Works by D'Adamo, Adamo Pio

Results: 29

Genomic instability in congenital lung malformations in children.

Published in:

Pediatric Surgery International, 2024, v. 40, n. 1, p. 1, doi. 10.1007/s00383-024-05835-5

By:

Rodrigues de Moura, Ronald;
Patrizi, Sara;
Athanasakis, Emmanouil;
Schleef, Jurgen;
Pederiva, Federica;
d'Adamo, Adamo Pio

Publication type:

Article

Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1926

By:

Persico, Ilaria;
Feresin, Agnese;
Faleschini, Michela;
Fontana, Giorgia;
Sirchia, Fabio;
Faletra, Flavio;
La Bianca, Martina;
Suergiu, Sarah;
Morgutti, Marcello;
Maschio, Massimo;
D'Adamo, Adamo Pio;
Raraigh, Karen S.;
Savoia, Anna;
Bottega, Roberta

Publication type:

Article

A loss‐of‐function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa.

Published in:

Experimental Dermatology, 2023, v. 32, n. 11, p. 1935, doi. 10.1111/exd.14919

By:

de Oliveira, Ana Sofia Lima Estevao;
de Siqueira, Roberta Cardoso;
Nait‐Meddour, Cécile;
Tricarico, Paola Maura;
Moura, Ronald;
Agrelli, Almerinda;
d'Adamo, Adamo Pio;
Jamain, Stéphane;
Crovella, Sergio;
de Fátima Medeiros Brito, Maria;
Boniotto, Michele;
Brandão, Lucas André Cavalcanti

Publication type:

Article

Plant Antimicrobial Peptides as Potential Tool for Topic Treatment of Hidradenitis Suppurativa.

Published in:

Frontiers in Microbiology, 2021, v. 12, p. 1, doi. 10.3389/fmicb.2021.795217

By:

Santos-Silva, Carlos André dos;
Tricarico, Paola Maura;
Vilela, Lívia Maria Batista;
Roldan-Filho, Ricardo Salas;
Amador, Vinícius Costa;
d'Adamo, Adamo Pio;
Rêgo, Mireli de Santana;
Benko-Iseppon, Ana Maria;
Crovella, Sergio

Publication type:

Article

A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis.

Published in:

Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1060547

By:

Tricarico, Paola Maura;
Gratton, Rossella;
André dos Santos-Silva, Carlos;
Rodrigues de Moura, Ronald;
Ura, Blendi;
Sommella, Eduardo;
Campiglia, Pietro;
Del Vecchio, Cecilia;
Moltrasio, Chiara;
Berti, Irene;
D’Adamo, Adamo Pio;
Elsherbini, Ahmed M. A.;
Staudenmaier, Lena;
Chersi, Karin

Publication type:

Article

Genomic instability in congenital lung malformations in children.

Published in:

Pediatric Surgery International, 2024, v. 40, n. 1, p. 1, doi. 10.1007/s00383-024-05835-5

By:

Rodrigues de Moura, Ronald;
Patrizi, Sara;
Athanasakis, Emmanouil;
Schleef, Jurgen;
Pederiva, Federica;
d'Adamo, Adamo Pio

Publication type:

Article

Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset.

Published in:

Cancers, 2019, v. 11, n. 4, p. 483, doi. 10.3390/cancers11040483

By:

Agnoletto, Chiara;
Corrà, Fabio;
Minotti, Linda;
Baldassari, Federica;
Crudele, Francesca;
Cook, William Joseph James;
Di Leva, Gianpiero;
d'Adamo, Adamo Pio;
Gasparini, Paolo;
Volinia, Stefano

Publication type:

Article

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 the HLA‐A*03:01 allele.

Published in:

HLA: Immune Response Genetics, 2023, v. 102, n. 6, p. 707, doi. 10.1111/tan.15157

By:

Magri, Chiara;
Marchina, Eleonora;
Sansone, Emanuele;
D'Adamo, Adamo Pio;
Cappellani, Stefania;
Bonfanti, Carlo;
Terlenghi, Luigina;
Biasiotto, Giorgio;
Zanella, Isabella;
Sala, Emma;
Caruso, Arnaldo;
Lombardo, Massimo;
Gasparini, Paolo;
De Palma, Giuseppe;
Gennarelli, Massimo

Publication type:

Article

High prevalence of rare FBLIM1 gene variants in an Italian cohort of patients with Chronic Non-bacterial Osteomyelitis (CNO).

Published in:

Pediatric Rheumatology, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s12969-020-00447-4

By:

d'Adamo, Adamo Pio;
Bianco, Anna Monica;
Ferrara, Giovanna;
La Bianca, Martina;
Insalaco, Antonella;
Tommasini, Alberto;
Pardeo, Manuela;
Cattalini, Marco;
La Torre, Francesco;
Finetti, Martina;
Alizzi, Clotilde;
Simonini, Gabriele;
Messia, Virginia;
Pastore, Serena;
Cimaz, Rolando;
Gattorno, Marco;
Taddio, Andrea

Publication type:

Article

Neuron‐Derived Extracellular Vesicles miRNA Profiles Identify Children Who Experience Adverse Events after Ketamine Administration for Procedural Sedation.

Published in:

Clinical Pharmacology & Therapeutics, 2025, v. 117, n. 1, p. 174, doi. 10.1002/cpt.3420

By:

Lucafò, Marianna;
Bidoli, Carlotta;
Franzin, Martina;
Eitan, Erez;
Rau, Sara;
Amaddeo, Alessandro;
Fachin, Alice;
d'Adamo, Adamo Pio;
Decorti, Giuliana;
Stocco, Gabriele;
Barbi, Egidio;
Cozzi, Giorgio

Publication type:

Article

Sensitive Detection of Gynecological Cancer Recurrence Using Circulating Tumor DNA and Digital PCR: A Comparative Study with Serum Biochemical Markers.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 22, p. 11997, doi. 10.3390/ijms252211997

By:

Balasan, Nour;
Kharrat, Feras;
Di Lorenzo, Giovanni;
Athanasakis, Emmanouil;
Bianco, Anna Monica;
Conti, Andrea;
Di Stazio, Maria Teresa;
Butera, Giulia;
Cicogna, Stefania;
Mangogna, Alessandro;
Romano, Federico;
Ricci, Giuseppe;
d'Adamo, Adamo Pio

Publication type:

Article

Notch Signaling Regulation in Autoinflammatory Diseases.

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 22, p. 8847, doi. 10.3390/ijms21228847

By:

Gratton, Rossella;
Tricarico, Paola Maura;
d'Adamo, Adamo Pio;
Bianco, Anna Monica;
Moura, Ronald;
Agrelli, Almerinda;
Brandão, Lucas;
Zupin, Luisa;
Crovella, Sergio

Publication type:

Article

Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families.

Published in:

International Journal of Audiology, 2003, v. 42, n. 8, p. 475, doi. 10.3109/14992020309081517

By:

Di Leva, Francesca;
D'Adamo, Adamo Pio;
Strollo, Luciano;
Auletta, Gennaro;
Caravelli, Antonella;
Carella, Massimo;
Mari, Francesca;
Livi, Walter;
Renieri, Alessandra;
Gasparini, Paolo;
D'Urso, Michele;
Marciano, Elio;
Franze, Annamaria

Publication type:

Article

A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 12, p. 1073, doi. 10.1038/sj.ejhg.5201280

By:

Carella, Massimo;
d'Adamo, Adamo Pio;
Grootenboer-Mignot, Sabine;
Vantyghem, Marie C.;
Esposito, Laura;
D'Eustacchio, Angela;
Ficarella, Romina;
Stewart, Gordon W;
Gasparini, Paolo;
Delaunay, Jean;
Iolascon, Achille

Publication type:

Article

Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 585, doi. 10.1038/sj.ejhg.5201009

By:

Rivard, Sylvain R;
Lanzara, Carmela;
Grimard, Doria;
Carella, Massimo;
Simard, Hervey;
Ficarella, Romina;
Simard, Raynald;
D'Adamo, Adamo Pio;
Férec, Claude;
Camaschella, Clara;
Mura, Cathrine;
Roetto, Antonella;
De Braekeleer, Marc;
Bechner, Lucien;
Gasparini, Paolo

Publication type:

Article

Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique.

Published in:

PLoS ONE, 2021, v. 16, n. 3, p. 1, doi. 10.1371/journal.pone.0247603

By:

Di Stazio, Mariateresa;
Foschi, Nicola;
Athanasakis, Emmanouil;
Gasparini, Paolo;
d'Adamo, Adamo Pio

Publication type:

Article

MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype.

Published in:

2022

By:

Matarazzo, Lorenza;
Bianco, Anna Monica;
Athanasakis, Emmanouil;
Serveres, Marco;
Francalanci, Paola;
Cenacchi, Giovanna;
Maggiore, Giuseppe;
D'Adamo, Adamo Pio

Publication type:

journal article

Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity.

Published in:

Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1192690

By:

Balduit, Andrea;
Bianco, Anna Monica;
Mangogna, Alessandro;
Zicari, Anna Maria;
Leonardi, Lucia;
Cinicola, Bianca Laura;
Capponi, Martina;
Tommasini, Alberto;
Agostinis, Chiara;
d'Adamo, Adamo Pio;
Bulla, Roberta

Publication type:

Article

New Tools for Congenital Hyperinsulinism.

Published in:

2021

By:

Da Lozzo, Prisca;
Risso, Francesco Maria;
Schleef, Jürgen;
Sirchia, Fabio;
Sagredini, Raffaella;
Bussani, Rossana;
D'Adamo, Adamo Pio;
Barbi, Egidio;
Tornese, Gianluca

Publication type:

Case Study

Incidence of Congenital Clubfoot: Preliminary Data from Italian CeDAP Registry.

Published in:

International Journal of Environmental Research & Public Health, 2022, v. 19, n. 9, p. 5406, doi. 10.3390/ijerph19095406

By:

Dibello, Daniela;
Torelli, Lucio;
Di Carlo, Valentina;
d'Adamo, Adamo Pio;
Faletra, Flavio;
Mangogna, Alessandro;
Colin, Giulia

Publication type:

Article

Whole-Genome Methylation Study of Congenital Lung Malformations in Children.

Published in:

Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.689833

By:

Patrizi, Sara;
Pederiva, Federica;
d'Adamo, Adamo Pio

Publication type:

Article

A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family.

Published in:

Ophthalmic Genetics, 2013, v. 34, n. 1/2, p. 115, doi. 10.3109/13816810.2012.707273

By:

Faletra, Flavio;
d'Adamo, Adamo Pio;
Pensiero, Stefano;
Athanasakis, Emmanouil;
Catalano, Dario;
Bruno, Irene;
Gasparini, Paolo

Publication type:

Article

Could the MED13 mutations manifest as a Kabuki‐like syndrome?

Published in:

American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 584, doi. 10.1002/ajmg.a.61994

By:

De Nardi, Laura;
Faletra, Flavio;
D'Adamo, Adamo Pio;
Bianco, Anna Monica Rosaria;
Athanasakis, Emmanouil;
Bruno, Irene;
Barbi, Egidio

Publication type:

Article

Does the 1.5 Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 2, p. 461, doi. 10.1002/ajmg.a.34398

By:

Faletra, Flavio;
D'Adamo, Adamo Pio;
Rocca, Maria Santa;
Carrozzi, Marco;
Perrone, Maria Dolores;
Pecile, Vanna;
Gasparini, Paolo

Publication type:

Article

Genotypes and different clinical variants between children and adults in progressive familial intrahepatic cholestasis: a state-of-the-art review.

Published in:

Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03599-2

By:

Vitale, Giovanni;
Sciveres, Marco;
Mandato, Claudia;
d'Adamo, Adamo Pio;
Di Giorgio, Angelo

Publication type:

Article

Dysregulation of Aquaporin-3 and Glyceryl Glucoside Restoring Action in Hidradenitis Suppurativa in Vitro Models.

Published in:

Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2024, v. 58, n. 4, p. 404, doi. 10.33594/000000720

By:

Del Vecchio, Cecilia;
Gratton, Rossella;
Nait-Meddour, Cécile;
Nardacchione, Elena Maria;
Moura, Ronald;
Sommell, Eduardo;
Moltrasio, Chiara;
Valerio Marzano, Angelo;
Ura, Blendi;
Mentino, Donatella;
Boniotto, Michele;
d'Adamo, Adamo Pio;
Calamita, Giuseppe;
Crovella, Sergio;
Tricarico, Paola Maura

Publication type:

Article

Identification of a New Mutation in RSK2 , the Gene for Coffin–Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes.

Published in:

Brain Sciences (2076-3425), 2021, v. 11, n. 8, p. 1105, doi. 10.3390/brainsci11081105

By:

Di Stazio, Mariateresa;
Bigoni, Stefania;
Iuso, Nicola;
Vuch, Josef;
Selvatici, Rita;
Ulivi, Sheila;
d'Adamo, Pio Adamo

Publication type:

Article

Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis.

Published in:

Genes, 2024, v. 15, n. 1, p. 38, doi. 10.3390/genes15010038

By:

Nardacchione, Elena Maria;
Tricarico, Paola Maura;
Moura, Ronald;
d'Adamo, Adamo Pio;
Thasneem, Ayshath;
Suleman, Muhammad;
Marzano, Angelo Valerio;
Crovella, Sergio;
Moltrasio, Chiara

Publication type:

Article

32 Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0120-0

By:

Iossa, Sandra;
Costa, Valerio;
Corvino, Virginia;
Auletta, Gennaro;
Barruffo, Luigi;
Cappellani, Stefania;
Ceglia, Carlo;
Cennamo, Giovanni;
D'Adamo, Adamo Pio;
D'Amico, Alessandra;
Di Paolo, Nilde;
Forte, Raimondo;
Gasparini, Paolo;
Laria, Carla;
Lombardo, Barbara;
Malesci, Rita;
Vitale, Andrea;
Marciano, Elio;
Franzè, Annamaria

Publication type:

Article