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01/06/2025 CHALLENGES IN SYSTEMIC LUPUS ERYTHEMATOSUS IN SPANISH SPOCS SUB-COHORT OF MODERATE-SEVERE PATIENTS
Rúa-Figueroa, IJ, González, MF, Salman-Monte, TC, Segura, RC, Turrión, AI, Castellv, I, Alén, JC, Ajo, JB, Díaz, M, Ortego-Centeno, N, Rivas, NL, Cortés-Hernández, J, Alvarez-Hernández, P, Galvez-Fernandez, M, Bahamontes, N, Ding, B, Pego-Reigosa, JM. CHALLENGES IN SYSTEMIC LUPUS ERYTHEMATOSUS IN SPANISH SPOCS SUB-COHORT OF MODERATE-SEVERE PATIENTS. ANNALS OF THE RHEUMATIC DISEASES. 2025; 84DOI:10.1136/annrheumdis-2025-eular.B2398. PMID:. IF:20.600(Q1/1D).
01/06/2025 Diagnosis, management and treatment of the Alport syndrome-2024 guideline on behalf of ERKNet, ERA and ESPN
Torra, R, Lipska-Zietkiewicz, B, Acke, F, Antignac, C, Becker, JU, Gall, ECL, van Eerde, AM, Feltgen, N, Ferrari, R, Gale, DP, Gear, S, Gross, O, Hebaerle, S, Heidet, L, Lennon, R, Massella, L, Pfau, K, Pizarro, MDV, Topaloglu, R, Wlodkowski, T, Zealey, H. Diagnosis, management and treatment of the Alport syndrome-2024 guideline on behalf of ERKNet, ERA and ESPN. NEPHROLOGY DIALYSIS TRANSPLANTATION. 2025; 40(6)DOI:10.1093/ndt/gfae265. PMID:39673454. IF:5.600(Q1/1D).
01/05/2025 A predictive model of non-diabetic kidney disease in patients with diabetes mellitus and chronic kidney disease. A Spanish multi-center study
Bermejo, S, González, E, López-Revuelta, K, Ibernon, M, López, D, Martín-Gómez, A, Garcia-Osuna, R, Linares, T, Díaz, M, Martín, N, Barros, X, Marco, H, Navarro, MI, Esparza, N, Elias, S, Coloma, A, Robles, NR, Agraz, I, Poch, E, Rodas, L, Lozano, V, Fernández-Fernández, B, Hernández, E, Martínez, MI, Stanescu, RI, Moirón, JP, García-Fernández, N, Goicoechea, M, Calero, F, Bonet, J, Liaño, F, Pascual, J, Praga, M, Fulladosa, X, Soler, MJ. A predictive model of non-diabetic kidney disease in patients with diabetes mellitus and chronic kidney disease. A Spanish multi-center study. NEFROLOGIA. 2025; 45(5)DOI:10.1016/j.nefro.2024.12.007. PMID:40518653. IF:2.600(Q2/4D).
01/05/2025 Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working Group
Geertsema, P, Gansevoort, RT, Arici, M, Capasso, G, Gall, ECL, Furlano, M, Fuster, DG, Galletti, F, Dos Santos, VG, Gomez, MVP, Goumenos, D, Halbritter, J, Jambon, E, Korst, U, Leliveld-Kors, AM, Musquera, M, Figueiredo, A, Nijenhuis, T, Olsburgh, J, Pol, RA, Sayer, JA, Stippel, D, Torra, R, Müller, RU, Casteleijn, NF. Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working Group. NEPHROLOGY DIALYSIS TRANSPLANTATION. 2025; 40(5)DOI:10.1093/ndt/gfaf019. PMID:39848914. IF:5.600(Q1/1D).
01/05/2025 Inherited kidney disease and CAKUT are common causes of kidney failure requiring kidney replacement therapy: an ERA Registry study
Ortiz, A, Kramer, A, Ariceta, G, Arevalo, OLR, Gjerstad, AC, Santiuste, C, Trujillo-Aleman, S, Ferraro, PM, Methven, S, Santamaria, R, Naumovic, R, Resic, H, Hommel, K, Segelmark, M, Ambuehl, PM, Sorensen, SS, Parmentier, C, Vidal, E, Bakkaloglu, SA, Plumb, L, Palsson, R, Kerschbaum, J, ten Dam, MAGJ, Stel, VS, Jager, KJ, Torra, R. Inherited kidney disease and CAKUT are common causes of kidney failure requiring kidney replacement therapy: an ERA Registry study. NEPHROLOGY DIALYSIS TRANSPLANTATION. 2025; 40(5)DOI:10.1093/ndt/gfae240. PMID:39508350. IF:5.600(Q1/1D).
18/04/2025 Novel Truncating Variants in PODXL Represent a New Entity to Be Explored Among Podocytopathies
García-Aznar, JM, Besada-Cerecedo, ML, Castro-Alonso, C, Carpio, MS, Blasco, M, Quiroga, B, Cervienka, M, Mouzo, R, Torra, R, Ortiz, A, de Sequera, P. Novel Truncating Variants in PODXL Represent a New Entity to Be Explored Among Podocytopathies. Genes. 2025; 16(4)DOI:10.3390/genes16040464. PMID:40282423. IF:2.800(Q2/5D).