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Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study.
Furlano M, Martínez V, Pybus M, Arce Y, Crespí J, Venegas MDP, Bullich G, Domingo A, Ayasreh N, Benito S, Lorente L, Ruíz P, Gonzalez VL, Arlandis R, Cabello E, Torres F, Guirado L, Ars E, Torra R. Furlano M, et al. Among authors: crespi j. Am J Kidney Dis. 2021 Oct;78(4):560-570.e1. doi: 10.1053/j.ajkd.2021.02.326. Epub 2021 Apr 7. Am J Kidney Dis. 2021. PMID: 33838161 Free article.
MYH9 Associated nephropathy.
Furlano M, Arlandis R, Venegas MDP, Novelli S, Crespi J, Bullich G, Ayasreh N, Remacha Á, Ruiz P, Lorente L, Ballarín J, Matamala A, Ars E, Torra R. Furlano M, et al. Among authors: crespi j. Nefrologia (Engl Ed). 2019 Mar-Apr;39(2):133-140. doi: 10.1016/j.nefro.2018.08.008. Epub 2018 Nov 22. Nefrologia (Engl Ed). 2019. PMID: 30471777 Free article. Review. English, Spanish.
The Benefits of Early versus Late Therapeutic Intervention in Fabry Disease.
Furlano M, Ars E, Matamala A, Brossa V, Martí J, Del Prado-Venegas M, Crespi J, Roe E, Torra R. Furlano M, et al. Among authors: crespi j. Case Rep Genet. 2022 Dec 30;2022:3208810. doi: 10.1155/2022/3208810. eCollection 2022. Case Rep Genet. 2022. PMID: 36619006 Free PMC article.
Combined retinal detachment and candida chorioretinitis.
Vela JI, Roselló N, Díaz-Cascajosa J, Crespí J, Buil JA. Vela JI, et al. Among authors: crespi j. BMJ Case Rep. 2010 Nov 5;2010:bcr0120102648. doi: 10.1136/bcr.01.2010.2648. BMJ Case Rep. 2010. PMID: 22791844 Free PMC article.
38 results