Revisión de la nefropatía tubulointersticial autosómica dominante
Nefrología, ISSN: 0211-6995, Vol: 37, Issue: 3, Page: 235-243
2017
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- 48Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
En los últimos años ha habido una reclasificación de las nefropatías tubulointersticiales de base genética. Los antiguos conceptos de nefronoptisis o enfermedad quística medular han sido reordenados con base en el hallazgo de nuevos genes. Las guías KDIGO del 2015 proponen una unificación de terminología, unos criterios diagnósticos y de seguimiento. Hasta el momento se han descrito 4 genes causantes de la nefropatía tubulointersticial autosómica dominante: MUC1, UMOD, HNF1B y REN. Aunque la mutación en cada uno de los genes produce unos rasgos diferenciales en la forma de presentación, todas las formas tienen en común el progresivo daño túbulo-intersticial y la fibrosis renal. En este artículo, se pretende una revisión de las guías, de la literatura y ofrecer unas recomendaciones prácticas para el manejo de esta enfermedad.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0211699516301989; http://dx.doi.org/10.1016/j.nefro.2016.10.024; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85021283195&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28648202; https://linkinghub.elsevier.com/retrieve/pii/S0211699516301989; http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952017000300235&lng=en&tlng=en; http://scielo.isciii.es/scielo.php?script=sci_abstract&pid=S0211-69952017000300235&lng=en&tlng=en; http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952017000300235; http://scielo.isciii.es/scielo.php?script=sci_abstract&pid=S0211-69952017000300235; https://dx.doi.org/10.1016/j.nefro.2016.10.024
Elsevier BV
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