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Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
Rodríguez-Rubio E, Gil-Peña H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernández-Fernández M, de Lucas-Collantes C, Gil M, Luis-Yanes MI, Vergara I, González-Rodríguez JD, Ferrando S, Antón-Gamero M, Hidalgo-Barquero MC, Fernández-Escribano A, Fernández-Maseda MÁ, Espinosa L, Oliet A, Vicente A, Ariceta G, Santos F; RenalTubeGroup. Rodríguez-Rubio E, et al. Among authors: madariaga l. Orphanet J Rare Dis. 2021 Apr 1;16(1):154. doi: 10.1186/s13023-021-01786-5. Orphanet J Rare Dis. 2021. PMID: 33794951 Free PMC article. No abstract available.
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 mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study.
García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Chocron S, Madrid A, Lafita Tejedor FJ, Gil Campos M, Sánchez Del Pozo J, Ruiz Cano R, Espino M, Gomez Vida JM, Santos F, García Nieto VM, Loza R, Rodríguez LM, Hidalgo Barquero E, Printza N, Camacho JA, Castaño L, Ariceta G; RenalTube Group. García Castaño A, et al. Among authors: madariaga l. Eur J Pediatr. 2015 Oct;174(10):1373-85. doi: 10.1007/s00431-015-2534-4. Epub 2015 Apr 23. Eur J Pediatr. 2015. PMID: 25902753
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.
García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Madrid Á, Chocrón S, Nadal I, Navarro M, Lucas E, Fijo J, Espino M, Espitaletta Z, García Nieto V, Barajas de Frutos D, Loza R, Pintos G, Castaño L; RenalTube Group; Ariceta G. García Castaño A, et al. Among authors: madariaga l. PLoS One. 2017 Mar 13;12(3):e0173581. doi: 10.1371/journal.pone.0173581. eCollection 2017. PLoS One. 2017. PMID: 28288174 Free PMC article.
Risk of cardiovascular involvement in pediatric patients with X-linked hypophosphatemia.
Hernández-Frías O, Gil-Peña H, Pérez-Roldán JM, González-Sanchez S, Ariceta G, Chocrón S, Loza R, de la Cerda Ojeda F, Madariaga L, Vergara I, Fernández-Fernández M, Ferrando-Monleón S, Antón-Gamero M, Fernández-Maseda Á, Luis-Yanes MI, Santos F. Hernández-Frías O, et al. Among authors: madariaga l. Pediatr Nephrol. 2019 Jun;34(6):1077-1086. doi: 10.1007/s00467-018-4180-3. Epub 2019 Jan 4. Pediatr Nephrol. 2019. PMID: 30607568
Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract.
Madariaga L, García-Castaño A, Ariceta G, Martínez-Salazar R, Aguayo A, Castaño L; Spanish group for the study of HNF1B mutations. Madariaga L, et al. Clin Kidney J. 2018 Nov 13;12(3):373-379. doi: 10.1093/ckj/sfy102. eCollection 2019 Jun. Clin Kidney J. 2018. PMID: 31198537 Free PMC article.
Hypophosphataemic Rickets: Similar Phenotype of Different Diseases.
de la Cerda-Ojeda F, González-Rodríguez JD, Madariaga L, Martínez-Díaz-Guerra G, Matoses-Ruipérez ML. de la Cerda-Ojeda F, et al. Among authors: madariaga l. Adv Ther. 2020 May;37(Suppl 2):80-88. doi: 10.1007/s12325-019-01182-3. Epub 2020 Mar 31. Adv Ther. 2020. PMID: 32236875 Review.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Vall-Palomar M, Madariaga L, Ariceta G. Vall-Palomar M, et al. Among authors: madariaga l. Pediatr Nephrol. 2021 Oct;36(10):3045-3055. doi: 10.1007/s00467-021-04968-2. Epub 2021 Feb 17. Pediatr Nephrol. 2021. PMID: 33595712 Review.
60 results