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Renal tubular acidosis.
Gil-Peña H, Mejía N, Santos F. Gil-Peña H, et al. Among authors: mejia n. J Pediatr. 2014 Apr;164(4):691-698.e1. doi: 10.1016/j.jpeds.2013.10.085. Epub 2013 Dec 15. J Pediatr. 2014. PMID: 24345454 No abstract available.
Longitudinal growth in chronic hypokalemic disorders.
Gil-Peña H, Mejia N, Alvarez-Garcia O, Loredo V, Santos F. Gil-Peña H, et al. Among authors: mejia n. Pediatr Nephrol. 2010 Apr;25(4):733-7. doi: 10.1007/s00467-009-1330-7. Epub 2009 Nov 10. Pediatr Nephrol. 2010. PMID: 19902272 Review.
Hypophosphatemia and growth.
Santos F, Fuente R, Mejia N, Mantecon L, Gil-Peña H, Ordoñez FA. Santos F, et al. Among authors: mejia n. Pediatr Nephrol. 2013 Apr;28(4):595-603. doi: 10.1007/s00467-012-2364-9. Epub 2012 Nov 22. Pediatr Nephrol. 2013. PMID: 23179196 Review.
Growth of kidney-transplanted pediatric patients treated with sirolimus.
González D, García CD, Azócar M, Waller S, Alonso A, Ariceta G, Mejía N, Santos F. González D, et al. Among authors: mejia n. Pediatr Nephrol. 2011 Jun;26(6):961-6. doi: 10.1007/s00467-011-1811-3. Epub 2011 Mar 5. Pediatr Nephrol. 2011. PMID: 21380626
Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm.
García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Madrid A, Nadal I, Navarro M, Lucas E, Fijo J, Espino M, Espitaletta Z, Castaño L, Ariceta G; RenalTube Group. García Castaño A, et al. PLoS One. 2013 Sep 18;8(9):e74673. doi: 10.1371/journal.pone.0074673. eCollection 2013. PLoS One. 2013. PMID: 24058621 Free PMC article.
Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Claverie-Martín F, García-Nieto V, Loris C, Ariceta G, Nadal I, Espinosa L, Fernández-Maseda Á, Antón-Gamero M, Avila A, Madrid Á, González-Acosta H, Córdoba-Lanus E, Santos F, Gil-Calvo M, Espino M, García-Martinez E, Sanchez A, Muley R; RenalTube Group. Claverie-Martín F, et al. PLoS One. 2013;8(1):e53151. doi: 10.1371/journal.pone.0053151. Epub 2013 Jan 3. PLoS One. 2013. PMID: 23301036 Free PMC article.
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia.
García-Castaño A, Madariaga L, Antón-Gamero M, Mejia N, Ponce J, Gómez-Conde S, Pérez de Nanclares G, De la Hoz AB, Martínez R, Saso L, Martínez de LaPiscina I, Urrutia I, Velasco O, Aguayo A, Castaño L, Gaztambide S. García-Castaño A, et al. Among authors: mejia n. PLoS One. 2020 Sep 30;15(9):e0239965. doi: 10.1371/journal.pone.0239965. eCollection 2020. PLoS One. 2020. PMID: 32997713 Free PMC article.
110 results