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Primary hyperoxaluria.

作者信息

Rumsby Gill, Cochat Pierre

出版信息

N Engl J Med. 2013 Nov 28;369(22):2163. doi: 10.1056/NEJMc1311606.

DOI:10.1056/NEJMc1311606
PMID:24283239
Abstract
摘要

相似文献

1
Primary hyperoxaluria.原发性高草酸尿症
N Engl J Med. 2013 Nov 28;369(22):2163. doi: 10.1056/NEJMc1311606.
2
Complexity of pre-emptive liver transplantation in children with primary hyperoxaluria type 1.1型原发性高草酸尿症患儿进行先发制肝移植的复杂性
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Reversal by liver transplantation of the complications of primary hyperoxaluria as well as the metabolic defect.肝移植对原发性高草酸尿症并发症及代谢缺陷的逆转作用。
N Engl J Med. 1989 Oct 19;321(16):1100-3. doi: 10.1056/NEJM198910193211607.
4
Multidisciplinary Cooperation in a Simultaneous Combined Liver and Kidney Transplantation Patient of Primary Hyperoxaluria 1.原发性高草酸尿症1型肝肾联合移植患者的多学科合作
JNMA J Nepal Med Assoc. 2017 Jan-Mar;56(205):175-178.
5
Combined liver-kidney transplantation in primary hyperoxaluria type 1.1型原发性高草酸尿症的肝肾联合移植
Transplantation. 1990 Nov;50(5):886-7.
6
Transplantation in primary hyperoxaluria type 1.1型原发性高草酸尿症的移植治疗
Nephrol Dial Transplant. 1995;10(8):1293-6.
7
Combined liver-kidney transplantation. For the genetic disorder primary hyperoxaluria type I.肝肾联合移植。用于治疗遗传性疾病I型原发性高草酸尿症。
Mt Sinai J Med. 1994 Jan;61(1):32-6.
8
Primary hyperoxaluria type I.I型原发性高草酸尿症
Australas Radiol. 1994 Nov;38(4):345.
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Primary hyperoxaluria.原发性高草酸尿症。
N Engl J Med. 2013 Nov 28;369(22):2162-3. doi: 10.1056/NEJMc1311606.
10
Combined auxiliary split liver and kidney transplantation for type I primary hyperoxaluria and end-stage kidney disease.联合辅助性劈离肝肾移植治疗I型原发性高草酸尿症和终末期肾病。
Nephrology (Carlton). 2014 Dec;19(12):814-5. doi: 10.1111/nep.12325.

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Lumasiran at birth changes the trajectory of primary hyperoxaluria type 1: same disease, different outcomes in two affected siblings.出生时使用鲁马西兰改变了1型原发性高草酸尿症的病程:两名患病兄弟姐妹患同一种疾病,却有不同结局。
J Nephrol. 2025 Jul 9. doi: 10.1007/s40620-025-02325-2.
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Population Pharmacokinetic and Pharmacodynamic Modelling and Simulation for Nedosiran Clinical Development and Dose Guidance in Pediatric Patients with Primary Hyperoxaluria Type 1.用于1型原发性高草酸尿症儿科患者奈多司坦临床开发和剂量指导的群体药代动力学和药效学建模与模拟
Clin Pharmacokinet. 2025 Jul 2. doi: 10.1007/s40262-025-01540-1.
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Primary hyperoxaluria type I diagnosed after a kidney transplant presenting with subcutaneous calcification: a case report of sodium thiosulfate treatment.
肾移植后诊断为I型原发性高草酸尿症并伴有皮下钙化:硫代硫酸钠治疗的病例报告
Front Pharmacol. 2025 May 13;16:1485024. doi: 10.3389/fphar.2025.1485024. eCollection 2025.
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Primary Hyperoxaluria Screening and Monitoring: Quantitative Measurement of Plasma Oxalate by Gas Chromatography-Mass Spectrometry With High Sensitivity.原发性高草酸尿症的筛查和监测:采用高灵敏度气相色谱-质谱法对血浆草酸盐进行定量检测。
Ann Lab Med. 2024 May 1;44(3):235-244. doi: 10.3343/alm.2023.0178. Epub 2023 Oct 31.
5
Granulomatous Inflammation and Hypercalcemia in Patients With Severe Systemic Oxalosis.重症系统性草酸盐中毒患者的肉芽肿性炎症和高钙血症
Kidney Int Rep. 2021 Nov 24;7(2):343-349. doi: 10.1016/j.ekir.2021.11.020. eCollection 2022 Feb.
6
Hyperoxaluria: An early diagnosis will allow a timely combined renal and liver transplantations to avoid irreversible damages to all other organs.高草酸尿症:早期诊断将有助于及时进行肾脏和肝脏联合移植,以避免对所有其他器官造成不可逆转的损害。
J Transl Int Med. 2021 Dec 31;9(4):318-322. doi: 10.2478/jtim-2020-000X. eCollection 2021 Dec 1.
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Dysregulated oxalate metabolism is a driver and therapeutic target in atherosclerosis.草酸代谢失调是动脉粥样硬化的驱动因素和治疗靶点。
Cell Rep. 2021 Jul 27;36(4):109420. doi: 10.1016/j.celrep.2021.109420.
8
Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2.原发性高草酸尿症 3 型与 1 型和 2 型的临床特征比较。
Nephrol Dial Transplant. 2022 Apr 25;37(5):869-875. doi: 10.1093/ndt/gfab027.
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Identification of 8 novel gene variants in primary hyperoxaluria in 21 Chinese children with urinary stones.鉴定 21 例尿路结石的原发性高草酸尿症患儿中的 8 种新基因变异。
World J Urol. 2019 Aug;37(8):1713-1721. doi: 10.1007/s00345-018-2563-5. Epub 2018 Nov 28.
10
Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations.1型原发性高草酸尿症复合杂合子患者的鉴定:临床评估与计算机模拟研究
BMC Nephrol. 2017 Oct 2;18(1):303. doi: 10.1186/s12882-017-0719-y.