Juan David Gonzalez Rodriguez

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Articles (21)

Collaborators (11)

Rebeca García Agudo

Head of Department

Katarzyna Taranta-Janusz

Assoc. Prof.

Medical University of Białystok

Albert C. M. Ong

University of Sheffield Medical School

UNITED KINGDOM

Milan Chromek

Karolinska Institutet

José Ramón Fernández‐Fructuoso

Maria Vanessa Perez-Gomez

Universidad Autónoma de Madrid

Joaquim Calado

Universidade de Aveiro

Elizabeth Córdoba-Lanús

Universidad de la Laguna

Dirk Schnabel

Charité - Universitätsmedizin Berlin

Bjoern Buchholz

Maria Szczepanska

Medical University of Silesia Faculty of Medical Sciences in Zabrze

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Juan David Gonzalez Rodriguez

Research Interests

Explore related searches

Contact this professor

Articles (21)

Collaborators (11)

Rebeca García Agudo

Katarzyna Taranta-Janusz

Albert C. M. Ong

Milan Chromek

José Ramón Fernández‐Fructuoso

Maria Vanessa Perez-Gomez

Joaquim Calado

Elizabeth Córdoba-Lanús

Dirk Schnabel

Bjoern Buchholz

Maria Szczepanska

Make your next move.

Juan David Gonzalez Rodriguez

Research Interests

Explore related searches

Contact this professor

Articles (21)

Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c.

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months

Update of the Spanish clinical practice guideline for urinary tract infection in infants and children. Summary of recommendations for diagnosis, treatment and follow-up

Actualización de la guía de práctica clínica española sobre infección del tracto urinario en la población pediátrica. Síntesis de las recomendaciones sobre diagnóstico, tratamiento y seguimiento

Role of dexamethasone in controlling the proinflammatory cytokine cascade in the first episode of paediatric acute pyelonephritis

Multidisciplinary management improves the genetic diagnosis of hereditary kidney diseases in the next generation sequencing (NGS) era

Sotos Syndrome and Nephrocalcinosis, a Rare But Possible Association due to Impact on Contiguous Genes.

β1-Integrin blockade prevents podocyte injury in experimental models of minimal change disease.

Reflections on TRP and TP/GFR in the definition of renal phosphate loss: conceptual review.

Mineral Metabolism in Children: Interrelation between Vitamin D and FGF23

Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases.

Pathogenic Variants of <i>SLC22A12</i> (URAT1) and <i>SLC2A9</i> (GLUT9) in Spanish Patients with Renal Hypouricemia: Founder Effect of <i>SLC2A9</i> Variant c.374C>T; p.(T125M)

Renal water handling in urinary tract infections

New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions

Transition of patients with metabolic bone disease from paediatric to adult healthcare services: current situation and proposals for improvement

Autosomal dominant polycystic kidney disease in young adults.

El manejo multidisciplinar mejora el diagnóstico genético de las enfermedades renales hereditarias en la era de next generation sequencing (NGS)

Dexamethasone to prevent kidney scarring in acute pyelonephritis: a randomized clinical trial

Peritoneal dialysis in the emergency management of severe neonatal hyperammonemia secondary to citrullinemia type 1.

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

Collaborators (11)

Rebeca García Agudo

Katarzyna Taranta-Janusz

Albert C. M. Ong

Milan Chromek

José Ramón Fernández‐Fructuoso

Maria Vanessa Perez-Gomez

Joaquim Calado

Elizabeth Córdoba-Lanús

Dirk Schnabel

Bjoern Buchholz

Maria Szczepanska

Make your next move.