Publications in collaboration with researchers from Complexo Hospitalario Universitario de Santiago (24)

2023

  1. Genetic testing in focal segmental glomerulosclerosis: in whom and when?

    Clinical Kidney Journal, Vol. 16, Núm. 11, pp. 2011-2022

2022

  1. Genetic Kidney Diseases (GKDs) Modeling Using Genome Editing Technologies

    Cells, Vol. 11, Núm. 9

  2. Quantitative Proteomic Study Unmasks Fibrinogen Pathway in Polycystic Liver Disease

    Biomedicines, Vol. 10, Núm. 2

2021

  1. Molecular basis, diagnostic challenges and therapeutic approaches of alport syndrome: A primer for clinicians

    International Journal of Molecular Sciences, Vol. 22, Núm. 20

  2. Molecular basis, diagnostic challenges and therapeutic approaches of bartter and gitelman syndromes: A primer for clinicians

    International Journal of Molecular Sciences, Vol. 22, Núm. 21

  3. Molecular pathophysiology of autosomal recessive polycystic kidney disease

    International Journal of Molecular Sciences, Vol. 22, Núm. 12

  4. Protein Extraction From FFPE Kidney Tissue Samples: A Review of the Literature and Characterization of Techniques

    Frontiers in Medicine, Vol. 8

  5. Tweak signaling pathway blockade slows cyst growth and disease progression in autosomal dominant polycystic kidney disease

    Journal of the American Society of Nephrology, Vol. 32, Núm. 8, pp. 1913-1932

2020

  1. CystAnalyser: A new software tool for the automatic detection and quantification of cysts in polycystic kidney and liver disease, and other cystic disorders

    PLoS Computational Biology, Vol. 16, Núm. 10

  2. First-Days Reduction of Plasma and Skin Advanced Glycation End Products is Related to Outcome in Septic Patients

    Shock, Vol. 53, Núm. 4, pp. 400-406

2019

  1. Dietary care for ADPKD patients: Current status and future directions

    Nutrients, Vol. 11, Núm. 7

2018

  1. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

    American Journal of Kidney Diseases, Vol. 72, Núm. 3, pp. 411-418

  2. Overview of autosomal dominant polycystic kidney disease in the south of Spain

    Nefrologia, Vol. 38, Núm. 2, pp. 220-221

2017

  1. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology

    Scientific Reports, Vol. 7, Núm. 1

  2. The genetic and cellular basis of autosomal dominant polycystic kidney disease-A primer for clinicians

    Frontiers in Pediatrics

2016

  1. A suppressor locus for MODY3-diabetes

    Scientific Reports, Vol. 6

  2. Autosomal recessive polycystic kidney disease diagnosed in a 39 year-old women with kidney failure and cramps

    Nefrologia

  3. The need for genetic study to diagnose some cases of distal renal tubular acidosis

    Nefrologia, Vol. 36, Núm. 5, pp. 552-555

2015

  1. Translational value of animal models of kidney failure

    European Journal of Pharmacology, Vol. 759, pp. 205-220

2014

  1. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1

    Journal of Molecular Medicine, Vol. 92, Núm. 10, pp. 1045-1056