Francesco Nicita

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 21

Top Venues

Genes

Brain sciences

Annals of neurology

Movement disorders : official journal of the Movement Disorder Society

This page only lists publications with an associated author ORCID identifier.

Publications

Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, Giacomo Garone, Michaela Veronika Gonfiantini, Davide Vecchio, Lorenzo Sinibaldi, Flaminia Frascarelli, Viola Ceccatelli, Sara Petrillo, Fiorella Piemonte, Gabriele Piccolo, Antonio Novelli, Daniela Longo, Stefano Pro, Adele D'Amico, Enrico Silvio Bertini, Francesco Nicita
Spectrum of ERCC6 -Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes 15 (4) (2024)
Juan Dario Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri, Javeria Raza Alvi, Tipu Sultan, Hamid Galehdari, Gholamreza Shariati, Alihossein Saberi, Lisette Leeuwen, Giovanni Zifarelli, Peter Bauer, Vincent d'Hardemare, Diane Doummar, Emmanuel Roze, Lorena Travaglini, Francesco Nicita, Núria Ojea Ponce, Seyed Mohammadsaleh Zahraei, Lama Alabdi, Abdullah Tamim, Mais O Hashem, Faroug Ababneh, Michelle M Morrow, Cynthia Curry, Allison Tam, Jessica Ruedy, Vikas Bhambhani, Regan Veith, Petter Strømme, Stephanie Efthymiou, Fowzan S Alkuraya, Andrés Moreno De Luca, Lydie Burglen, Henry Houlden, Reza Maroofian
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Juan Dario Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri, Javeria Raza Alvi, Tipu Sultan, Hamid Galehdari, Gholamreza Shariati, Alihossein Saberi, Lisette Leeuwen, Giovanni Zifarelli, Peter Bauer, Vincent d'Hardemare, Diane Doummar, Emmanuel Roze, Lorena Travaglini, Francesco Nicita, Núria Ojea Ponce, Seyed Mohammadsaleh Zahraei, Lama Alabdi, Abdullah Tamim, Mais O Hashem, Faroug Ababneh, Michelle M Morrow, Cynthia Curry, Allison Tam, Jessica Ruedy, Vikas Bhambhani, Regan Veith, Petter Strømme, Stephanie Efthymiou, Fowzan S Alkuraya, Andrés Moreno De Luca, Lydie Burglen, Henry Houlden, Reza Maroofian
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders. Movement disorders : official journal of the Movement Disorder Society (2024)
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, Giacomo Garone, Michaela Veronika Gonfiantini, Davide Vecchio, Lorenzo Sinibaldi, Flaminia Frascarelli, Viola Ceccatelli, Sara Petrillo, Fiorella Piemonte, Gabriele Piccolo, Antonio Novelli, Daniela Longo, Stefano Pro, Adele D'Amico, Enrico Silvio Bertini, Francesco Nicita
Spectrum of ERCC6 -Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes 15 (4) (2024)
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, Giacomo Garone, Michaela Veronika Gonfiantini, Davide Vecchio, Lorenzo Sinibaldi, Flaminia Frascarelli, Viola Ceccatelli, Sara Petrillo, Fiorella Piemonte, Gabriele Piccolo, Antonio Novelli, Daniela Longo, Stefano Pro, Adele D'Amico, Enrico Silvio Bertini, Francesco Nicita
Spectrum of ERCC6 -Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes 15 (4) (2024)
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, Giacomo Garone, Michaela Veronika Gonfiantini, Davide Vecchio, Lorenzo Sinibaldi, Flaminia Frascarelli, Viola Ceccatelli, Sara Petrillo, Fiorella Piemonte, Gabriele Piccolo, Antonio Novelli, Daniela Longo, Stefano Pro, Adele D'Amico, Enrico Silvio Bertini, Francesco Nicita
Spectrum of ERCC6 -Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes 15 (4) (2024)
Francesco Nicita, Lorena Travaglini, Valentina Matteo, Chiara Aiello, Daniela Longo, Antonella Insalaco, Enrico Bertini, Giusi Prencipe
Type I Interferon Signature in NOTCH1-Related Leukoencephalopathy. Annals of neurology (2023)
Vito Luigi Colona, Enrico Silvio Bertini, Maria Cristina Digilio, Adele D'Amico, Antonio Novelli, Stefano Pro, Elisa Pisaneschi, Francesco Nicita
A New Case of Autosomal-Dominant POLR3B -Related Disorder: Widening Genotypic and Phenotypic Spectrum . Brain sciences 13 (11) (2023)
Francesco Nicita, Lorena Travaglini, Valentina Matteo, Chiara Aiello, Daniela Longo, Antonella Insalaco, Enrico Bertini, Giusi Prencipe
Type I IFN signature in NOTCH1-related leukoencephalopathy. Annals of neurology (2023)
Francesco Nicita, Letizia Sabatini, Viola Alesi, Giulia Lucignani, Ester Sallicandro, Antonella Sferra, Enrico Silvio Bertini, Ginevra Zanni, Giuseppe Palumbo
Neurological and Neuroimaging Features of CYB5R3 -Related Recessive Hereditary Methemoglobinemia Type II. Brain sciences 12 (2) (2022)
Salvatore Rossi, Anna Rubegni, Vittorio Riso, Melissa Barghigiani, Maria Teresa Bassi, Roberta Battini, Enrico Silvio Bertini, Cristina Cereda, Ettore Cioffi, Chiara Criscuolo, Beatrice Dal Fabbro, Clemente Dato, Maria Grazia D'Angelo, Antonio Di Muzio, Luca Diamanti, Maria Teresa Dotti, Alessandro Filla, Valeria Gioiosa, Rocco Liguori, Andrea Martinuzzi, Roberto Massa, Andrea Mignarri, Rossana Moroni, Olimpia Musumeci, Francesco Nicita, Ilaria Orologio, Laura Orsi, Elena Pegoraro, Antonio Petrucci, Massimo Plumari, Ivana Ricca, Giovanni Rizzo, Giovanni Ristori, Roberto Rumore, Simone Sampaolo, Marina Scarlato, Marco Seri, Cristina Stefan, Giulia Straccia, Alessandra Tessa, Lorena Travaglini, Rosanna Trovato, Lucia Ulgheri, Giovanni Vazza, Antonio Orlacchio, Gabriella Silvestri, Filippo Maria Santorelli, Mariarosa Anna Beatrice Melone, Carlo Casali
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network. Neurology. Genetics 8 (2) (2022)
Sara Petrillo, Jessica D'Amico, Francesco Nicita, Caterina Torda, Gessica Vasco, Enrico Silvio Bertini, Marco Cappa, Fiorella Piemonte
Antioxidant Response in Human X-Linked Adrenoleukodystrophy Fibroblasts. Antioxidants (Basel, Switzerland) 11 (11) (2022)
Francesco Nicita, Fabrizia Stregapede, Federica Deodato, Simone Pizzi, Simone Martinelli, Daria Pagliara, Chiara Aiello, Francesca Cumbo, Fiorella Piemonte, Jessica D'Amico, Stefano Pro, Daniela Longo, Silvia Genovese, Tartaglia Marco, Maria L Escolar, Enrico Bertini, Lorena Travaglini
"Atypical" Krabbe disease in two siblings harboring biallelic GALC mutations including a deep intronic variant. European journal of human genetics : EJHG 30 (8) (2022)
Andrea Diociaiuti, Diego Martinelli, Francesco Nicita, Claudia Cesario, Elisa Pisaneschi, Marina Macchiaiolo, Sabrina Rossi, Angelo Giuseppe Condorelli, Giovanna Zambruno, May El Hachem
Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization. Genes 12 (3) (2021)
Francesco Nicita, Lorena Travaglini, Francesco Bombelli, Michele Tosi, Stefano Pro, Enrico Silvio Bertini, Adele D'Amico
Novel SEPSECS Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case Report. Neurology. Genetics 8 (2) (2021)
Francesco Nicita, Chiara Aiello, Gessica Vasco, Massimiliano Valeriani, Fabrizia Stregapede, Andrea Sancesario, Michela Armando, Enrico Bertini
Expanding the Clinical and Mutational Spectrum of the PLP1-Related Hypomyelination of Early Myelinated Structures (HEMS). Brain sciences 11 (1) (2021)
Francesco Nicita, Monia Ginevrino, Lorena Travaglini, Stefano D'Arrigo, Giovanna Zorzi, Renato Borgatti, Gaetano Terrone, Michela Catteruccia, Gessica Vasco, Vesna Brankovic, Sabrina Siliquini, Silvia Romano, Chiara Veredice, Marina Pedemonte, Michelina Armando, Donatella Lettori, Fabrizia Stregapede, Luca Bosco, Antonella Sferra, Valeria Tessarollo, Ludovica Pasca, Giovanni Ristori, Enrico Bertini, Enza Maria Valente, Ginevra Zanni
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders. Journal of medical genetics 58 (7) (2020)
Antonella Sferra, Francesco Nicita, Enrico Silvio Bertini
Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases. International journal of molecular sciences 21 (19) (2020)
Francesco Nicita, Federica Graziola, Federico Vigevano, Enrico Bertini, Alessandro Capuano
An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype. Acta neurologica Belgica 119 (4) (2019)
Fabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, Vivian Pedigone Cintra, Emanuele Bellacchio, Luca Bosco, Paolo Alfieri, Stefano Pro, Stephan Zuchner, Enrico Bertini, Francesco Nicita
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clinical genetics 97 (3) (2019)
Francesco Nicita, Fabrizia Stregapede, Alessandra Tessa, Maria Teresa Bassi, Aleksandra Jezela-Stanek, Guido Primiano, Antonio Pizzuti, Melissa Barghigiani, Marta Nardella, Ginevra Zanni, Serenella Servidei, Guja Astrea, Elena Panzeri, Cristina Maghini, Luciana Losito, Rafal Ploski, Piotr Gasperowicz, Filippo Maria Santorelli, Enrico Bertini, Lorena Travaglini
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants. Journal of neurology 266 (11) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Francesco Nicita