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Page 1
No evidence of Fabry disease in a patient with the new p.Met70Val GLA gene variant.
Capelli I, Di Costanzo R, Aiello V, Lerario S, De Giovanni P, Montevecchi M, Cerretani D, Donadio V, La Manna G, Mignani R. Capelli I, et al. Among authors: lerario s. Mol Genet Genomic Med. 2024 Jun;12(6):e2390. doi: 10.1002/mgg3.2390. Mol Genet Genomic Med. 2024. PMID: 38895855 Free PMC article.
Fabry disease: a rare disorder calling for personalized medicine.
Lerario S, Monti L, Ambrosetti I, Luglio A, Pietra A, Aiello V, Montanari F, Bellasi A, Zaza G, Galante A, Salera D, Capelli I, La Manna G, Provenzano M. Lerario S, et al. Int Urol Nephrol. 2024 Oct;56(10):3161-3172. doi: 10.1007/s11255-024-04042-4. Epub 2024 Apr 13. Int Urol Nephrol. 2024. PMID: 38613662 Free PMC article. Review.
DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort.
Aiello V, Ciurli F, Conti A, Cristalli CP, Lerario S, Montanari F, Sciascia N, Vischini G, Fabbrizio B, Di Costanzo R, Olivucci G, Pietra A, Lopez A, Zambianchi L, La Manna G, Capelli I. Aiello V, et al. Among authors: lerario s. Genes (Basel). 2023 Dec 19;15(1):3. doi: 10.3390/genes15010003. Genes (Basel). 2023. PMID: 38275584 Free PMC article.
Empagliflozin in Patients with Chronic Kidney Disease.
The EMPA-KIDNEY Collaborative Group; Herrington WG, Staplin N, Wanner C, Green JB, Hauske SJ, Emberson JR, Preiss D, Judge P, Mayne KJ, Ng SYA, Sammons E, Zhu D, Hill M, Stevens W, Wallendszus K, Brenner S, Cheung AK, Liu ZH, Li J, Hooi LS, Liu W, Kadowaki T, Nangaku M, Levin A, Cherney D, Maggioni AP, Pontremoli R, Deo R, Goto S, Rossello X, Tuttle KR, Steubl D, Petrini M, Massey D, Eilbracht J, Brueckmann M, Landray MJ, Baigent C, Haynes R. The EMPA-KIDNEY Collaborative Group, et al. N Engl J Med. 2023 Jan 12;388(2):117-127. doi: 10.1056/NEJMoa2204233. Epub 2022 Nov 4. N Engl J Med. 2023. PMID: 36331190 Free PMC article. Clinical Trial.
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