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Page 1
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: martinez v. 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.
Spanish guidelines for the management of autosomal dominant polycystic kidney disease.
Ars E, Bernis C, Fraga G, Martínez V, Martins J, Ortiz A, Rodríguez-Pérez JC, Sans L, Torra R; Spanish Working Group on Inherited Kidney Disease. Ars E, et al. Among authors: martinez v. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4:iv95-105. doi: 10.1093/ndt/gfu186. Nephrol Dial Transplant. 2014. PMID: 25165191
Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1.
Ayasreh N, Bullich G, Miquel R, Furlano M, Ruiz P, Lorente L, Valero O, García-González MA, Arhda N, Garin I, Martínez V, Pérez-Gómez V, Fulladosa X, Arroyo D, Martínez-Vea A, Espinosa M, Ballarín J, Ars E, Torra R. Ayasreh N, et al. Among authors: martinez v, martinez vea a. Am J Kidney Dis. 2018 Sep;72(3):411-418. doi: 10.1053/j.ajkd.2018.03.019. Epub 2018 May 18. Am J Kidney Dis. 2018. PMID: 29784615
Recommendations for the management of renal involvement in the tuberous sclerosis complex.
Ariceta G, Buj MJ, Furlano M, Martínez V, Matamala A, Morales M, Robles NR, Sans L, Villacampa F, Torra R. Ariceta G, et al. Among authors: martinez v. Nefrologia (Engl Ed). 2020 Mar-Apr;40(2):142-151. doi: 10.1016/j.nefro.2019.07.002. Epub 2019 Nov 10. Nefrologia (Engl Ed). 2020. PMID: 31722796 Free article. English, Spanish.
Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Diseases. Review 2020.
Ars E, Bernis C, Fraga G, Furlano M, Martínez V, Martins J, Ortiz A, Pérez-Gómez MV, Rodríguez-Pérez JC, Sans L, Torra R; en nombre del grupo de trabajo de Enfermedades Renales Hereditarias de la Sociedad Española de Nefrología. Ars E, et al. Among authors: martinez v. Nefrologia (Engl Ed). 2022 Jul-Aug;42(4):367-389. doi: 10.1016/j.nefroe.2022.11.011. Epub 2022 Nov 17. Nefrologia (Engl Ed). 2022. PMID: 36404270 Free article.
Autosomal dominant polycystic kidney disease in young adults.
Martínez V, Furlano M, Sans L, Pulido L, García R, Pérez-Gómez MV, Sánchez-Rodríguez J, Blasco M, Castro-Alonso C, Fernández-Fresnedo G, Robles NR, Valenzuela MP, Naranjo J, Martín N, Pilco M, Agraz-Pamplona I, González-Rodríguez JD, Panizo N, Fraga G, Fernández L, López MT, Dall'Anese C, Ortiz A, Torra R; participants in the REPQRAD. Martínez V, et al. Clin Kidney J. 2022 Nov 29;16(6):985-995. doi: 10.1093/ckj/sfac251. eCollection 2023 Jun. Clin Kidney J. 2022. PMID: 37260991 Free PMC article.
Increased prevalence of kidney cysts in individuals carrying heterozygous COL4A3 or COL4A4 pathogenic variants.
Furlano M, Pilco-Teran M, Pybus M, Martínez V, Aza-Carmona M, Rius Peris A, Pérez-Gomez V, Berná G, Mazon J, Hernández J, Fayos de Arizón L, Viera E, Gich I, Pérez HV, Gomá-Garcés E, Albero Dolon JL, Ars E, Torra R. Furlano M, et al. Among authors: martinez v. Nephrol Dial Transplant. 2024 Aug 30;39(9):1442-1448. doi: 10.1093/ndt/gfae031. Nephrol Dial Transplant. 2024. PMID: 38317457 Free PMC article.
Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.
Pena-Couso L, Ercibengoa M, Mercadillo F, Gómez-Sánchez D, Inglada-Pérez L, Santos M, Lanillos J, Gutiérrez-Abad D, Hernández A, Carbonell P, Letón R, Robledo M, Rodríguez-Antona C, Perea J, Urioste M; PHTS Working Group. Pena-Couso L, et al. Orphanet J Rare Dis. 2022 Feb 28;17(1):85. doi: 10.1186/s13023-021-02079-7. Orphanet J Rare Dis. 2022. PMID: 35227301 Free PMC article.
1,459 results