CITRIGNO, LUIGI
CITRIGNO, LUIGI
Istituto per la Ricerca e l'Innovazione Biomedica - IRIB - Sede Secondaria Cosenza
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
Alzheimer's Disease as A Viral Infectious Disease: Revisiting the Infectious Hypothesis
2023 Bruno, Francesco; Abondio, Paolo; Bruno, Rossella; Ceraudo, Leognano; Pararazzo, Ersilia; Citrigno, Luigi; Luiselli, Donata; C Bruni, Amalia; Passarino, Giuseppe; Colao, Rosanna; Maletta, Raffaele; Montesanto, Alberto
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review
2023 Paparazzo, Ersilia; Lagani, Vincenzo; Geracitano, Silvana; Citrigno, Luigi; Aurora Aceto, Mirella; Malvaso, Antonio; Bruno, Francesco; Passarino, Giuseppe; Montesanto, Alberto
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
Thymic function and survival at advance ages in nursing home residents from Southern Italy
2023 Paparazzo, Ersilia; Geracitano, Silvana; Lagani, Vincenzo; Citrigno, Luigi; Bartolomeo, Denise; Aurora Aceto, Mirella; Bruno, Francesco; Maletta, Raffaele; Passarino, Giuseppe; Montesanto, Alberto
A Blood-Based Molecular Clock for Biological Age Estimation
2022 Paparazzo, Ersilia; Geracitano, Silvana; Lagani, Vincenzo; Bartolomeo, Denise; Aurora Aceto, Mirella; D'Aquila, Patrizia; Citrigno, Luigi; Bellizzi, Dina; Passarino, Giuseppe; Montesanto, Alberto
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
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy
2022 Spadafora, Patrizia; Citrigno, Luigi; Cavalcanti, Francesca; DI PALMA, Gemma; Gallo, Olivier; Qualtieri, Antonio
Characterizing Fractal Genetic Variation in the Human Genome from the Hapmap Project
2022 Borri, A; Cerasa, A; Tonin, P; Citrigno, L; Porcaro, C
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
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY
2021 Spadafora, Patrizia; Qualtieri, Antonio; Cavalcanti, Francesca; Lanza, Pierluigi; Gallo, Olivier; DI PALMA, Gemma; Citrigno, Luigi
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
A 71-nucleotide Deletion in the Periaxin Gene in an Italian Patient With Late-Onset Slowly Progressive Demyelinating CMT
2020 Citrigno, Luigi; Zoccolella, Stefano; Lastella, Patrizia; Laura Simone, Isabella; Muglia, Maria
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
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report
2019 Sprovieri, Teresa; Ungaro, Carmine; Sivo, Serena; Quintiliani, Michela; Contaldo, Laria; Veredice, Chiara; Citrigno, Luigi; Muglia, Maria; Cavalcanti, Francesca; Cavallaro, Sebastiano; Maria Mercuri, Eugenio; Battaglia, Domenica
Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease.
2019 Francesca Cavalcanti; Valentina La Cognata; Marta Bellofatto; Chiara Criscuolo; Anna De Rosa; Giuseppe De Michele; Luigi Citrigno
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Alzheimer's Disease as A Viral Infectious Disease: Revisiting the Infectious Hypothesis | 1-gen-2023 | Bruno, Francesco; Abondio, Paolo; Bruno, Rossella; Ceraudo, Leognano; Pararazzo, Ersilia; Citrigno, Luigi; Luiselli, Donata; C Bruni, Amalia; Passarino, Giuseppe; Colao, Rosanna; Maletta, Raffaele; Montesanto, Alberto | |
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review | 1-gen-2023 | Paparazzo, Ersilia; Lagani, Vincenzo; Geracitano, Silvana; Citrigno, Luigi; Aurora Aceto, Mirella; Malvaso, Antonio; Bruno, Francesco; Passarino, Giuseppe; Montesanto, Alberto | |
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 | |
Thymic function and survival at advance ages in nursing home residents from Southern Italy | 1-gen-2023 | Paparazzo, Ersilia; Geracitano, Silvana; Lagani, Vincenzo; Citrigno, Luigi; Bartolomeo, Denise; Aurora Aceto, Mirella; Bruno, Francesco; Maletta, Raffaele; Passarino, Giuseppe; Montesanto, Alberto | |
A Blood-Based Molecular Clock for Biological Age Estimation | 1-gen-2022 | Paparazzo, Ersilia; Geracitano, Silvana; Lagani, Vincenzo; Bartolomeo, Denise; Aurora Aceto, Mirella; D'Aquila, Patrizia; Citrigno, Luigi; Bellizzi, Dina; Passarino, Giuseppe; Montesanto, Alberto | |
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 | |
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy | 1-gen-2022 | Spadafora, Patrizia; Citrigno, Luigi; Cavalcanti, Francesca; DI PALMA, Gemma; Gallo, Olivier; Qualtieri, Antonio | |
Characterizing Fractal Genetic Variation in the Human Genome from the Hapmap Project | 1-gen-2022 | Borri, A; Cerasa, A; Tonin, P; Citrigno, L; Porcaro, C | |
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 | |
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY | 1-gen-2021 | Spadafora, Patrizia; Qualtieri, Antonio; Cavalcanti, Francesca; Lanza, Pierluigi; Gallo, Olivier; DI PALMA, Gemma; Citrigno, Luigi | |
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 | |
A 71-nucleotide Deletion in the Periaxin Gene in an Italian Patient With Late-Onset Slowly Progressive Demyelinating CMT | 1-gen-2020 | Citrigno, Luigi; Zoccolella, Stefano; Lastella, Patrizia; Laura Simone, Isabella; Muglia, Maria | |
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 | |
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report | 1-gen-2019 | Sprovieri, Teresa; Ungaro, Carmine; Sivo, Serena; Quintiliani, Michela; Contaldo, Laria; Veredice, Chiara; Citrigno, Luigi; Muglia, Maria; Cavalcanti, Francesca; Cavallaro, Sebastiano; Maria Mercuri, Eugenio; Battaglia, Domenica | |
Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease. | 1-gen-2019 | Francesca Cavalcanti; Valentina La Cognata; Marta Bellofatto; Chiara Criscuolo; Anna De Rosa; Giuseppe De Michele; Luigi Citrigno |