Showing results (141-150 of 161) with videos related to
Sort By:
Pageof 17
EJNMMI Reports|April 23, 2025
Brazilian profile of Radium-223 in metastatic prostate cancer: a multicentric, retrospective studyStephan Souza, Felipe Ribeiro, Ana Brito, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 2025
Predicting mortality and short-term outcomes of continuous kidney replacement therapies in neonates and infantsAnna Deja, Kamil Deja, Andrea Cappoli, et al.Kidney International|January 10, 2014
Genotype-phenotype associations in WT1 glomerulopathyBeata S Lipska, Bruno Ranchin, Paraskevas Iatropoulos, et al.Journal of Nephrology|April 6, 2019
Acute dialysis in children: results of a European surveyIsabella Guzzo, Lara de Galasso, Sevgi Mir, et al.The Journal of Pathology|October 29, 2025
MicroRNA profiling of testicular Leydig cell tumors identifies a microRNA signature associated with malignancy and miR-196b-5p as a potentially useful biomarkerJoão Lobo, Nuno Tiago Tavares, Fernanda Fernandes-Pontes, et al.Allergy|November 16, 2024
Efficacy and safety of intranasal medications for allergic rhinitis: Network meta-analysisBernardo Sousa-Pinto, Rafael José Vieira, Antonio Bognanni, et al.Nature Genetics|October 16, 2007
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer riskPeter Broderick, Luis Carvajal-Carmona, Alan M Pittman, et al.Acta Reumatologica Portuguesa|November 11, 2006
[Tuberculosis in rheumatic patients treated with tumour necrosis factor alpha antagonists: the Portuguese experience]João Eurico Fonseca, Helena Canhão, Cândida Silva, et al.Clinical Journal of the American Society of Nephrology : CJASN|April 21, 2018
Prevalence of Hypertension in Children with Early-Stage ADPKDLaura Massella, Djalila Mekahli, Dušan Paripović, et al.Kidney International|May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKathrin Burgmaier, Leonie Brinker, Florian Erger, et al.Pageof 17