Splenectomy and emerging novel treatments in rare inherited hemolytic anemias.
作者信息
Yacobovich Joanne, Tamary Hannah
机构信息
Hematology Oncology Division, Hematology Unit, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
出版信息
Hemasphere. 2019 Jun 30;3(Suppl). doi: 10.1097/HS9.0000000000000190. eCollection 2019 Jun.
Abstract
摘要
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Blood. 2018 May 17;131(20):2183-2192. doi: 10.1182/blood-2017-10-810796. Epub 2018 Mar 16.
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Recommendations regarding splenectomy in hereditary hemolytic anemias.遗传性溶血性贫血脾切除术的推荐意见。
Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26.
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Senicapoc: a potent candidate for the treatment of a subset of hereditary xerocytosis caused by mutations in the Gardos channel.司尼卡波：一种治疗由加尔杜斯通道突变引起的遗传性口形红细胞增多症亚型的有力候选药物。
Haematologica. 2016 Nov;101(11):e431-e435. doi: 10.3324/haematol.2016.149104. Epub 2016 Jul 21.
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Safe and Efficient Gene Therapy for Pyruvate Kinase Deficiency.丙酮酸激酶缺乏症的安全有效基因治疗
Mol Ther. 2016 Aug;24(7):1187-98. doi: 10.1038/mt.2016.87. Epub 2016 May 3.
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OPSI threat in hematological patients.血液学患者中的暴发性感染性休克威胁
Transl Med UniSa. 2013 May 6;6:2-10. eCollection 2013.
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Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker senicapoc (ICA-17043).镰状细胞病患者的溶血和红细胞生存指标的改善与急性血管阻塞性危象无关：Gardos 通道阻滞剂 senicapoc（ICA-17043）的 III 期随机、安慰剂对照、双盲研究。
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