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renal malrotation相关文献:
Congenital Anomalies of the Upper Urinary Tract: A Comprehensive Review.
Houat AP, Guimarães CTS, Takahashi MS, Rodi GP, Gasparetto TPD, Blasbalg R, Velloni FG.
Radiographics. 2021 Mar-Apr;41(2):462-486. doi: 10.1148/rg.2021200078. Epub 2021 Jan 29.
PMID:33513074
SALL4-Related Disorders.
Kohlhase J.
2004 Aug 16 [updated 2022 Mar 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:20301547
Cyclic vomiting syndrome: A narrative review and guide to management.
Kovacic K, Li BUK.
Headache. 2021 Feb;61(2):231-243. doi: 10.1111/head.14073. Epub 2021 Feb 23.
PMID:33619730
KAT6B Disorders.
Lemire G, Campeau PM, Lee BH.
2012 Dec 13 [updated 2020 Jan 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:23236640
SALL1-Related Townes-Brocks Syndrome.
Graziano C, Olivucci G.
2007 Jan 24 [updated 2024 Aug 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:20301618
ACTG2 Visceral Myopathy.
Bhagwat PK, Wangler MF.
2015 Jun 11 [updated 2021 May 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:26072522
Mimics of malrotation on pediatric upper gastrointestinal series: a pictorial review.
Smitthimedhin A, Suarez A, Webb RL, Otero HJ.
Abdom Radiol (NY). 2018 Sep;43(9):2246-2254. doi: 10.1007/s00261-018-1537-9.
PMID:29500650
MYRF-Related Cardiac Urogenital Syndrome.
Kaplan JD, Stewart B, Prasov L, Pyle LC.
2022 Nov 10. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:36375006
CTCF-Related Disorder.
Valverde de Morales HG, Wang HL, Garber K, Corces V, Li H.
2024 Apr 25. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:38662876
Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities.
Lavillaureix A, Foulon G, Launay E, Belaud-Rotureau MA, Thibault R, Lambe C, Aussel D, Pasquier L, Odent S, Arnaud A, Habonimana E, Dabadie A, Jaillard S.
Clin Res Hepatol Gastroenterol. 2021 Sep;45(5):101562. doi: 10.1016/j.clinre.2020.10.007. Epub 2020 Nov 15.
PMID:33208297
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