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Vestibular and audiological findings in the Alport syndrome.
Barozzi S, Soi D, Intieri E, Giani M, Aldè M, Tonon E, Signorini L, Renieri A, Fallerini C, Perin P, Montini G, Ambrosetti U. Barozzi S, et al. Among authors: montini g. Am J Med Genet A. 2020 Oct;182(10):2345-2358. doi: 10.1002/ajmg.a.61796. Epub 2020 Aug 20. Am J Med Genet A. 2020. PMID: 32820599
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases.
Mastrangelo A, Giani M, Groppali E, Castorina P, Soldà G, Robusto M, Fallerini C, Bruttini M, Renieri A, Montini G. Mastrangelo A, et al. Among authors: montini g. Front Med (Lausanne). 2020 Nov 23;7:580376. doi: 10.3389/fmed.2020.580376. eCollection 2020. Front Med (Lausanne). 2020. PMID: 33330536 Free PMC article.
Born with a solitary kidney: at risk of hypertension.
La Scola C, Marra G, Ammenti A, Pasini A, Taroni F, Bertulli C, Morello W, Ceccoli M, Mencarelli F, Guarino S, Puccio G, Montini G. La Scola C, et al. Among authors: montini g. Pediatr Nephrol. 2020 Aug;35(8):1483-1490. doi: 10.1007/s00467-020-04535-1. Epub 2020 Mar 24. Pediatr Nephrol. 2020. PMID: 32211991 Free PMC article.
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion.
Marasca F, Sinha S, Vadalà R, Polimeni B, Ranzani V, Paraboschi EM, Burattin FV, Ghilotti M, Crosti M, Negri ML, Campagnoli S, Notarbartolo S, Sartore-Bianchi A, Siena S, Prati D, Montini G, Viale G, Torre O, Harari S, Grifantini R, Soldà G, Biffo S, Abrignani S, Bodega B. Marasca F, et al. Among authors: montini g. Nat Genet. 2022 Feb;54(2):180-193. doi: 10.1038/s41588-021-00989-7. Epub 2022 Jan 17. Nat Genet. 2022. PMID: 35039641
333 results