Condino, Francesca; Cerantonio, Annamaria; De Benedittis, Selene; Greco, Beatrice M.; Di Palma, Gemma; Gallo, Olivier; Citrigno, Luigi; Qualtieri, Antonio; Cundari, Maurizio; Cavalcanti, Francesca | |
| Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies | 1-gen-2024 | Citrigno, Luigi; Qualtieri, Antonio; Cerantonio, Annamaria; De Benedittis, Selene; Gallo, Olivier; Di Palma, Gemma; Spadafora, Patrizia; Cavalcanti, Francesca | |
| Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype | 1-gen-2024 | Qualtieri, Antonio; De Benedittis, Selene; Cerantonio, Annamaria; Citrigno, Luigi; Di Palma, Gemma; Gallo, Olivier; Cavalcanti, Francesca; Spadafora, Patrizia | |
| The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions | 1-gen-2024 | Cerantonio, A.; Citrigno, L.; Greco, B. M.; De Benedittis, S.; Passarino, G.; Maletta, R.; Qualtieri, A.; Montesanto, A.; Spadafora, P.; Cavalcanti, F. | |
| A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis | 1-gen-2023 | Cavalcanti, Francesca; Citrigno, Luigi; Spadafora, Patrizia; DE BENEDITTIS, Selene; Gallo, Olivier; DI PALMA, Gemma; Qualtieri, Antonio | |
| HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT | 1-gen-2023 | Patrizia Spadafora; Luigi Citrigno; Selene De Benedittis; Antonio Qualtieri; Francesca Cavalcanti; Gemma Di Palma; Olivier Gallo; Nelide Romeo | |
| MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh | 1-gen-2023 | DE BENEDITTIS, Selene; Spadafora, Patrizia; Gaspari, Marco; I, Gabriele Qualtier; Gallo, Olivier; DI PALMA, Gemma; Cavalcanti, Francesca; Citrigno, Luigi; Qualtieri, Antonio | |
| A novel homozygous variant in DYSF gene is associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B | 1-gen-2022 | Spadafora, Patrizia; Qualtieri, Antonio; Cavalcanti, Francesca; DI PALMA, Gemma; Gallo, Olivier; DE BENEDITTIS, Selene; Cerantonio, Annamaria; Citrigno, Luigi | |
| Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes | 1-gen-2022 | Ferraroli, Elisabetta; Perulli, Marco; Veredice, Chiara; Contaldo, Ilaria; Quintiliani, Michela; Ricci, Martina; Venezia, Ilaria; Citrigno, Luigi; Qualtieri, Antonio; Spadafora, Patrizia; Cavalcanti, Francesca; Immacolata Battaglia, Domenica | |
| LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines | 1-gen-2021 | De Benedittis, Selene; Gaspari, Marco; Magariello, Angela; Spadafora, Patrizia; Citrigno, Luigi; Romeo, Nelide; Qualtieri, Antonio | |
| The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives | 1-gen-2020 | Citrigno, Luigi; Muglia, Maria; Qualtieri, Antonio; Spadafora, Patrizia; Cavalcanti, Francesca; Pioggia, Giovanni; Cerasa, Antonio | |
| Variants in CAV3, TRIM32 and PSN2 genes suggest an additive effect in the development of dilated cardiomyopathy in a family of south Italy | 1-gen-2019 | Spadafora, Patrizia; Romeo, Nelide; Qualtieri, Antonio; DE BENEDITTIS, Selene; De Bartolo, Matteo | |
| IDENTITA' FEMMINILE E SCLEROSI MULTIPLA | 1-gen-2018 | Romeo, Nelide; Qualtieri, Antonio; Magariello, Angela; DE BENEDITTIS, Selene; Spadafora, Patrizia | |
| NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders | 1-gen-2018 | La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano | |
| Tay Sachs in South Italy | 1-gen-2017 | Spadafora, Patrizia; Tagarelli, Giuseppe; Romeo, Nelide; Liguori, Maria | |
| FKRP expression in Lymphoblastoid cell lines:a human cellular model to study the impact of the mutations on the protein functionality | 1-gen-2016 | Qualtieri, A; Dbosco, ; Abagalà, ; Pspadafora, | |
| G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy | 1-gen-2016 | Patrizia Spadafora; Antonio Qualtieri; Nelide Romeo; Angelo Bagalà; Matteo De Bartolo | |
| Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. | 1-gen-2016 | Maria Liguori; Giuseppe Tagarelli; Nelide Romeo; Angelo Bagalà; Patrizia Spadafora |