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207 results

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The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II).
Parenti G, Fecarotta S, Alagia M, Attaianese F, Verde A, Tarallo A, Gragnaniello V, Ziagaki A, Guimaraes MJ, Aguiar P, Hahn A, Azevedo O, Donati MA, Kiec-Wilk B, Scarpa M, van der Beek NAME, Del Toro Riera M, Germain DP, Huidekoper H, van den Hout JMP, van der Ploeg AT; and the MetabERN Subnetwork for Lysosomal Disorders. Parenti G, et al. Among authors: verde a. Orphanet J Rare Dis. 2024 Nov 1;19(1):408. doi: 10.1186/s13023-024-03373-w. Orphanet J Rare Dis. 2024. PMID: 39482698 Free PMC article. Review.
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy.
Barretta F, Uomo F, Fecarotta S, Albano L, Crisci D, Verde A, Fisco MG, Gallo G, Dottore Stagna D, Pricolo MR, Alagia M, Terrone G, Rossi A, Parenti G, Ruoppolo M, Mazzaccara C, Frisso G. Barretta F, et al. Among authors: verde a. Genes (Basel). 2023 Apr 26;14(5):980. doi: 10.3390/genes14050980. Genes (Basel). 2023. PMID: 37239340 Free PMC article.
Crohn-Like Colitis in a Young Boy With Hirschsprung Disease.
Verde A, Grammegna A, Petrone E, Mastrominico A, De Brasi D, Mandato C, Ranucci G, Sabbatino MS, Sibilio M, Quitadamo P. Verde A, et al. Inflamm Bowel Dis. 2021 Aug 19;27(9):e112-e113. doi: 10.1093/ibd/izab101. Inflamm Bowel Dis. 2021. PMID: 34003268 No abstract available.
Disc battery ingestion in paediatric age.
Quitadamo P, Caruso F, Del Monaco C, Fiori Nastro F, Verde A, Dolce P, Caldore M, Bucci C. Quitadamo P, et al. Among authors: verde a. Acta Paediatr. 2022 Aug;111(8):1615-1620. doi: 10.1111/apa.16359. Epub 2022 Apr 26. Acta Paediatr. 2022. PMID: 35416315
Black oesophagus in an adolescent with type 2 diabetes.
Quitadamo P, Caruso F, Bucci C, Del Monaco C, Verde A, Zanfardino A, Strisciuglio C, Piscopo A, Iafusco D, Mastrominico A, Caldore M. Quitadamo P, et al. Among authors: verde a. Lancet Diabetes Endocrinol. 2021 Sep;9(9):638. doi: 10.1016/S2213-8587(21)00187-X. Lancet Diabetes Endocrinol. 2021. PMID: 34416199 No abstract available.
Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: the experience in an Italian reference center.
Fecarotta S, Vaccaro L, Verde A, Alagia M, Rossi A, Colantuono C, Cacciapuoti MT, Annunziata P, Riccardo S, Grimaldi A, Fusco T, De Santis R, Barretta F, Albano L, Crisci D, Vallone F, Tarallo A, Cesana M, Brunetti-Pierri N, Frisso G, Ruoppolo M, Cacchiarelli D, Parenti G. Fecarotta S, et al. Among authors: verde a. Orphanet J Rare Dis. 2025 Jan 24;20(1):38. doi: 10.1186/s13023-025-03546-1. Orphanet J Rare Dis. 2025. PMID: 39856690
The Development and Initial Validation of the REST Questionnaire: A Multidimensional Tool for Assessing Fatigue in Individuals with and Without a History of Cancer.
Di Lorenzo G, Buonerba C, Baio R, Monteleone E, Passaro F, Tufano A, Montanaro V, Riccio V, Gallo I, Cappuccio F, Fortino F, Buonocore A, Monaco F, Verde A, Amato AR, Strianese O, Costabile F, Scafuri L. Di Lorenzo G, et al. Among authors: verde a. Diseases. 2025 Jan 15;13(1):15. doi: 10.3390/diseases13010015. Diseases. 2025. PMID: 39851479
Differences in technical and clinical perspectives on AI validation in cancer imaging: mind the gap!
Chouvarda I, Colantonio S, Verde ASC, Jimenez-Pastor A, Cerdá-Alberich L, Metz Y, Zacharias L, Nabhani-Gebara S, Bobowicz M, Tsakou G, Lekadir K, Tsiknakis M, Martí-Bonmati L, Papanikolaou N. Chouvarda I, et al. Among authors: verde asc. Eur Radiol Exp. 2025 Jan 15;9(1):7. doi: 10.1186/s41747-024-00543-0. Eur Radiol Exp. 2025. PMID: 39812924 Free PMC article.
207 results