Manuela Priolo (M Priolo)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 10

Top Topics

Cross Sectional

Dna Methylation

Health Insurance

Top Venues

International journal of environmental research and public health

Orphanet journal of rare diseases

Journal of clinical medicine

European journal of human genetics : EJHG

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

Publications

T N Huynh, C G Delagrammatikas, L Chiriatti, A Panfili, K Ventarola, L A Menke, M Tartaglia, S A Huisman, Manuela Priolo
Natural history in Malan syndrome: survey of 28 adults and literature review. Orphanet journal of rare diseases 19 (1) (2024)
T N Huynh, C G Delagrammatikas, L Chiriatti, A Panfili, K Ventarola, L A Menke, M Tartaglia, S A Huisman, Manuela Priolo
Natural history in Malan syndrome: survey of 28 adults and literature review. Orphanet journal of rare diseases 19 (1) (2024)
T N Huynh, C G Delagrammatikas, L Chiriatti, A Panfili, K Ventarola, L A Menke, M Tartaglia, S A Huisman, Manuela Priolo
Natural history in Malan syndrome: survey of 28 adults and literature review. Orphanet journal of rare diseases 19 (1) (2024)
Manuela Priolo, Tartaglia Marco
The Right to Ask, the Need to Answer-When Patients Meet Research: How to Cope with Time. International journal of environmental research and public health 20 (5) (2023)
Manuela Priolo, Tartaglia Marco
The Right to Ask, the Need to Answer-When Patients Meet Research: How to Cope with Time. International journal of environmental research and public health 20 (5) (2023)
Manuela Priolo, Tartaglia Marco
The Right to Ask, the Need to Answer-When Patients Meet Research: How to Cope with Time. International journal of environmental research and public health 20 (5) (2023)
Manuela Priolo, Tartaglia Marco
The Right to Ask, the Need to Answer-When Patients Meet Research: How to Cope with Time. International journal of environmental research and public health 20 (5) (2023)
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, Tartaglia Marco
Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European journal of human genetics : EJHG (2023)
Paolo Alfieri, Marina Macchiaiolo, Martina Collotta, Federica Alice Maria Montanaro, Cristina Caciolo, Francesca Cumbo, Paolo Galassi, Filippo Maria Panfili, Fabiana Cortellessa, Marcella Zollino, Maria Accadia, Marco Seri, Tartaglia Marco, Andrea Bartuli, Corrado Mammì, Stefano Vicari, Manuela Priolo
Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome. Journal of clinical medicine 11 (14) (2022)
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, Tartaglia Marco
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants. Genes 13 (11) (2022)