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Year | Number of Results |
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2022 | 2 |
2023 | 2 |
2024 | 0 |
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Page 1
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes.
Cells. 2022 Dec 16;11(24):4096. doi: 10.3390/cells11244096.
Cells. 2022.
PMID: 36552859
Free PMC article.
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.
Bergantini L, Baldassarri M, d'Alessandro M, Brunelli G, Fabbri G, Zguro K, Degl'Innocenti A; GEN-COVID Multicenter study; Fallerini C, Bargagli E, Renieri A.
Bergantini L, et al.
Respir Res. 2023 Jun 16;24(1):158. doi: 10.1186/s12931-023-02458-7.
Respir Res. 2023.
PMID: 37328761
Free PMC article.
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Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy.
Serio VB, Palmieri M, Loberti L, Granata S, Fallerini C, Vaghi M, Renieri A, Pinto AM.
Serio VB, et al.
J Clin Med. 2022 Jun 28;11(13):3740. doi: 10.3390/jcm11133740.
J Clin Med. 2022.
PMID: 35807022
Free PMC article.
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Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors.
Serio VB, Palmieri M, Innamorato S, Loberti L, Fallerini C, Ariani F, Antolini E, Covarelli J, Vaghi M, Frullanti E, Renieri A, Pinto AM.
Serio VB, et al.
Front Genet. 2023 Aug 17;14:1213283. doi: 10.3389/fgene.2023.1213283. eCollection 2023.
Front Genet. 2023.
PMID: 37662840
Free PMC article.
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