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1
Could This Be Alport Syndrome?
Clin J Am Soc Nephrol. 2021 Nov;16(11):1743-1745. doi: 10.2215/CJN.00120121. Epub 2021 Apr 13.
2
Guidelines for Genetic Testing and Management of Alport Syndrome.
Clin J Am Soc Nephrol. 2022 Jan;17(1):143-154. doi: 10.2215/CJN.04230321. Epub 2021 Dec 20.
3
Alport Syndrome: Achieving Early Diagnosis and Treatment.
Am J Kidney Dis. 2021 Feb;77(2):272-279. doi: 10.1053/j.ajkd.2020.03.026. Epub 2020 Jul 22.
4
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
Clin J Am Soc Nephrol. 2016 Aug 8;11(8):1441-1449. doi: 10.2215/CJN.01000116. Epub 2016 Jun 8.
5
Clinical utility gene card for: Alport syndrome - update 2014.
Eur J Hum Genet. 2015 Sep;23(9). doi: 10.1038/ejhg.2014.254. Epub 2014 Nov 12.
6
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
Pediatr Nephrol. 2020 Oct;35(10):1941-1952. doi: 10.1007/s00467-020-04574-8. Epub 2020 May 11.
7
Endothelial cell-specific collagen type IV-α expression does not rescue Alport syndrome in Col4a3 mice.
Am J Physiol Renal Physiol. 2019 May 1;316(5):F830-F837. doi: 10.1152/ajprenal.00556.2018. Epub 2019 Feb 6.
9
Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study.
Am J Kidney Dis. 2021 Oct;78(4):560-570.e1. doi: 10.1053/j.ajkd.2021.02.326. Epub 2021 Apr 7.
10
[Research progress in diagnosis, treatment and management of Alport syndrome].
Zhonghua Er Ke Za Zhi. 2022 Apr 2;60(4):370-373. doi: 10.3760/cma.j.cn112140-20210907-00759.

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