Leire Madariaga

ResearcherID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 14

Top Venues

Circulation. Genomic and precision medicine

Pediatric nephrology (Berlin, Germany)

Molecular genetics & genomic medicine

Nutrients

Universidad del País Vasco - Campus Bizkaia

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universidad del País Vasco - Campus Bizkaia

Spain

Associate professor :: Pediatrics

Biocruces Bizkaia Health Research Institute

Spain

Coordinator :: Rare inherited renal diseases

Hospital Universitario Cruces

Spain

Consultant :: Pediatric Neprology

Publications

Fernando De Frutos, Carles Diez-López, Elena García-Romero, Leire Gondra, Leire Madariaga, Gema Ariceta, Alejandro García Castaño, Edoardo Melilli, Lorena Herrador, Laura Triguero-Llonch, Ferran Gran, Laia Rosenfeld, Roger Llatjos, Josep Comin-Colet, José González-Costello
Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant. Circulation. Genomic and precision medicine 17 (2) (2024)
Fernando De Frutos, Carles Diez-López, Elena García-Romero, Leire Gondra, Leire Madariaga, Gema Ariceta, Alejandro García Castaño, Edoardo Melilli, Lorena Herrador, Laura Triguero-Llonch, Ferran Gran, Laia Rosenfeld, Roger Llatjos, Josep Comin-Colet, José González-Costello
Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant. Circulation. Genomic and precision medicine (2024)
Fernando De Frutos, Carles Diez-López, Elena García-Romero, Leire Gondra, Leire Madariaga, Gema Ariceta, Alejandro García Castaño, Edoardo Melilli, Lorena Herrador, Laura Triguero-Llonch, Ferran Gran, Laia Rosenfeld, Roger Llatjos, Josep Comin-Colet, José González-Costello
Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant. Circulation. Genomic and precision medicine 17 (2) (2024)
Fernando De Frutos, Carles Diez-López, Elena García-Romero, Leire Gondra, Leire Madariaga, Gema Ariceta, Alejandro García Castaño, Edoardo Melilli, Lorena Herrador, Laura Triguero-Llonch, Ferran Gran, Laia Rosenfeld, Roger Llatjos, Josep Comin-Colet, José González-Costello
Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant. Circulation. Genomic and precision medicine 17 (2) (2024)
Alejandro García-Castaño, Sara Gómez-Conde, Leire Gondra, María Herrero, Mireia Aguirre, Ana-Belén de la Hoz, Luis Castaño, null null, Leire Madariaga
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3. Scientific reports 13 (1) (2023)
María Herrero-Goñi, Amaia Zugazabeitia Irazábal, Leire Madariaga, Estibaliz Chávarri Gil, Leire Gondra, Mireia Aguirre Meñica
Use of rasburicase to improve kidney function in children with hyperuricemia and acute kidney injury. Clinical and experimental nephrology (2023)
Luis Castano, Leire Madariaga, Gema Grau, Alejandro García-Castaño
25(OH)Vitamin D Deficiency and Calcifediol Treatment in Pediatrics. Nutrients 14 (9) (2022)
Mònica Vall-Palomar, Leire Madariaga, Gema Ariceta
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Pediatric nephrology (Berlin, Germany) 36 (10) (2021)
Andrea Domingo-Gallego, Marc Pybus, Leire Madariaga, Juan Alberto Piñero-Fernández, Sara González-Pastor, Mercedes López-González, Esther Simarro-Rueda, María Luisa Quintanilla-Mata, María Luisa Matoses-Ruipérez, Laia Ejarque-Vila, Emilie Cornec-Le Gall, Lluís Guirado, Roser Torra, Gema Ariceta, Elisabet Ars
Clinical and genetic characterization of a cohort of proteinuric patients with biallelic CUBN variants. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association (2021)
Sara Gómez-Conde, Alejandro García-Castaño, Mireia Aguirre, María Herrero, Leire Gondra, Nélida García-Pérez, Paula García-Ledesma, Luis Martín-Penagos, Cecilia Dall'Anese, Gema Ariceta, Luis Castaño, Leire Madariaga
Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis. Pediatric nephrology (Berlin, Germany) 36 (10) (2021)
Alejandro García Castaño, Ana Perdomo-Ramírez, Mònica Vall-Palomar, Elena Ramos-Trujillo, Leire Madariaga, Gema Ariceta, Felix Claverie-Martin
Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Molecular genetics & genomic medicine 8 (11) (2020)
Francisco de la Cerda-Ojeda, Juan David González-Rodríguez, Leire Madariaga, Guillermo Martínez-Díaz-Guerra, María L Matoses-Ruipérez
Hypophosphataemic Rickets: Similar Phenotype of Different Diseases. Advances in therapy 37 (Suppl 2) (2020)
Alejandro García Castaño, Leire Madariaga, Montserrat Antón-Gamero, Natalia Mejia, Jenny Ponce, Sara Gómez-Conde, Gustavo Pérez de Nanclares, Ana Belén De la Hoz, Rosa Martínez, Laura Saso, Idoia Martínez de LaPiscina, Inés Urrutia, Olaia Velasco, Aníbal Aguayo, Luis Castaño, Sonia Gaztambide
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia. PloS one 15 (9) (2020)
Leire Madariaga, Alejandro García-Castaño, Gema Ariceta, Rosa Martínez-Salazar, Aníbal Aguayo, Luis Castaño, null null
Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract. Clinical kidney journal 12 (3) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Leire Madariaga