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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 2
1985 1
2001 1
2002 1
2007 1
2008 2
2009 1
2010 1
2011 2
2016 1
2017 1
2024 0

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14 results

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Page 1
[Acute scrotum and Schönlein-Henoch purpura: report of 2 new cases].
Gómez Parada J, Puyol Pallás M, Vila Cots J, Comesías González MJ, Gallastegui Dañobeitia JC. Gómez Parada J, et al. Among authors: vila cots j. Arch Esp Urol. 2001 Mar;54(2):168-70. Arch Esp Urol. 2001. PMID: 11341123 Review. Spanish.
Pseudohypoaldosteronism types I and II: little more than a name in common.
Casas-Alba D, Vila Cots J, Monfort Carretero L, Martorell Sampol L, Zennaro MC, Jeunemaitre X, Camacho Díaz JA. Casas-Alba D, et al. Among authors: vila cots j. J Pediatr Endocrinol Metab. 2017 May 1;30(5):597-601. doi: 10.1515/jpem-2016-0467. J Pediatr Endocrinol Metab. 2017. PMID: 28593901
[Hemolytic-uraemic syndrome. A review of 58 cases].
Giménez Llort A, Camacho Díaz JA, Vila Cots J, Vila Santandreu A, Jordán García Y, Palomeque Rico A, Suñol Capella M. Giménez Llort A, et al. Among authors: vila cots j. An Pediatr (Barc). 2008 Oct;69(4):297-303. doi: 10.1157/13126552. An Pediatr (Barc). 2008. PMID: 18928695 Free article. Spanish.
Nephrotic syndrome associated with Celiac disease. A report of five cases.
Gimenez Llort A, Vila Cots J, Camacho Diaz JA, Vila Santandreu A, Concheiro Guisan A, Garcia Garcia L. Gimenez Llort A, et al. Among authors: vila cots j. Nephron. 2002 Dec;92(4):950. doi: 10.1159/000065576. Nephron. 2002. PMID: 12399649 Free article. No abstract available.
Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
Santín S, García-Maset R, Ruíz P, Giménez I, Zamora I, Peña A, Madrid A, Camacho JA, Fraga G, Sánchez-Moreno A, Cobo MA, Bernis C, Ortiz A, de Pablos AL, Pintos G, Justa ML, Hidalgo-Barquero E, Fernández-Llama P, Ballarín J, Ars E, Torra R; FSGS Spanish Study Group. Santín S, et al. Kidney Int. 2009 Dec;76(12):1268-76. doi: 10.1038/ki.2009.381. Epub 2009 Oct 7. Kidney Int. 2009. PMID: 19812541 Free article.
[Pneumonia associated acute glomerulonephritis: a review of 6 cases].
Vila Cots J, Piqueras Marimbaldo I, Arias Constanti V, Camacho Díaz JA, Gimenez Llort A, Vila Santandreu A, Ramos Cebrian M. Vila Cots J, et al. An Pediatr (Barc). 2011 May;74(5):332-5. doi: 10.1016/j.anpedi.2010.10.019. Epub 2011 Feb 18. An Pediatr (Barc). 2011. PMID: 21334269 Free article. Spanish.
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.
Morey M, Castro-Feijóo L, Barreiro J, Cabanas P, Pombo M, Gil M, Bernabeu I, Díaz-Grande JM, Rey-Cordo L, Ariceta G, Rica I, Nieto J, Vilalta R, Martorell L, Vila-Cots J, Aleixandre F, Fontalba A, Soriano-Guillén L, García-Sagredo JM, García-Miñaur S, Rodríguez B, Juaristi S, García-Pardos C, Martínez-Peinado A, Millán JM, Medeira A, Moldovan O, Fernandez A, Loidi L. Morey M, et al. Among authors: vila cots j. BMC Med Genet. 2011 Sep 8;12:116. doi: 10.1186/1471-2350-12-116. BMC Med Genet. 2011. PMID: 21902834 Free PMC article.
14 results