Suppr超能文献

相似文献

1
Dent's disease complicated by nephrotic syndrome: A case report.
Intractable Rare Dis Res. 2016 Nov;5(4):297-300. doi: 10.5582/irdr.2016.01058.
2
A rare case of nephrotic syndrome associated with Dent's disease: a case report.
CEN Case Rep. 2020 Nov;9(4):380-384. doi: 10.1007/s13730-020-00491-9. Epub 2020 Jun 12.
3
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
Kidney Int. 2000 Jan;57(1):240-9. doi: 10.1046/j.1523-1755.2000.00847.x.
4
[A rare tubulopathy: Dent's disease in the background of focal segmental glomerular sclerosis].
Orv Hetil. 2023 May 21;164(20):788-791. doi: 10.1556/650.2023.32787.
5
Dent's disease.
Orphanet J Rare Dis. 2010 Oct 14;5:28. doi: 10.1186/1750-1172-5-28.
6
An atypical Dent's disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes.
Eur J Hum Genet. 2013 Jun;21(6):687-90. doi: 10.1038/ejhg.2012.225. Epub 2012 Oct 10.
7
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations.
Pediatr Nephrol. 2009 Oct;24(10):1967-73. doi: 10.1007/s00467-009-1228-4. Epub 2009 Jul 7.
8
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?
Pediatr Nephrol. 2009 Dec;24(12):2369-73. doi: 10.1007/s00467-009-1299-2.
9
Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis.
Kidney Int. 2000 Mar;57(3):787-93. doi: 10.1046/j.1523-1755.2000.00916.x.
10
Genetic Analysis of Dent's Disease and Functional Research of CLCN5 Mutations.
DNA Cell Biol. 2017 Dec;36(12):1151-1158. doi: 10.1089/dna.2017.3731. Epub 2017 Oct 23.

引用本文的文献

2
Look Alike, Sound Alike: Phenocopies in Steroid-Resistant Nephrotic Syndrome.
Int J Environ Res Public Health. 2020 Nov 12;17(22):8363. doi: 10.3390/ijerph17228363.
3
A rare case of nephrotic syndrome associated with Dent's disease: a case report.
CEN Case Rep. 2020 Nov;9(4):380-384. doi: 10.1007/s13730-020-00491-9. Epub 2020 Jun 12.
5
Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case Reports.
Front Med (Lausanne). 2018 Dec 7;5:347. doi: 10.3389/fmed.2018.00347. eCollection 2018.

本文引用的文献

2
Urinary α -microglobulin and albumin excretion in children and adolescents with type 1 diabetes.
J Diabetes. 2017 Jan;9(1):61-64. doi: 10.1111/1753-0407.12383. Epub 2016 Mar 16.
3
Dent disease in children: diagnostic and therapeutic considerations.
Clin Nephrol. 2015 Oct;84(4):222-30. doi: 10.5414/CN108522.
4
Nephrotic-range Albuminuria as the presenting symptom of Dent-2 disease.
Ital J Pediatr. 2015 Jun 25;41:46. doi: 10.1186/s13052-015-0152-4.
5
Urine retinol-binding protein 4: a functional biomarker of the proximal renal tubule.
Adv Clin Chem. 2014;63:85-122. doi: 10.1016/b978-0-12-800094-6.00003-0.
6
The cellular and physiological functions of the Lowe syndrome protein OCRL1.
Traffic. 2014 May;15(5):471-87. doi: 10.1111/tra.12160. Epub 2014 Mar 7.
9
Dent's disease.
Orphanet J Rare Dis. 2010 Oct 14;5:28. doi: 10.1186/1750-1172-5-28.
10
Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?
Pediatr Nephrol. 2009 Dec;24(12):2369-73. doi: 10.1007/s00467-009-1299-2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验