The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives
Citrigno, Luigi, Muglia, Maria, Qualtieri, Antonio, Spadafora, Patrizia, Cavalcanti, Francesca, Pioggia, Giovanni, Cerasa, Antonio
Published in International journal of molecular sciences (12.08.2020)
Published in International journal of molecular sciences (12.08.2020)
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Journal Article
An ELOVL2-Based Epigenetic Clock for Forensic Age Prediction: A Systematic Review
Paparazzo, Ersilia, Lagani, Vincenzo, Geracitano, Silvana, Citrigno, Luigi, Aceto, Mirella Aurora, Malvaso, Antonio, Bruno, Francesco, Passarino, Giuseppe, Montesanto, Alberto
Published in International journal of molecular sciences (23.01.2023)
Published in International journal of molecular sciences (23.01.2023)
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A Novel Homozygous Variant in DYSF Gene Is Associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B
Spadafora, Patrizia, Qualtieri, Antonio, Cavalcanti, Francesca, Di Palma, Gemma, Gallo, Olivier, De Benedittis, Selene, Cerantonio, Annamaria, Citrigno, Luigi
Published in International journal of molecular sciences (11.08.2022)
Published in International journal of molecular sciences (11.08.2022)
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Journal Article
The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions
Cerantonio, Annamaria, Citrigno, Luigi, Greco, Beatrice Maria, De Benedittis, Selene, Passarino, Giuseppe, Maletta, Raffaele, Qualtieri, Antonio, Montesanto, Alberto, Spadafora, Patrizia, Cavalcanti, Francesca
Published in International journal of molecular sciences (01.06.2024)
Published in International journal of molecular sciences (01.06.2024)
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Journal Article
Thymic function and survival at advance ages in nursing home residents from Southern Italy
Paparazzo, Ersilia, Geracitano, Silvana, Lagani, Vincenzo, Citrigno, Luigi, Bartolomeo, Denise, Aceto, Mirella Aurora, Bruno, Francesco, Maletta, Raffaele, Passarino, Giuseppe, Montesanto, Alberto
Published in Immunity & ageing (10.04.2023)
Published in Immunity & ageing (10.04.2023)
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Journal Article
A Blood-Based Molecular Clock for Biological Age Estimation
Paparazzo, Ersilia, Geracitano, Silvana, Lagani, Vincenzo, Bartolomeo, Denise, Aceto, Mirella Aurora, D'Aquila, Patrizia, Citrigno, Luigi, Bellizzi, Dina, Passarino, Giuseppe, Montesanto, Alberto
Published in Cells (Basel, Switzerland) (21.12.2022)
Published in Cells (Basel, Switzerland) (21.12.2022)
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Journal Article
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report
Sprovieri, Teresa, Ungaro, Carmine, Sivo, Serena, Quintiliani, Michela, Contaldo, Ilaria, Veredice, Chiara, Citrigno, Luigi, Muglia, Maria, Cavalcanti, Francesca, Cavallaro, Sebastiano, Mercuri, Eugenio, Battaglia, Domenica
Published in BMC medical genetics (12.03.2019)
Published in BMC medical genetics (12.03.2019)
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Journal Article
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis
Sproviero, William, La Bella, Vincenzo, Mazzei, Rosalucia, Valentino, Paola, Rodolico, Carmelo, Simone, Isabella Laura, Logroscino, Giancarlo, Ungaro, Carmine, Magariello, Angela, Patitucci, Alessandra, Tedeschi, Gioacchino, Spataro, Rossella, Condino, Francesca, Bono, Francesco, Citrigno, Luigi, Monsurrò, Maria Rosaria, Muglia, Maria, Gambardella, Antonio, Quattrone, Aldo, Conforti, Francesca Luisa
Published in Neurobiology of aging (01.04.2012)
Published in Neurobiology of aging (01.04.2012)
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Journal Article
Alzheimer’s disease as a viral disease: Revisiting the infectious hypothesis
Bruno, Francesco, Abondio, Paolo, Bruno, Rossella, Ceraudo, Leognano, Paparazzo, Ersilia, Citrigno, Luigi, Luiselli, Donata, Bruni, Amalia C., Passarino, Giuseppe, Colao, Rosanna, Maletta, Raffaele, Montesanto, Alberto
Published in Ageing research reviews (01.11.2023)
Published in Ageing research reviews (01.11.2023)
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Journal Article
Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies
Citrigno, Luigi, Qualtieri, Antonio, Cerantonio, Annamaria, De Benedittis, Selene, Gallo, Olivier, Di Palma, Gemma, Spadafora, Patrizia, Cavalcanti, Francesca
Published in Journal of the neurological sciences (15.02.2024)
Published in Journal of the neurological sciences (15.02.2024)
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Journal Article
LC‐MALDI‐TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines
De Benedittis, Selene, Gaspari, Marco, Magariello, Angela, Spadafora, Patrizia, Citrigno, Luigi, Romeo, Nelide, Qualtieri, Antonio
Published in Journal of mass spectrometry. (01.05.2021)
Published in Journal of mass spectrometry. (01.05.2021)
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Journal Article
A new CYS1678TYR mutation responsible of LGMD2B identified in a family from Southern Italy
Spadafora, Patrizia, Qualtieri, Antonio, Cavalcanti, Francesca, Lanza, Pierluigi, Gallo, Olivier, Di Palma, Gemma, Citrigno, Luigi
Published in Journal of the neurological sciences (01.10.2021)
Published in Journal of the neurological sciences (01.10.2021)
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MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh
De Benedittis, Selene, Spadafora, Patrizia, Gaspari, Marco, Qualtieri, Gabriele, Gallo, Olivier, Di Palma, Gemma, Cavalcanti, Francesca, Citrigno, Luigi, Qualtieri, Antonio
Published in Clinical chemistry and laboratory medicine (27.11.2023)
Published in Clinical chemistry and laboratory medicine (27.11.2023)
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Journal Article
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes
Ferraroli, Elisabetta, Perulli, Marco, Veredice, Chiara, Contaldo, Ilaria, Quintiliani, Michela, Ricci, Martina, Venezia, Ilaria, Citrigno, Luigi, Qualtieri, Antonio, Spadafora, Patrizia, Cavalcanti, Francesca, Battaglia, Domenica Immacolata
Published in Pediatric neurology (01.07.2022)
Published in Pediatric neurology (01.07.2022)
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Journal Article
Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease
Cerantonio, Annamaria, De Benedittis, Selene, Muglia, Maria, Spadafora, Patrizia, Cavalcanti, Francesca, Lanza, Pierluigi, Gallo, Olivier, Di Palma, Gemma, Romeo, Nelide, Bagalà, Angelo, Mazzei, Rosalucia, Propato, Flavia, Consoli, Domenico, Cerasa, Antonio, Qualtieri, Antonio, Citrigno, Luigi
Published in Journal of the neurological sciences (01.10.2021)
Published in Journal of the neurological sciences (01.10.2021)
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Journal Article
High-throughput sequencing of two populations of extracellular vesicles provides an mRNA signature that can be detected in the circulation of breast cancer patients
Conley, Andrew, Minciacchi, Valentina R., Lee, Dhong Hyun, Knudsen, Beatrice S., Karlan, Beth Y., Citrigno, Luigi, Viglietto, Giuseppe, Tewari, Muneesh, Freeman, Michael R., Demichelis, Francesca, Di Vizio, Dolores
Published in RNA biology (04.03.2017)
Published in RNA biology (04.03.2017)
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Journal Article
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene
Manna, Ida, Mumoli, Laura, Labate, Angelo, Citrigno, Luigi, Ferlazzo, Edoardo, Aguglia, Umberto, Quattrone, Aldo, Gambardella, Antonio
Published in Epilepsy research (01.03.2014)
Published in Epilepsy research (01.03.2014)
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Journal Article
ALS and CHARGE syndrome: a clinical and genetic study
Ungaro, Carmine, Citrigno, Luigi, Trojsi, Francesca, Sprovieri, Teresa, Gentile, Giulia, Muglia, Maria, Monsurrò, Maria Rosaria, Tedeschi, Gioacchino, Cavallaro, Sebastiano, Conforti, Francesca Luisa
Published in Acta neurologica Belgica (01.12.2018)
Published in Acta neurologica Belgica (01.12.2018)
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Journal Article
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia
Magariello, Angela, Tortorella, Carla, Citrigno, Luigi, Patitucci, Alessandra, Tortelli, Rosanna, Mazzei, Rosalucia, Conforti, Francesca Luisa, Ungaro, Carmine, Sproviero, William, Gambardella, Antonio, Muglia, Maria
Published in Muscle & nerve (01.06.2012)
Published in Muscle & nerve (01.06.2012)
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Journal Article
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia
McCorquodale III, DS, Ozomaro, U, Huang, J, Montenegro, G, Kushman, A, Citrigno, L, Price, J, Speziani, F, Pericak-Vance, MA, Züchner, S
Published in Clinical genetics (01.06.2011)
Published in Clinical genetics (01.06.2011)
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