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01/07/2021
Intracavernous Branches of the Internal Carotid Artery Through an Endoscopic Endonasal Approach: Anatomical Study and Review of the Literature
Aibar-Duran, JA, Munoz-Hernandez, F, Asencio-Cortes, C, Montserrat-Gili, J, Gras-Cabrerizo, JR, Mirapeix, RM. Intracavernous Branches of the Internal Carotid Artery Through an Endoscopic Endonasal Approach: Anatomical Study and Review of the Literature. World Neurosurgery. 2021; 151DOI:10.1016/j.wneu.2021.04.046. PMID:33887498. IF:2.210(Q3/6D).
01/01/2022
Guidelines for Genetic Testing and Management of Alport Syndrome
Savige, J, Lipska-Zietkiewicz, BS, Watson, E, Hertz, JM, Deltas, C, Mari, F, Hilbert, P, Plevova, P, Byers, P, Cerkauskaite, A, Gregory, M, Cerkauskiene, R, Ljubanovic, DG, Becherucci, F, Errichiello, C, Massella, L, Aiello, V, Lennon, R, Hopkinson, L, Koziell, A, Lungu, A, Rothe, HM, Hoefele, J, Zacchia, M, Martic, TN, Gupta, A, van Eerde, A, Gear, S, Landini, S, Palazzo, V, al-Rabadi, L, Claes, K, Corveleyn, A, Van Hoof, E, van Geel, M, Williams, M, Ashton, E, Belge, H, Ars, E, Bierzynska, A, Gangemi, C, Renieri, A, Storey, H, Flinter, F. Guidelines for Genetic Testing and Management of Alport Syndrome. Clinical Journal of the American Society of Nephrology. 2022; 17(1)DOI:10.2215/CJN.04230321. PMID:34930753. IF:9.800(Q1/1D).
01/12/2021
Deciphering transplant outcomes of expanded kidney allografts donated after controlled circulatory death in the current transplant era. A call for caution
Montero, N, Toapanta, N, Pallares, N, Crespo, M, Diekmann, F, Guirado, L, Esteban, R, Codina, S, Melilli, E, Buxeda, A, Velis, G, Torres, IB, Revuelta, I, Andujar, AM, Facundo, C, Bardaji, B, Riera, L, Fiol, M, Cruzado, JM, Comas, J, Giral, M, Naesens, M, Asberg, A, Moreso, F, Bestard, O. Deciphering transplant outcomes of expanded kidney allografts donated after controlled circulatory death in the current transplant era. A call for caution. TRANSPLANT INTERNATIONAL. 2021; 34(12)DOI:10.1111/tri.14131. PMID:34626501. IF:3.842(Q1/3D).
01/11/2021
Autosomal dominant polycystic kidney disease: possibly the least silent cause of chronic kidney disease
Torra, R, Perez-Gomez, MV, Furlano, M. Autosomal dominant polycystic kidney disease: possibly the least silent cause of chronic kidney disease. Clinical Kidney Journal. 2021; 14(11)DOI:10.1093/ckj/sfab132. PMID:34754424. IF:5.860(Q1/2D).