Autosomal Dominant Polycystic Kidney Disease: Core Curriculum 2016.
作者信息
Chebib Fouad T, Torres Vicente E
机构信息
Mayo Clinic College of Medicine, Rochester, MN.
Mayo Clinic College of Medicine, Rochester, MN.
出版信息
Am J Kidney Dis. 2016 May;67(5):792-810. doi: 10.1053/j.ajkd.2015.07.037. Epub 2015 Oct 31.
Abstract
摘要
相似文献
1
Autosomal Dominant Polycystic Kidney Disease: Core Curriculum 2016.常染色体显性多囊肾病：2016年核心课程
Am J Kidney Dis. 2016 May;67(5):792-810. doi: 10.1053/j.ajkd.2015.07.037. Epub 2015 Oct 31.
2
Autosomal dominant polycystic kidney disease.常染色体显性多囊肾病。
Am Fam Physician. 2014 Sep 1;90(5):303-7.
3
Recent advances in autosomal-dominant polycystic kidney disease.常染色体显性遗传性多囊肾病的最新进展。
Intern Med J. 2016 Aug;46(8):883-92. doi: 10.1111/imj.13143.
4
[Renal manifestation of Autosomal Dominant Polycystic Kidney Disease].常染色体显性多囊肾病的肾脏表现
G Ital Nefrol. 2018 Mar;35(2).
5
Detection of autosomal dominant polycystic kidney disease by NMR spectroscopic fingerprinting of urine.尿液核磁共振谱指纹分析检测常染色体显性多囊肾病。
Kidney Int. 2011 Jun;79(11):1244-53. doi: 10.1038/ki.2011.30. Epub 2011 Mar 9.
6
Molecular pathways and therapies in autosomal-dominant polycystic kidney disease.常染色体显性多囊肾病的分子途径与治疗方法
Physiology (Bethesda). 2015 May;30(3):195-207. doi: 10.1152/physiol.00032.2014.
7
[Autosome dominant polycystic kidney disease. Leading symptoms: arterial hypertension, flank/back/abdominal pain, hematuria, renal failure].[常染色体显性多囊肾病。主要症状：动脉高血压、胁腹/背部/腹痛、血尿、肾衰竭]
Praxis (Bern 1994). 2004 Nov 24;93(48):1993-7; quiz 1998. doi: 10.1024/0369-8394.93.48.1993.
8
Autosomal dominant polycystic kidney disease: Study of clinical characteristics in an Indian population.常染色体显性多囊肾病：印度人群临床特征研究
Saudi J Kidney Dis Transpl. 2017 Jan-Feb;28(1):115-124. doi: 10.4103/1319-2442.198163.
9
KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.KHA-CARI常染色体显性多囊肾病诊断与管理指南建议
Nephrology (Carlton). 2016 Aug;21(8):705-16. doi: 10.1111/nep.12658.
10
Simultaneous adult polycystic kidney disease and Alport syndrome.成人多囊肾病与奥尔波特综合征并存。
Nephrology (Carlton). 2016 Aug;21(8):722-3. doi: 10.1111/nep.12661.
引用本文的文献
1
Acute Tubulointerstitial Nephritis (ATIN) in Patient With Autosomal Dominant Polycystic Kidney Disease (ADPKD): A Case Report.常染色体显性多囊肾病（ADPKD）患者的急性肾小管间质性肾炎（ATIN）：一例报告
Case Rep Nephrol. 2025 Aug 23;2025:3069446. doi: 10.1155/crin/3069446. eCollection 2025.
2
Characterizing the ADPKD- Phenotypic Signature With Deep Learning and Advanced Imaging Biomarkers.利用深度学习和先进成像生物标志物表征常染色体显性多囊肾病的表型特征。
Kidney Int Rep. 2025 May 7;10(8):2690-2707. doi: 10.1016/j.ekir.2025.04.062. eCollection 2025 Aug.
3
Rag GTPases Suppress Renal Cystic Disease by Inhibiting TFEB Independently of mTORC1.Rag GTP酶通过独立于mTORC1抑制转录因子EB来抑制肾囊性疾病。
bioRxiv. 2025 Jul 31:2025.07.24.664930. doi: 10.1101/2025.07.24.664930.
4
Prenatal Diagnosis of Autosomal Dominant Polycystic Kidney Disease: Case Report.常染色体显性多囊肾病的产前诊断：病例报告
Reports (MDPI). 2025 Apr 23;8(2):56. doi: 10.3390/reports8020056.
5
Family Planning in Patients With ADPKD-Results From the DIPAK Consortium.常染色体显性多囊肾病患者的计划生育——来自DIPAK联盟的结果
Kidney Int Rep. 2025 Mar 13;10(6):1843-1854. doi: 10.1016/j.ekir.2025.03.004. eCollection 2025 Jun.
6
Bilateral nephrectomy in autosomal dominant polycystic kidney disease patients before or after renal transplantation: data from a retrospective cohort study.常染色体显性多囊肾病患者肾移植前后的双侧肾切除术：一项回顾性队列研究的数据
Clin Kidney J. 2025 May 20;18(6):sfaf155. doi: 10.1093/ckj/sfaf155. eCollection 2025 Jun.
7
Autosomal Dominant Polycystic Kidney Disease Patients Requiring Nephrectomy: Characteristics and Surgical Considerations.需要肾切除术的常染色体显性多囊肾病患者：特征与手术考量
ANZ J Surg. 2025 Jul-Aug;95(7-8):1605-1616. doi: 10.1111/ans.70192. Epub 2025 Jun 18.
8
Ciliary G-Protein Coupled Receptor Signaling in Polycystic Kidney Disease.多囊肾病中的纤毛G蛋白偶联受体信号传导
Int J Mol Sci. 2025 May 22;26(11):4971. doi: 10.3390/ijms26114971.
9
Pathogenic variants in the polycystin pore helix cause distinct forms of channel dysfunction.多囊蛋白孔螺旋中的致病性变异会导致不同形式的通道功能障碍。
Proc Natl Acad Sci U S A. 2025 Jun 17;122(24):e2421362122. doi: 10.1073/pnas.2421362122. Epub 2025 Jun 12.
10
Deciphering Intercellular Communication of the Immune Landscape within Autosomal Dominant Polycystic Kidney Disease Microenvironment at Single-Cell Resolution.以单细胞分辨率解析常染色体显性多囊肾病微环境中免疫格局的细胞间通讯
Kidney Dis (Basel). 2025 Apr 6;11(1):302-318. doi: 10.1159/000545663. eCollection 2025 Jan-Dec.
Zotero 插件