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Nutrients|May 14, 2022
25(OH)Vitamin D Deficiency and Calcifediol Treatment in PediatricsLuis Castano, Leire Madariaga, Gema Grau, et al.
European Journal of Endocrinology|November 9, 2018
Novel mutations associated with inherited human calcium-sensing receptor disorders: A clinical genetic studyAlejandro García-Castaño, Leire Madariaga, Gustavo Pérez de Nanclares, et al.
Nefrologia|September 27, 2022
Hereditary distal renal tubular acidosis: Genotypic correlation, evolution to long term, and new therapeutic perspectivesSara Gómez-Conde, Alejandro García-Castaño, Mireia Aguirre, et al.
Plos One|August 8, 2025
Association of germline variants in the ZFX gene with primary hyperparathyroidismAinhoa Camille Aranaga-Decori, Pedro González, Sara Gómez-Conde, et al.
Molecular Genetics & Genomic Medicine|September 2, 2020
Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosisAlejandro García-Castaño, Ana Perdomo-Ramirez, Mònica Vall-Palomar, et al.
Scientific Reports|August 3, 2023
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3Alejandro García-Castaño, Sara Gómez-Conde, Leire Gondra, et al.
Endocrinology, Diabetes & Metabolism Case Reports|December 12, 2018
Identification of a novel large CASR deletion in a patient with familial hypocalciuric hypercalcemiaAlejandro García-Castaño, Leire Madariaga, Sharona Azriel, et al.
Pediatric Nephrology (Berlin, Germany)|April 21, 2021
Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosisSara Gómez-Conde, Alejandro García-Castaño, Mireia Aguirre, et al.
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