Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/72932
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Robayna, S. Marrero | en_US |
dc.contributor.author | Cascón, L. Hortal | en_US |
dc.contributor.author | Díaz, N. Vega | en_US |
dc.contributor.author | Pérez, J. C.Rodríguez | en_US |
dc.date.accessioned | 2020-06-03T12:44:42Z | - |
dc.date.available | 2020-06-03T12:44:42Z | - |
dc.date.issued | 2015 | en_US |
dc.identifier.issn | 0304-5412 | en_US |
dc.identifier.other | Scopus | - |
dc.identifier.uri | http://hdl.handle.net/10553/72932 | - |
dc.description.abstract | En esta unidad de actualización se estudian las alteraciones renales congénitas y hereditarias. Considerando las alteraciones congénitas aquellas que se manifiestan o existen desde el nacimiento, pero que han sido adquiridas por el feto durante su periodo intraútero, a efectos de diferenciarlas de aquellas que son hereditarias, que se transmiten a través de anomalías cromosómicas y con repercusión sobre la familia. Dentro de las anomalías congénitas, los autores presentan las malformaciones más frecuentes tanto del parénquima renal como de la vía urinaria. Entre las últimas, incluiremos las enfermedades quísticas y aquellas con daño predominantemente glomerular o tubulointersticial. | en_US |
dc.description.abstract | Congenital and hereditary renal alterations are studied in this unit of update. Where as the congenital disorders that manifest them selves came from birth, which have been purchase d by the fetus during the prenatal period, we must distinguish them from those that are inherited, which is transmitted through chromosomal abnormalities and with a deep impact on the family. Within the congenital anomalies, the authors present the more frequent malformations already of the renal parenchyma, already of the urinary tract. Among the latter, we will include cystic diseases and those with predominantly glomerular or tubulo-interstitial damage. | en_US |
dc.language | spa | en_US |
dc.relation.ispartof | Medicine | en_US |
dc.source | Medicine (Spain) [ISSN 0304-5412], v. 11 (80), p. 4793-4802, (Mayo 2015) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject.other | Nefropatías congénitas | en_US |
dc.subject.other | Nefropatías hereditarias | en_US |
dc.subject.other | Nefropatías quísticas | en_US |
dc.subject.other | Alport | en_US |
dc.subject.other | Fabry | en_US |
dc.title | Nefropatías hereditarias y congénitas | en_US |
dc.title.alternative | Hereditary and congenital nephropathy | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.med.2015.05.020 | en_US |
dc.identifier.scopus | 84944749144 | - |
dc.contributor.authorscopusid | 56913428800 | - |
dc.contributor.authorscopusid | 55096931600 | - |
dc.contributor.authorscopusid | 56912987500 | - |
dc.contributor.authorscopusid | 57207052743 | - |
dc.identifier.eissn | 1578-8822 | - |
dc.description.lastpage | 4802 | en_US |
dc.identifier.issue | 80 | - |
dc.description.firstpage | 4793 | en_US |
dc.relation.volume | 11 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 9 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Mayo 2015 | en_US |
dc.identifier.ulpgc | Sí | es |
dc.description.sjr | 0,108 | |
dc.description.sjrq | Q4 | |
item.fulltext | Sin texto completo | - |
item.grantfulltext | none | - |
Appears in Collections: | Artículos |
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