首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
xanthinuria相关文献:
Xanthinuria secondary to allopurinol treatment in dogs with leishmaniosis: Current perspectives of the Iberian veterinary community.
Jesus L, Arenas C, Domínguez-Ruiz M, Silvestrini P, Englar RE, Roura X, Leal RO.
Comp Immunol Microbiol Infect Dis. 2022 Apr;83:101783. doi: 10.1016/j.cimid.2022.101783. Epub 2022 Feb 24.
PMID:35240487
Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine Oxidoreductase.
Sekine M, Okamoto K, Ichida K.
Biomedicines. 2021 Nov 20;9(11):1723. doi: 10.3390/biomedicines9111723.
PMID:34829959
Xanthinuria.
DICKINSON CJ, SMELLIE JM.
Br Med J. 1959 Dec 5;2(5161):1217-21. doi: 10.1136/bmj.2.5161.1217.
PMID:13816599
Xanthinuria and pregnancy.
McKeran RO.
Lancet. 1977 Jul 9;2(8028):86-7. doi: 10.1016/s0140-6736(77)90086-1.
PMID:69167
XANTHINURIA AND HEMOCHROMATOSIS.
AYVAZIAN JH.
N Engl J Med. 1964 Jan 2;270:18-22. doi: 10.1056/NEJM196401022700104.
PMID:14062123
Candidate causative variant for xanthinuria in a Domestic Shorthair cat.
Pritchard E, Samaha G, Mizzi K, Boland L; 99Lives Consortium; Haase B.
Anim Genet. 2023 Aug;54(4):576-580. doi: 10.1111/age.13318. Epub 2023 Mar 27.
PMID:36970934
Fortuitous Discovery of Hereditary Xanthinuria.
Biaz A, Tazi S, Bouhsain S, Chemsi M, Dami A, Machtani-Idrissi SE.
Clin Lab. 2020 Oct 1;66(10). doi: 10.7754/Clin.Lab.2020.200253.
PMID:33073950
Hereditary xanthinuria in a goat.
Vail KJ, Tate NM, Likavec T, Minor KM, Gibbons PM, Rech RR, Furrow E.
J Vet Intern Med. 2019 Mar;33(2):1009-1014. doi: 10.1111/jvim.15431. Epub 2019 Feb 13.
PMID:30758870
[Xanthinuria].
Homma S, Asano Y.
Ryoikibetsu Shokogun Shirizu. 1997;(17 Pt 2):269-72.
PMID:9277914
Asymptomatic hereditary xanthinuria: a case report.
Nagae A, Murakami E, Hiwada K, Sato Y, Kawachi M, Kono N.
Jpn J Med. 1990 May-Jun;29(3):287-91. doi: 10.2169/internalmedicine1962.29.287.
PMID:2273608
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3