Montserrat Anton-Gamero
Overview
Explore the profile of Montserrat Anton-Gamero including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
164
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0
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Recent Articles
1.
Azpilicueta-Idarreta M, Prieto-Torre M, Montijano-Herrero L, Fernandez-Ruiz L, Anton-Gamero M
An Pediatr (Engl Ed)
. 2023 Aug;
99(4):232-239.
PMID: 37598081
Introduction: Kidney injury associated with paediatric liver transplantation (LT) is common, but its evaluation is challenging. Our aim was to analyse the presence of perioperative acute kidney injury (AKI) and...
2.
Anton-Gamero M, Avila-Alvarez A, Balaguer-Martinez J, Bueno Campana M, Galera Martinez R
An Pediatr (Engl Ed)
. 2023 May;
98(6):401-408.
PMID: 37208201
No abstract available.
3.
Anton-Gamero M, Melgosa-Hijosa M
Clin Kidney J
. 2021 Oct;
14(10):2276-2277.
PMID: 34603708
No abstract available.
4.
Rodriguez-Rubio E, Gil-Pena H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernandez-Fernandez M, et al.
Orphanet J Rare Dis
. 2021 Apr;
16(1):154.
PMID: 33794951
No abstract available.
5.
Rodriguez-Rubio E, Gil-Pena H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernandez-Fernandez M, et al.
Orphanet J Rare Dis
. 2021 Feb;
16(1):104.
PMID: 33639975
Background: X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in PHEX gene leading tohypophosphatemia and high renal loss of phosphate. Rickets and growth retardation are the...
6.
Perdomo-Ramirez A, Anton-Gamero M, Rizzo D, Trindade A, Ramos-Trujillo E, Claverie-Martin F
Intractable Rare Dis Res
. 2020 Nov;
9(4):222-228.
PMID: 33139981
The oculocerebrorenal syndrome of Lowe is a rare X-linked disease characterized by congenital cataracts, proximal renal tubulopathy, muscular hypotonia and mental impairment. This disease is caused by mutations in the...
7.
Anton-Gamero M, de la Rosa I, Ortega Paez E
An Pediatr (Engl Ed)
. 2020 Nov;
94(1):62-63.
PMID: 33139205
No abstract available.
8.
Garcia-Castano A, Madariaga L, Anton-Gamero M, Mejia N, Ponce J, Gomez-Conde S, et al.
PLoS One
. 2020 Sep;
15(9):e0239965.
PMID: 32997713
The maintenance of magnesium (Mg2+) homeostasis is essential for human life. The Cystathionine-β-synthase (CBS)-pair domain divalent metal cation transport mediators (CNNMs) have been described to be involved in maintaining Mg2+...
9.
Hernandez-Frias O, Gil-Pena H, Perez-Roldan J, Gonzalez-Sanchez S, Ariceta G, Chocron S, et al.
Pediatr Nephrol
. 2019 Jan;
34(6):1077-1086.
PMID: 30607568
Objective: To find out if cardiovascular alterations are present in pediatric patients with X-linked hypophosphatemia (XLH). Study Design: Multicentre prospective clinical study on pediatric patients included in the RenalTube database...
10.
Rubio Cabezas O, Flanagan S, Stanescu H, Garcia-Martinez E, Caswell R, Lango-Allen H, et al.
J Am Soc Nephrol
. 2017 Apr;
28(8):2529-2539.
PMID: 28373276
Hyperinsulinemic hypoglycemia (HI) and congenital polycystic kidney disease (PKD) are rare, genetically heterogeneous disorders. The co-occurrence of these disorders (HIPKD) in 17 children from 11 unrelated families suggested an unrecognized...