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hereditary xanthinuria相关文献:
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
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
Hypouricaemia in a patient with hereditary xanthinuria type I.
Maes B, Dedeurwaerdere F.
Lancet. 2024 Apr 13;403(10435):1493. doi: 10.1016/S0140-6736(24)00472-0.
PMID:38614487
Hereditary xanthinuria is not so rare disorder of purine metabolism.
Sebesta I, Stiburkova B, Krijt J.
Nucleosides Nucleotides Nucleic Acids. 2018;37(6):324-328. doi: 10.1080/15257770.2018.1460478. Epub 2018 May 3.
PMID:29723117
Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.
Ichida K, Amaya Y, Okamoto K, Nishino T.
Int J Mol Sci. 2012 Nov 21;13(11):15475-95. doi: 10.3390/ijms131115475.
PMID:23203137
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
Hereditary xanthinuria and urolithiasis in a domestic shorthair cat.
Furman E, Hooijberg EH, Leidinger E, Zedinger C, Giger U, Leidinger J.
Comp Clin Path. 2015 Nov 1;24(6):1325-1329. doi: 10.1007/s00580-015-2072-5. Epub 2015 Jan 30.
PMID:26478726
[Hereditary xanthinuria and molybdenum cofactor deficiency].
Ichida K.
Nihon Rinsho. 2003 Jan;61 Suppl 1:377-82.
PMID:12629751
Management of urinary stones by experts in stone disease (ESD 2025).
Papatsoris A, Geavlete B, Radavoi GD, Alameedee M, Almusafer M, Ather MH, Budia A, Cumpanas AA, Kiremi MC, Dellis A, Elhowairis M, Galán-Llopis JA, Geavlete P, Guimerà Garcia J, Isern B, Jinga V, Lopez JM, Mainez JA, Mitsogiannis I, Mora Christian J, Moussa M, Multescu R, Oguz Acar Y, Petkova K, Piñero A, Popov E, Ramos Cebrian M, Rascu S, Siener R, Sountoulides P, Stamatelou K, Syed J, Trinchieri A.
Arch Ital Urol Androl. 2025 Jun 30;97(2):14085. doi: 10.4081/aiua.2025.14085. Epub 2025 Jun 30.
PMID:40583613
Modern diagnostic approach to hereditary xanthinuria.
Mraz M, Hurba O, Bartl J, Dolezel Z, Marinaki A, Fairbanks L, Stiburkova B.
Urolithiasis. 2015 Feb;43(1):61-7. doi: 10.1007/s00240-014-0734-4. Epub 2014 Nov 6.
PMID:25370766
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