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Estimated GFR in autosomal dominant polycystic kidney disease: errors of an unpredictable method
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) causes about 10% of cases of end stage renal disease. Disease progression rate is heterogeneous. Tolvaptan is presently the only specific therapeutic option to slow kidney function decline in adults at risk of rapidly progressing ADPKD...
Autores principales: | Rodríguez, Rosa Miquel, Luis-Lima, Sergio, Fernandez, Juan Manuel, Gómez, María Vanesa Pérez, Toledo, Beatriz González, Cobo, Marian, Delgado-Mallén, Patricia, Escamilla, Beatriz, Marco, Cristina Oramas, Estupiñán, Sara, Perera, Coriolano Cruz, Mena, Natalia Negrín, Martín, Laura Díaz, Reyes, Sergio Pitti, González, Ibrahim Hernández, González-Rinne, Federico, González-Delgado, Alejandra, Ferrer-Moure, Carmen, Zulueta, Begoña López-Botet, Torres, Armando, Rodriguez Pérez, Jose Carlos, Gaspari, Flavio, Ortiz, Alberto, Porrini, Esteban |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584992/ https://www.ncbi.nlm.nih.gov/pubmed/35357684 http://dx.doi.org/10.1007/s40620-022-01286-0 |
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