Coto E - Search Results

1

Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing.

Gómez J, Gil-Peña H, Santos F, Coto E, Arango A, Hernandez O, Rodríguez J, Nadal I, Cantos V, Chocrón S, Vergara I, Madrid Á, Vazquez C, González LE, Blanco F. Gómez J, et al. Among authors: coto e. Pediatr Res. 2016 Mar;79(3):496-501. doi: 10.1038/pr.2015.243. Epub 2015 Nov 16. Pediatr Res. 2016. PMID: 26571219 Free article.

2

Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: juvenile and adult onset.

López-Larrea C, Gonzalez-Roces S, Peña M, Dominguez O, Coto E, Alvarez V, Moreno M, Hernandez O, Burgos-Vargas R, Gorodezky C. López-Larrea C, et al. Among authors: coto e. Hum Immunol. 1995 Jul;43(3):174-80. doi: 10.1016/0198-8859(94)00156-k. Hum Immunol. 1995. PMID: 7558934

3

A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies.

Coto E, Rodriguez J, Jeck N, Alvarez V, Stone R, Loris C, Rodriguez LM, Fischbach M, Seyberth HW, Santos F. Coto E, et al. Kidney Int. 2004 Jan;65(1):25-9. doi: 10.1111/j.1523-1755.2004.00388.x. Kidney Int. 2004. PMID: 14675033 Free article.

4

Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children.

Gil H, Santos F, García E, Alvarez MV, Ordóñez FA, Málaga S, Coto E. Gil H, et al. Among authors: coto e. Pediatr Nephrol. 2007 Jun;22(6):825-8. doi: 10.1007/s00467-006-0417-7. Epub 2007 Jan 11. Pediatr Nephrol. 2007. PMID: 17216496

5

Clinical and analytical findings in Gitelman's syndrome associated with homozygosity for the c.1925 G>A SLC12A3 mutation.

Coto E, Arriba G, García-Castro M, Santos F, Corao AI, Díaz M, Sánchez Heras M, Basterrechea MA, Tallón S, Alvarez V. Coto E, et al. Am J Nephrol. 2009;30(3):218-21. doi: 10.1159/000218104. Epub 2009 May 7. Am J Nephrol. 2009. PMID: 19420906

6

[Magnesium homeostasis. Etiopathogeny, clinical diagnosis and treatment of hypomagnesaemia. A case study].

González EP, Santos F, Coto E. González EP, et al. Among authors: coto e. Nefrologia. 2009;29(6):518-24. doi: 10.3265/Nefrologia.2009.29.6.5534.en.full. Nefrologia. 2009. PMID: 19935995 Free article. Review. Spanish.

7

Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report.

Mejia-Gaviria N, Gil-Peña H, Coto E, Pérez-Menéndez TM, Santos F. Mejia-Gaviria N, et al. Among authors: coto e. Orphanet J Rare Dis. 2010 Jan 14;5:1. doi: 10.1186/1750-1172-5-1. Orphanet J Rare Dis. 2010. PMID: 20074341 Free PMC article.

8

Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life.

Herrero-Morín JD, Rodríguez J, Coto E, Gil-Peña H, Alvarez V, Espinosa L, Loris C, Gil-Calvo M, Santos F. Herrero-Morín JD, et al. Among authors: coto e. Nephrol Dial Transplant. 2011 Jan;26(1):151-5. doi: 10.1093/ndt/gfq352. Epub 2010 Jun 22. Nephrol Dial Transplant. 2011. PMID: 20571093

9

Common European mitochondrial haplogroups in the risk for psoriasis and psoriatic arthritis.

Coto-Segura P, Santos-Juanes J, Gómez J, Alvarez V, Díaz M, Alonso B, Corao AI, Coto E. Coto-Segura P, et al. Among authors: coto e. Genet Test Mol Biomarkers. 2012 Jun;16(6):621-3. doi: 10.1089/gtmb.2011.0266. Epub 2011 Dec 22. Genet Test Mol Biomarkers. 2012. PMID: 22191676

10

Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes.

Eiris N, Santos-Juanes J, Coto-Segura P, Gómez J, Alvarez V, Morales B, Queiro R, Díaz M, Corao AI, López-Corte K, Coto E. Eiris N, et al. Among authors: coto segura p, coto e. Cytokine. 2012 Oct;60(1):27-9. doi: 10.1016/j.cyto.2012.05.030. Epub 2012 Jun 26. Cytokine. 2012. PMID: 22739501

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