Leire Gondra

Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract

Leire Madariaga, Alejandro García‐Castaño, Gema Ariceta et al. · Clinical Kidney Journal · 2018 · 40 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutation

Leire Gondra, Stéphane Decramer, G. E. Chalouhi et al. · Pediatric Nephrology · 2016 · 23 citations

Medicine, Genetics, Molecular Genetics +13

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

Maartje F.A. Verploegen, Rosa Vargas‐Poussou, Stephen B. Walsh et al. · Nephrology Dialysis Transplantation · 2022 · 18 citations · Full text

Medicine, Endocrinology, Nephrology +17

Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis

Sara Gómez‐Conde, Alejandro García‐Castaño, Mireia Aguirre et al. · Pediatric Nephrology · 2021 · 17 citations

Medicine, Molecular Medicine, Nephrology +14

Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1

Cristina Martín-Higueras, Lodovica Borghese, Armando Torres et al. · Kidney International Reports · 2023 · 10 citations · Full text

Pharmacy, Nephrology, Pharmacotherapy +14