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Year Number of Results
2004 1
2005 1
2006 1
2008 4
2010 3
2011 3
2012 1
2013 2
2015 1
2016 1
2017 2
2019 2
2020 3
2021 3
2022 2
2023 8
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2025 9

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48 results

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Page 1
Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency.
Kohn DB, Booth C, Shaw KL, Xu-Bayford J, Garabedian E, Trevisan V, Carbonaro-Sarracino DA, Soni K, Terrazas D, Snell K, Ikeda A, Leon-Rico D, Moore TB, Buckland KF, Shah AJ, Gilmour KC, De Oliveira S, Rivat C, Crooks GM, Izotova N, Tse J, Adams S, Shupien S, Ricketts H, Davila A, Uzowuru C, Icreverzi A, Barman P, Campo Fernandez B, Hollis RP, Coronel M, Yu A, Chun KM, Casas CE, Zhang R, Arduini S, Lynn F, Kudari M, Spezzi A, Zahn M, Heimke R, Labik I, Parrott R, Buckley RH, Reeves L, Cornetta K, Sokolic R, Hershfield M, Schmidt M, Candotti F, Malech HL, Thrasher AJ, Gaspar HB. Kohn DB, et al. Among authors: trevisan v. N Engl J Med. 2021 May 27;384(21):2002-2013. doi: 10.1056/NEJMoa2027675. Epub 2021 May 11. N Engl J Med. 2021. PMID: 33974366 Free PMC article. Clinical Trial.
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules.
Mastromoro G, Santoro C, Motta M, Sorrentino U, Daniele P, Peduto C, Petrizzelli F, Tripodi M, Pinna V, Zanobio M, Rotundo G, Bellacchio E, Lepri F, Farina A, D'Asdia MC, Piceci-Sparascio F, Biagini T, Petracca A, Castori M, Melis D, Accadia M, Traficante G, Tarani L, Fontana P, Sirchia F, Paparella R, Currò A, Benedicenti F, Scala I, Dentici ML, Leoni C, Trevisan V, Cecconi A, Giustini S, Pizzuti A, Salviati L, Novelli A, Zampino G, Zenker M, Genuardi M, Digilio MC, Papi L, Perrotta S, Nigro V, Castellanos E, Mazza T, Trevisson E, Tartaglia M, Piluso G, De Luca A. Mastromoro G, et al. Among authors: trevisan v. Genet Med. 2024 Nov;26(11):101241. doi: 10.1016/j.gim.2024.101241. Epub 2024 Aug 10. Genet Med. 2024. PMID: 39140257 Free article.
Relationship Between Loss of Y Chromosome and Urologic Cancers: New Future Perspectives.
Russo P, Bizzarri FP, Filomena GB, Marino F, Iacovelli R, Ciccarese C, Boccuto L, Ragonese M, Gavi F, Rossi F, Savoia C, Suraci PP, Falabella R, Pandolfo SD, Napolitano L, Leoni C, Trevisan V, Palermo G, Racioppi M, Sacco E, Muselaers S, Foschi N. Russo P, et al. Among authors: trevisan v. Cancers (Basel). 2024 Nov 8;16(22):3766. doi: 10.3390/cancers16223766. Cancers (Basel). 2024. PMID: 39594721 Free PMC article. Review.
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort.
Di Majo BE, Leoni C, Cartisano E, Fossati C, Viscogliosi G, Trevisan V, Bruno LP, Conti F, Moratti M, Monaco E, Rigante D, Rivalta B, Cancrini C, Szczawińska-Popłonyk A, Jamsheer A, Obara-Moszyńska M, Zakharova V, Shcherbina A, Rodina J, Tüysüz B, Jamuar SS, Lim JY, Goh J, Cereda A, Agovino T, Contaldo I, Gambardella ML, Balduzzi AC, Cherubino A, Marrocco GA, Bellesi S, Carusi V, Rumi G, Biondi A, Zampino G, Saettini F. Di Majo BE, et al. Among authors: trevisan v. Front Immunol. 2025 Jul 7;16:1598896. doi: 10.3389/fimmu.2025.1598896. eCollection 2025. Front Immunol. 2025. PMID: 40692796 Free PMC article.
A multi-step approach to overcome challenges in the management of head and neck lymphatic malformations, and response to treatment.
Trevisan V, De Corso E, Viscogliosi G, Onesimo R, Cina A, Panfili M, Perri L, Agazzi C, Giorgio V, Rigante D, Vento G, Papacci P, Paradiso FV, Silvaroli S, Nanni L, Resta N, Castori M, Galli J, Paludetti G, Zampino G, Leoni C. Trevisan V, et al. Orphanet J Rare Dis. 2024 Jul 23;19(1):276. doi: 10.1186/s13023-024-03200-2. Orphanet J Rare Dis. 2024. PMID: 39044220 Free PMC article.
Remestemcel-L for the treatment of graft versus host disease.
Locatelli F, Algeri M, Trevisan V, Bertaina A. Locatelli F, et al. Among authors: trevisan v. Expert Rev Clin Immunol. 2017 Jan;13(1):43-56. doi: 10.1080/1744666X.2016.1208086. Epub 2016 Jul 29. Expert Rev Clin Immunol. 2017. PMID: 27399600 Review.
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome.
Perri L, Viscogliosi G, Trevisan V, Brogna C, Chieffo DPR, Contaldo I, Alfieri P, Lentini N, Pastorino R, Zampino G, Leoni C. Perri L, et al. Among authors: trevisan v. Am J Med Genet B Neuropsychiatr Genet. 2025 Mar;198(2):e33009. doi: 10.1002/ajmg.b.33009. Epub 2024 Sep 27. Am J Med Genet B Neuropsychiatr Genet. 2025. PMID: 39333035
Clinical-Genetic Approach to Conditions with Macrocephaly and ASD/Behaviour Abnormalities: Variants in PTEN and PPP2R5D Are the Most Recurrent Gene Mutations in a Patient-Oriented Diagnostic Strategy.
L'Erario FF, Gazzellone A, Contaldo I, Veredice C, Carapelle M, Renzi AG, Modafferi C, Palucci M, D'Ambrosio P, Sonnini E, Loberti L, Panfili A, Lucci Cordisco E, Chiurazzi P, Trevisan V, Leoni C, Zampino G, Pomponi MG, Orteschi D, Zollino M, Marangi G. L'Erario FF, et al. Among authors: trevisan v. Genes (Basel). 2025 Apr 20;16(4):469. doi: 10.3390/genes16040469. Genes (Basel). 2025. PMID: 40282429 Free PMC article.
48 results