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Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype.
Am J Hum Genet. 2022 Jan 6;109(1):136-156. doi: 10.1016/j.ajhg.2021.11.016. Epub 2021 Dec 9.
Am J Hum Genet. 2022.
PMID: 34890546
Free PMC article.
Tolvaptan-induced remission of primary palmar hyperhidrosis in a patient with ADPKD: a serendipitous finding.
Cuka E, Vespa M, Joli G, Manunta P, Sciarrone Alibrandi TM.
Cuka E, et al. Among authors: joli g.
J Nephrol. 2022 Mar;35(2):671-674. doi: 10.1007/s40620-021-00973-8. Epub 2021 Feb 8.
J Nephrol. 2022.
PMID: 33555573
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[Covid-19 vaccination and renal patients: overcoming unwarranted fears and re-establishing priorities].
Sciarrone Alibrandi MT, Vespa M, Joli G, Bucci R, Brioni E, Rivera RF.
Sciarrone Alibrandi MT, et al. Among authors: joli g.
G Ital Nefrol. 2021 Apr 14;38(2):2021-vol2.
G Ital Nefrol. 2021.
PMID: 33852219
Italian.
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[The Management of Patients with Adult Autosomal Dominant Polycystic Kidney Disease (ADPKD) Requires a Multidisciplinary Approach].
Bucci R, De Rosa LI, Brambilla Pisoni M, Farinone S, Vespa M, Joli G, Catania M, Kola K, Tunesi F, Brioni E, Carrera P, Mancassola G, Citterio L, Manunta P, Vezzoli G, Sciarrone Alibrandi MT.
Bucci R, et al. Among authors: joli g.
G Ital Nefrol. 2023 Dec 22;40(6):2023-vol6.
G Ital Nefrol. 2023.
PMID: 38156543
Italian.
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