[1] |
Michael M, Bagga A, Sartain SE, et al. Haemolytic uraemic syndrome[J]. Lancet, 2022, 400(10364): 1722-1740. doi: 10.1016/S0140-6736(22)01202-8.
|
[2] |
Sarno L, Conca P, Capuano A, et al. A Life-Threating Postpartum Atypical Hemolytic-Uremic Syndrome with Multiorgan Involvement[J]. J Clin Med, 2022, 11(23):6957. doi: 10.3390/jcm11236957.
|
[3] |
Bruel A, Kavanagh D, Noris M, et al. Hemolytic Uremic Syndrome in Pregnancy and Postpartum[J]. Clin J Am Soc Nephrol, 2017, 12(8):1237-1247. doi: 10.2215/CJN.00280117.
|
[4] |
Jokiranta TS. HUS and atypical HUS[J]. Blood, 2017, 129(21):2847-2856. doi: 10.1182/blood-2016-11-709865.
pmid: 28416508
|
[5] |
Aigner C, Schmidt A, Gaggl M, et al. An updated classification of thrombotic microangiopathies and treatment of complement gene variant-mediated thrombotic microangiopathy[J]. Clin Kidney J, 2019, 12(3):333-337. doi: 10.1093/ckj/sfz040.
pmid: 31198225
|
[6] |
Fakhouri F, Schwotzer N, Frémeaux-Bacchi V. How I diagnose and treat atypical hemolytic uremic syndrome[J]. Blood, 2023, 141(9):984-995. doi: 10.1182/blood.2022017860.
|
[7] |
Scully M, Neave L. Etiology and outcomes: Thrombotic microangiopathies in pregnancy[J]. Res Pract Thromb Haemost, 2023, 7(2):100084. doi: 10.1016/j.rpth.2023.100084.
|
[8] |
Leisring J, Brodsky SV, Parikh SV. Clinical Evaluation and Management of Thrombotic Microangiopathy[J]. Arthritis Rheumatol, 2024, 76(2):153-165. doi: 10.1002/art.42681.
|
[9] |
Zheng XL, Vesely SK, Cataland SR, et al. ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura[J]. J Thromb Haemost, 2020, 18(10):2486-2495. doi: 10.1111/jth.15006.
|
[10] |
Giannubilo SR, Marzioni D, Tossetta G, et al. HELLP Syndrome and Differential Diagnosis with Other Thrombotic Microangiopathies in Pregnancy[J]. Diagnostics(Basel), 2024, 14(4):352. doi: 10.3390/ diagnostics14040352.
|
[11] |
Timmermans S, Werion A, Spaanderman M, et al. The natural course of pregnancies in women with primary atypical haemolytic uraemic syndrome and asymptomatic relatives[J]. Br J Haematol, 2020, 190(3):442-449. doi: 10.1111/bjh.16626.
|
[12] |
血液净化急诊临床应用专家共识组. 血液净化急诊临床应用专家共识[J]. 中华急诊医学杂志, 2017, 36(1):24-36. doi: 10.3760/ cma.j.issn.1671-0282.2017.01.007.
|
[13] |
Kato H, Nangaku M, Hataya H, et al. Clinical guides for atypical hemolytic uremic syndrome in Japan[J]. Clin Exp Nephrol, 2016, 20(4):536-543. doi: 10.1007/s10157-016-1276-6.
pmid: 27422619
|
[14] |
Cheong HI, Jo SK, Yoon SS, et al. Clinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in Korea[J]. J Korean Med Sci, 2016, 31(10):1516-1528. doi: 10.3346/jkms.2016.31.10.1516.
pmid: 27550478
|
[15] |
张振宇, 刘惠娜, 袁文静. 产后溶血性尿毒症综合征12例临床分析[J]. 实用妇产科杂志, 2021, 37(6):471-474.
|
[16] |
杨红英, 冯烨, 李东言, 等. 产后溶血性尿毒综合征1例[J]. 中华围产医学杂志, 2024, 27(4):322-327. doi: 10.3760/cma.j.cn113903-20240218-00108.
|
[17] |
国家慢性肾病临床医学研究中心, 中国医师协会肾脏内科医师分会, 中国急性肾损伤临床实践指南专家组. 中国急性肾损伤临床实践指南[J]. 中华医学杂志, 2023, 103(42):3332-3366. doi: 10.3760/cma.j.cn112137-20230802-00133.
|
[18] |
Sciascia S, Yazdany J, Dall′Era M, et al. Anticoagulation in patients with concomitant lupus nephritis and thrombotic microangiopathy: a multicentre cohort study[J]. Ann Rheum Dis, 2019, 78(7):1004-1006. doi: 10.1136/annrheumdis-2018-214559.
pmid: 30552172
|
[19] |
Fremeaux-Bacchi V, Fakhouri F, Garnier A, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults[J]. Clin J Am Soc Nephrol, 2013, 8(4):554-562. doi: 10.2215/CJN.04760512.
|
[20] |
Amari Chinchilla K, Vijayan M, Taveras Garcia B, et al. Complement-Mediated Disorders in Pregnancy[J]. Adv Chronic Kidney Dis, 2020, 27(2):155-164. doi: 10.1053/j.ackd.2020.01.002.
|
[21] |
Ávila A, Cao M, Espinosa M, et al. Recommendations for the individualised management of atypical hemolytic uremic syndrome in adults[J]. Front Med(Lausanne), 2023,10:1264310. doi: 10.3389/fmed.2023.1264310.
|