Alejandro Garcia-Castaño

6PUBLICATIONS
33CO-AUTHORS
Cell and nuclear divisionPredictive and prognostic markersMedical biochemistry - inorganic elements and compoundsGene mapping
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Publications (6)

|Aug 10, 2026
Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

|Aug 08, 2025
Association of germline variants in the ZFX gene with primary hyperparathyroidism.

Ainhoa Camille Aranaga-Decori, Pedro González, Sara Gómez-Conde

|Sep 30, 2020
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia.

Alejandro García-Castaño, Leire Madariaga, Montserrat Antón-Gamero

|Sep 02, 2020
Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Alejandro García-Castaño, Ana Perdomo-Ramirez, Mònica Vall-Palomar

|Mar 14, 2017
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.

Alejandro García Castaño, Gustavo Pérez de Nanclares, Leire Madariaga

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Frequent Collaborators

4 joint publications

Leire Madariaga

3 joint publications

Gema Ariceta

1 joint publications

Ana Perdomo-Ramirez

1 joint publications

Mònica Vall-Palomar