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Stem Cell Reports|March 11, 2015
Direct reprogramming of human bone marrow stromal cells into functional renal cells using cell-free extractsEvangelia Papadimou, Marina Morigi, Paraskevas Iatropoulos, et al.Journal of the American Society of Nephrology : JASN|October 15, 2017
Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GNParaskevas Iatropoulos, Erica Daina, Manuela Curreri, et al.Molecular Immunology|February 20, 2016
Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcomeParaskevas Iatropoulos, Marina Noris, Caterina Mele, et al.Clinical Journal of the American Society of Nephrology : CJASN|April 10, 2015
Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic SyndromeCaterina Mele, Mathieu Lemaire, Paraskevas Iatropoulos, et al.Italian Journal of Pediatrics|September 15, 2020
Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases networkMarco Salvatore, Agata Polizzi, Maria Chiara De Stefano, et al.The New England Journal of Medicine|July 16, 2011
MYO1E mutations and childhood familial focal segmental glomerulosclerosisCaterina Mele, Paraskevas Iatropoulos, Roberta Donadelli, et al.Kidney International|January 10, 2014
Genotype-phenotype associations in WT1 glomerulopathyBeata S Lipska, Bruno Ranchin, Paraskevas Iatropoulos, et al.Kidney International|March 22, 2013
Genetic screening in adolescents with steroid-resistant nephrotic syndromeBeata S Lipska, Paraskevas Iatropoulos, Ramona Maranta, et al.Pageof 2