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Progressive hydronephrosis, hydroureter, and dilatation of the bladder in siblings with congenital nephrogenic diabetes insipidus.

作者信息

Ten Bensel R W, Peters E R

出版信息

J Pediatr. 1970 Sep;77(3):439-43. doi: 10.1016/s0022-3476(70)80012-9.

DOI:10.1016/s0022-3476(70)80012-9
PMID:5502093
Abstract
摘要

相似文献

1
Progressive hydronephrosis, hydroureter, and dilatation of the bladder in siblings with congenital nephrogenic diabetes insipidus.先天性肾性尿崩症患儿同胞中出现的进行性肾积水、输尿管积水及膀胱扩张。
J Pediatr. 1970 Sep;77(3):439-43. doi: 10.1016/s0022-3476(70)80012-9.
2
[Functional dilatation of the upper urinary tract and bladder associated with nephrogenic diabetes insipidus].[与肾性尿崩症相关的上尿路和膀胱功能性扩张]
Minerva Pediatr. 1975 Jun 16;27(21):1213-7.
3
Nonobstructive urinary tract dilatation in children with diabetes insipidus.儿童尿崩症患者的非梗阻性尿路扩张。
J Pediatr Surg. 2012 Apr;47(4):752-5. doi: 10.1016/j.jpedsurg.2011.08.007.
4
Diabetes insipidus and nonobstructive dilation of urinary tract.尿崩症与非梗阻性尿路扩张。
Urology. 1980 Sep;16(3):266-9. doi: 10.1016/0090-4295(80)90039-4.
5
Congenital nephrogenic diabetes insipidus with bilateral hydronephrosis: indomethacin in treatment of nephrogenic diabetes insipidus.先天性肾性尿崩症伴双侧肾积水:吲哚美辛治疗肾性尿崩症
Yonsei Med J. 1980;21(2):116-22. doi: 10.3349/ymj.1980.21.2.116.
6
[Mega-ureter, mega-bladder and familial diabetes insipidus (author's transl)].[巨输尿管、巨膀胱与家族性尿崩症(作者译)]
Sem Hop. 1981;57(1-2):60-1.
7
Nephrogenic diabetes insipidus in a Negro kindred.一个黑人家族中的肾性尿崩症
Am J Dis Child. 1970 Jul;120(1):64-8. doi: 10.1001/archpedi.1970.02100060098016.
8
Hereditary nephrogenic diabetes insipidus and bilateral nonobstructive hydronephrosis.遗传性肾性尿崩症和双侧非梗阻性肾积水。
Nephron. 1993;65(3):346-9. doi: 10.1159/000187510.
9
[Familial diabetes insipidus, ureterohydronephrosis and terminal renal insufficiency].[家族性尿崩症、输尿管肾盂积水及终末期肾功能不全]
Rev Clin Esp. 1985 Jan;176(1):35-8.
10
Nephrogenic diabetes insipidus and obstructive uropathy.
Am J Dis Child. 1973 Sep;126(3):398-401. doi: 10.1001/archpedi.1973.02110190346021.

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1
Clinical and genetic analysis of X-linked nephrogenic diabetes insipidus caused by a novel mutation (NM_000054.6:exon3:c.245G>A (p.Cys82Tyr)) in a Chinese boy.一名中国男孩中由新突变(NM_000054.6:exon3:c.245G>A (p.Cys82Tyr))引起的X连锁肾性尿崩症的临床和遗传学分析
Intractable Rare Dis Res. 2025 Aug 31;14(3):216-222. doi: 10.5582/irdr.2025.01043.
2
CKD in a Young Man with Nephrogenic Diabetes Insipidus.一名患有肾性尿崩症的年轻男性的慢性肾脏病
Kidney360. 2025 Mar 1;6(3):482-483. doi: 10.34067/KID.0000000647.
3
Congenital nephrogenic diabetes insipidus presenting with bilateral hydronephrosis and dilatation of the ureter and bladder.
先天性肾性尿崩症伴双侧肾积水及输尿管和膀胱扩张。
Acute Med Surg. 2020 Oct 18;7(1):e579. doi: 10.1002/ams2.579. eCollection 2020 Jan-Dec.
4
Hypertensive urgency in nephrogenic diabetes insipidus with concomitant Hinman syndrome.伴有欣曼综合征的肾性尿崩症中的高血压急症
BMJ Case Rep. 2019 Jul 27;12(7):e229095. doi: 10.1136/bcr-2018-229095.
5
Clinical characteristics of eight patients with congenital nephrogenic diabetes insipidus.8例先天性肾性尿崩症患者的临床特征
Endocrine. 2004 Jun;24(1):55-9. doi: 10.1385/ENDO:24:1:055.
6
Investigation of the dilated urinary tract.扩张性尿路的检查
Pediatr Nephrol. 1988 Jan;2(1):43-7. doi: 10.1007/BF00870379.
7
Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment.肾性尿崩症:临床症状、发病机制、遗传学及治疗
Pediatr Nephrol. 1992 Sep;6(5):476-82. doi: 10.1007/BF00874020.
8
[Potomania: re-evaluation of the diagnostic tests and unusual presentation with hydronephrosis and megabladder].[水中毒:对诊断测试及肾积水和巨膀胱异常表现的重新评估]
Can Med Assoc J. 1977 Jun 18;116(12):1359-63.
9
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness. A clinical and genetic study.尿崩症、糖尿病、视神经萎缩和耳聋。一项临床与遗传学研究。
Postgrad Med J. 1979 Jun;55(644):377-80. doi: 10.1136/pgmj.55.644.377.