Renal tubular disorders.
作者信息
Walsh Stephen B, Unwin Robert J
机构信息
UCL Centre for Nephrology, Royal Free Campus and Hospital, University College London Medical School.
出版信息
Clin Med (Lond). 2012 Oct;12(5):476-9. doi: 10.7861/clinmedicine.12-5-476.
Abstract
摘要
相似文献
1
Renal tubular disorders.肾小管疾病
Clin Med (Lond). 2012 Oct;12(5):476-9. doi: 10.7861/clinmedicine.12-5-476.
2
[Progress in study of impaired water excretion].[水排泄障碍的研究进展]
Nihon Naika Gakkai Zasshi. 2006 May 10;95(5):814-20. doi: 10.2169/naika.95.814.
3
[Non-lithiasic hereditary tubulopathies].[非结石性遗传性肾小管病]
Rev Prat. 1997 Sep 15;47(14):1559-65.
4
Molecular pathophysiology of inborn renal Na+ transport defects.先天性肾钠转运缺陷的分子病理生理学
Kidney Blood Press Res. 1998;21(2-4):222-5. doi: 10.1159/000025860.
5
Monogenic tubular salt and acid transporter disorders.单基因肾小管盐和酸转运体疾病
J Nephrol. 2002 Nov-Dec;15 Suppl 6:S57-68.
6
Inherited tubule disorders.
Hosp Pract (Off Ed). 1982 Feb;17(2):111-7, 121-8. doi: 10.1080/21548331.1982.11698048.
7
Biology and genetics of inherited renal tubular disorders.遗传性肾小管疾病的生物学与遗传学
Exp Nephrol. 1996 Sep-Oct;4(5):253-62.
8
A female with X-linked Nephrogenic diabetes insipidus in a family with inherited central diabetes Insipidus: Case report and review of the literature.家族性中枢性尿崩症伴 X 连锁遗传性肾性尿崩症女性：病例报告及文献复习。
Am J Med Genet A. 2020 May;182(5):1032-1040. doi: 10.1002/ajmg.a.61516. Epub 2020 Feb 19.
9
Hypouricemia due to isolated renal tubular defect. Dalmatian dog mutation in man.孤立性肾小管缺陷导致的低尿酸血症。人类的达尔马提亚犬突变。
Am J Med. 1972 Sep;53(3):361-7. doi: 10.1016/0002-9343(72)90181-7.
10
Nephrogenic syndrome of inappropriate antidiuresis (NSIAD): a paradigm for activating mutations causing endocrine dysfunction.肾源性抗利尿激素分泌不当综合征（NSIAD）：激活突变导致内分泌功能障碍的范例。
Pediatr Endocrinol Rev. 2006 Dec;4 Suppl 1:66-70.
引用本文的文献
1
Probing the microRNA landscape in cadmium chloride induced renal toxicity through an in silico approach.通过计算机模拟方法探究氯化镉诱导的肾毒性中的微小RNA情况。
Sci Rep. 2025 Jul 12;15(1):25251. doi: 10.1038/s41598-025-11473-1.
2
Effects of Lebanese Folk Herbs on Adult Male Rats: Hepatic and Renal Toxicity, Histological, and Biochemical Studies.黎巴嫩民间草药对成年雄性大鼠的影响：肝脏和肾脏毒性、组织学及生化研究
Nutrients. 2025 Feb 28;17(5):875. doi: 10.3390/nu17050875.
3
Heavy metals: toxicity and human health effects.重金属：毒性与对人类健康的影响
Arch Toxicol. 2025 Jan;99(1):153-209. doi: 10.1007/s00204-024-03903-2. Epub 2024 Nov 20.
4
Untangling the Uncertain Role of Overactivation of the Renin-Angiotensin-Aldosterone System with the Aging Process Based on Sodium Wasting Human Models.基于钠耗竭人类模型探讨肾素-血管紧张素-醛固酮系统过度激活与衰老过程的不确定作用。
Int J Mol Sci. 2024 Aug 28;25(17):9332. doi: 10.3390/ijms25179332.
5
X-Ray-Based 3D Histopathology of the Kidney Using Cryogenic Contrast-Enhanced MicroCT.使用低温增强对比显微CT的基于X射线的肾脏三维组织病理学
Int J Biomed Imaging. 2024 Apr 9;2024:3924036. doi: 10.1155/2024/3924036. eCollection 2024.
6
A Case of Light Chain Deposition Disease Leading to Acute Liver Failure and Review of Literature.一例导致急性肝衰竭的轻链沉积病病例及文献综述
Diseases. 2023 Feb 1;11(1):24. doi: 10.3390/diseases11010024.
7
Immunopathology of Renal Tissue in Fatal Cases of Dengue in Children.儿童登革热致死病例的肾组织免疫病理学
Pathogens. 2022 Dec 15;11(12):1543. doi: 10.3390/pathogens11121543.
8
Kctd15 regulates nephron segment development by repressing Tfap2a activity.Kctd15 通过抑制 Tfap2a 的活性来调节肾单位节段的发育。
Development. 2020 Dec 14;147(23):dev191973. doi: 10.1242/dev.191973.
9
Hnf4a Is Required for the Development of Cdh6-Expressing Progenitors into Proximal Tubules in the Mouse Kidney.Hnf4a 对于将 Cd h6 表达祖细胞发育为小鼠肾脏近曲小管是必需的。
J Am Soc Nephrol. 2020 Nov;31(11):2543-2558. doi: 10.1681/ASN.2020020184. Epub 2020 Aug 6.
10
Hnf4a deletion in the mouse kidney phenocopies Fanconi renotubular syndrome.小鼠肾脏中 Hnf4a 的缺失可模拟法布里肾 tubular 综合征。
JCI Insight. 2018 Jul 26;3(14). doi: 10.1172/jci.insight.97497.
本文引用的文献
1
A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia.渗透压调节性瞬时受体电位香草酸亚型4（TRPV4）基因的功能丧失性非同义多态性与人类低钠血症相关。
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):14034-9. doi: 10.1073/pnas.0904084106. Epub 2009 Aug 4.
2
Amiloride blocks lithium entry through the sodium channel thereby attenuating the resultant nephrogenic diabetes insipidus.氨氯地平可阻止锂通过钠通道进入，从而减轻由此导致的肾性尿崩症。
Kidney Int. 2009 Jul;76(1):44-53. doi: 10.1038/ki.2009.91. Epub 2009 Apr 15.
3
An improved terminology and classification of Bartter-like syndromes.巴特综合征样疾病的术语和分类的改进
Nat Clin Pract Nephrol. 2008 Oct;4(10):560-7. doi: 10.1038/ncpneph0912. Epub 2008 Aug 12.
4
Urinary acidification assessed by simultaneous furosemide and fludrocortisone treatment: an alternative to ammonium chloride.通过速尿和氟氢可的松联合治疗评估尿酸化：氯化铵的替代方法。
Kidney Int. 2007 Jun;71(12):1310-6. doi: 10.1038/sj.ki.5002220. Epub 2007 Apr 4.
5
Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease.一例遗传性远端肾小管酸中毒（伴有独特的AE1突变）与自身免疫性疾病继发的获得性病例的免疫组织化学比较。
Nephrol Dial Transplant. 2007 Mar;22(3):807-12. doi: 10.1093/ndt/gfl662. Epub 2007 Jan 5.
6
Nephrogenic syndrome of inappropriate antidiuresis.肾源性抗利尿激素分泌异常综合征
N Engl J Med. 2005 May 5;352(18):1884-90. doi: 10.1056/NEJMoa042743.
7
Dent Disease with mutations in OCRL1.伴有OCRL1基因突变的丹特病
Am J Hum Genet. 2005 Feb;76(2):260-7. doi: 10.1086/427887. Epub 2004 Dec 30.
8
Wilson's disease and the Fanconi syndrome.威尔逊病与范科尼综合征。
Q J Med. 1962 Jul;31:361-84.
9
The excretion of acid in renal disease.肾脏疾病中的酸排泄
Q J Med. 1959 Apr;28(110):259-313.
10
Fanconi syndrome and renal failure induced by tenofovir: a first case report.替诺福韦所致范科尼综合征和肾衰竭：首例病例报告。
Am J Kidney Dis. 2002 Dec;40(6):1331-3. doi: 10.1053/ajkd.2002.36924.
Zotero 插件