Pio d'Adamo
Università degli Studi di Trieste
H-index: 43
Europe-Italy
Top articles of Pio d'Adamo
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity | Andrea Balduit Anna Monica Bianco Alessandro Mangogna Anna Maria Zicari Lucia Leonardi | 2023/5/25 | |
22 ALTERED ANTIGEN PROCESSING AND PRESENTATION PATHWAY IN INTESTINAL EPITHELIAL CELLS IS THE TRIGGER OF CELIAC DISEASE INFLAMMATION. | Gastroenterology | Luigina De Leo Adamo Pio d'Adamo Sara Patrizi Alessia Pin Fabiana Ziberna | 2023/5/1 |
Circular RNAs Could Encode Unique Proteins and Affect Cancer Pathways | Biology | Francesca Crudele Nicoletta Bianchi Anna Terrazzan Pietro Ancona Antonio Frassoldati | 2023/3/24 |
Haploinsufficiency as a foreground Pathomechanism of Poirer-Bienvenu syndrome and novel insights underlying the phenotypic continuum of CSNK2B-associated disorders | Genes | Mariateresa Di Stazio Caterina Zanus Flavio Faletra Alessia Pesaresi Ilaria Ziccardi | 2023/1/18 |
Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of … | HLA | Chiara Magri Eleonora Marchina Emanuele Sansone Adamo Pio D'Adamo Stefania Cappellani | 2023/12 |
A loss‐of‐function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa | Experimental Dermatology | Ana Sofia Lima Estevao de Oliveira Roberta Cardoso de Siqueira Cécile Nait‐Meddour Paola Maura Tricarico Ronald Moura | 2023/11 |
Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis | Elena Maria Nardacchione Paola Maura Tricarico Ronald Moura Adamo Pio d’Adamo Ayshath Thasneem | 2023/12/26 | |
What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study | Genes | Anna Monica Bianco Giulia Ragusa Valentina Di Carlo Flavio Faletra Mariateresa Di Stazio | 2022/10/27 |
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme | haematologica | Roberta Bottega Antonio Marzollo Maddalena Marinoni Emmanouil Athanasakis Ilaria Persico | 2022/3/3 |
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis | Molecular Genetics & Genomic Medicine | Ilaria Persico Agnese Feresin Michela Faleschini Giorgia Fontana Fabio Sirchia | 2022/6 |
MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype | Journal of Pediatric Gastroenterology and Nutrition | Lorenza Matarazzo Anna Monica Bianco Emmanouil Athanasakis Marco Serveres Paola Francalanci | 2022/5/1 |
Incidence of Congenital Clubfoot: Preliminary Data from Italian CeDAP Registry | International Journal of Environmental Research and Public Health | Daniela Dibello Lucio Torelli Valentina Di Carlo Adamo Pio d’Adamo Flavio Faletra | 2022/4/29 |
A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis | Frontiers in Immunology | Paola Maura Tricarico Rossella Gratton Carlos André dos Santos-Silva Ronald Rodrigues de Moura Blendi Ura | 2022/12/5 |
The genetic diagnosis of ultrarare DEEs: an ongoing challenge | Genes | Luciana Musante Paola Costa Caterina Zanus Flavio Faletra Flora M Murru | 2022/3/12 |
Whole-genome methylation study of congenital lung malformations in children | Frontiers in Oncology | Sara Patrizi Federica Pederiva Adamo Pio d’Adamo | 2021/6/28 |
Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique | PLoS One | Mariateresa Di Stazio Nicola Foschi Emmanouil Athanasakis Paolo Gasparini Adamo Pio d’Adamo | 2021/3/5 |
Plant antimicrobial peptides as potential tool for topic treatment of hidradenitis suppurativa | Carlos André dos Santos-Silva Paola Maura Tricarico Lívia Maria Batista Vilela Ricardo Salas Roldan-Filho Vinícius Costa Amador | 2021/12/13 | |
Impact of methylmercury and other heavy metals exposure on neurocognitive function in children aged 7 years: Study protocol of the follow-up | Journal of Epidemiology | Liza Vecchi Brumatti Valentina Rosolen Marika Mariuz Elisa Piscianz Erica Valencic | 2021/2/5 |
Genome-wide profiling and identification of Single Nucleotide Polymorphisms (SNPs) relevant to susceptibility to neurodevelopmental disorders | Public Health Toxicology | I Fragkiadoulaki V Rosolen P d’Adamo E Athanasakis S Cappellani | 2021/9/27 |
Could the MED13 mutations manifest as a Kabuki‐like syndrome? | American Journal of Medical Genetics Part A | Laura De Nardi Flavio Faletra Adamo Pio D'Adamo Anna Monica Rosaria Bianco Emmanouil Athanasakis | 2021/2 |
