Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Luigi Chiriatti"'
Autor:
Carlo Brighi, Federica Cordella, Luigi Chiriatti, Alessandro Soloperto, Silvia Di Angelantonio
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Recent progress in tissue engineering has led to increasingly complex approaches to investigate human neurodegenerative diseases in vitro, such as Alzheimer’s disease, aiming to provide more functional and physiological models for the study of thei
Externí odkaz:
https://doaj.org/article/20fc2711ba75430093baae274ec4774f
Autor:
Manuela Priolo, Erika Zara, Francesca Clementina Radio, Andrea Ciolfi, Francesca Spadaro, Emanuele Bellacchio, Cecilia Mancini, Francesca Pantaleoni, Viviana Cordeddu, Luigi Chiriatti, Marcello Niceta, Emilio Africa, Corrado Mammì, Daniela Melis, Simona Coppola, Marco Tartaglia
Publikováno v:
European Journal of Human Genetics.
Autor:
Manuela Priolo, Cecilia Mancini, Francesca Clementina Radio, Luigi Chiriatti, Andrea Ciolfi, Camilla Cappelletti, Viviana Cordeddu, Letizia Pintomalli, Alfredo Brusco, Corrado Mammi, Marco Tartaglia
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.
Autor:
Marco Ferilli, Andrea Ciolfi, Lucia Pedace, Marcello Niceta, Francesca Clementina Radio, Simone Pizzi, Evelina Miele, Camilla Cappelletti, Cecilia Mancini, Tiziana Galluccio, Marco Andreani, Maria Iascone, Luigi Chiriatti, Antonio Novelli, Alessia Micalizzi, Marta Matraxia, Lucia Menale, Flavio Faletra, Paolo Prontera, Alba Pilotta, Maria Francesca Bedeschi, Rossella Capolino, Anwar Baban, Marco Seri, Corrado Mammì, Giuseppe Zampino, Maria Cristina Digilio, Bruno Dallapiccola, Manuela Priolo, Marco Tartaglia
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 2163
Background: Inactivating NSD1 mutations causing Sotos syndrome have been previously associated with a specific genome-wide DNA methylation (DNAm) pattern. Sotos syndrome is characterized by phenotypic overlap with other overgrowth syndromes, and a de
Autor:
Manuela Priolo, Cecilia Mancini, Simone Pizzi, Luigi Chiriatti, Francesca Clementina Radio, Viviana Cordeddu, Letizia Pintomalli, Corrado Mammì, Bruno Dallapiccola, Marco Tartaglia
Publikováno v:
Genes; Volume 13; Issue 5; Pages: 889
Objective: The co-occurrence of pathogenic variants has emerged as a relatively common finding underlying complex phenotypes. Here, we used whole-exome sequencing (WES) to solve an unclassified multisystem clinical presentation. Patients and Methods:
Autor:
Luigi Chiriatti, Federica Cordella, Alessandro Soloperto, Carlo Brighi, Silvia Di Angelantonio
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Frontiers in Neuroscience
Frontiers in Neuroscience
Recent progress in tissue engineering has led to increasingly complex approaches to investigate human neurodegenerative diseases in vitro, such as Alzheimer’s disease, aiming to provide more functional and physiological models for the study of thei
Autor:
Luisa Del Giudice, Luigi Chiriatti
Publikováno v:
Journal of American Folklore. 112:96-99
Autor:
Marcello Sorce Keller, Sandra Tarantino, Eugenio Imbriani, G Plastino, Elisa Miranda, Luigi Chiriatti, Ellen Harold, Alan Lomax, Diego Carpitella, Mario Spagna, Franco T. Tommasi, Gianni De Santis, Luisa Del Giudice
Publikováno v:
Yearbook for Traditional Music. 35:241