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pregnancy combined with hydronephrosis相关文献:
Meta-analysis of second-trimester markers for trisomy 21.
Agathokleous M, Chaveeva P, Poon LC, Kosinski P, Nicolaides KH.
Ultrasound Obstet Gynecol. 2013 Mar;41(3):247-61. doi: 10.1002/uog.12364. Epub 2013 Jan 24.
PMID:23208748
Vesicoureteral Reflux.
Leslie SW, Aeddula NR.
2024 Apr 30. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–.
PMID:33085409
Hereditary Nephrogenic Diabetes Insipidus.
Knoers N, Lemmink H.
2000 Feb 12 [updated 2020 Feb 27]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
PMID:20301356
Percutaneous Nephrostomy.
Young M, Leslie SW.
2025 May 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–.
PMID:29630257
Successful treatment with radiation therapy for desmoid-type fibromatosis with unilateral hydronephrosis: a case report.
Ishikawa Y, Umezawa R, Yamamoto T, Takahashi N, Takeda K, Suzuki Y, Jingu K.
J Med Case Rep. 2021 Oct 27;15(1):540. doi: 10.1186/s13256-021-03088-7.
PMID:34702352
Vesico-ureteral reflux in children with prenatally detected hydronephrosis: a systematic review.
van Eerde AM, Meutgeert MH, de Jong TP, Giltay JC.
Ultrasound Obstet Gynecol. 2007 Apr;29(4):463-9. doi: 10.1002/uog.3975.
PMID:17390310
[Obstructive nephropathy].
Ringert RH, Riedmiller H, Rübben H, Rose A, Hoyer PF, Conrad S, Hoang-Böhm J, Müller-Wiefel DE.
Urologe A. 2006 Sep;45 Suppl 4:225-8. doi: 10.1007/s00120-006-1196-2.
PMID:16937123
Imaging the urinary tract.
Shackelford GD, Kees-Folts D, Cole BR.
Clin Perinatol. 1992 Mar;19(1):85-119.
PMID:1576776
Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype.
Verscaj CP, Gordon M, Holbrook BD, Trocki OM, Poorvu T, Miller C, Schwalbe T, Trout M, Zearfoss A, Welker A, Wojcik MH, Elias AF.
Am J Med Genet A. 2025 Aug;197(8):e64087. doi: 10.1002/ajmg.a.64087. Epub 2025 Apr 9.
PMID:40202083
Prenatal diagnosis of fetuses with renal abnormalities: a retrospective analysis of 329 Chinese cases.
Qin Y, Wang B, Zhu Y, Liu L, Liu N, Yao Y, Li H, Xu R, Zhang C, Song J.
Orphanet J Rare Dis. 2025 Sep 24;20(1):486. doi: 10.1186/s13023-025-04001-x.
PMID:40993696
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