Alejandro Castano-Garcia
Barakaldo, PV, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 27 publications
Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).
Journal: Kidney360
Published: January 15, 2026
Concordant epigenetic and discordant clinical PHP1B/iPPSD3 manifestations in two monozygotic adolescent twins.
Journal: Clinical epigenetics
Published: October 29, 2025
Correction: Genetic profile of a large Spanish cohort with hypercalcemia.
Journal: Frontiers in endocrinology
Published: October 23, 2025
Association of germline variants in the ZFX gene with primary hyperparathyroidism.
Journal: PloS one
Published: April 26, 2025
Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic Perspectives.
Journal: Kidney international reports
Published: February 03, 2025
Dilated Cardiomyopathy With Concomitant Salt-Losing Renal Tubulopathy Caused by Heterozygous RRAGD Gene Variant.
Journal: Circulation. Genomic and precision medicine
Published: February 19, 2024
Genetic profile of a large Spanish cohort with hypercalcemia.
Journal: Frontiers in endocrinology
Published: September 20, 2023
Hypercalcemia in patients with mutations in NR3C2 and SCNN1B
Journal: Medicina clinica
Published: May 30, 2023
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3.
Journal: Scientific reports
Published: January 13, 2023
25(OH)Vitamin D Deficiency and Calcifediol Treatment in Pediatrics.
Journal: Nutrients
Published: March 30, 2022
Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 06, 2020
Five patients with disorders of calcium metabolism presented with GCM2 gene variants.
Journal: Scientific reports
Published: September 09, 2020
Last Updated: 09/26/2026