布加综合征患者中因子V和亚甲基四氢叶酸还原酶突变的复合杂合性 - Suppr | 超能文献

Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome.

作者信息

Otrock Zaher K, Sharara Ala I, Mahfouz Rami A R, Taher Ali T

出版信息

J Gastroenterol Hepatol. 2006 Apr;21(4):782-3. doi: 10.1111/j.1440-1746.2006.04248.x.

DOI:10.1111/j.1440-1746.2006.04248.x

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome.布加综合征患者中因子V和亚甲基四氢叶酸还原酶突变的复合杂合性

J Gastroenterol Hepatol. 2006 Apr;21(4):782-3. doi: 10.1111/j.1440-1746.2006.04248.x.

2

Budd-Chiari syndrome related to factor V Leiden mutation.与凝血因子V莱顿突变相关的布加综合征

Am J Gastroenterol. 1998 Apr;93(4):651-2. doi: 10.1111/j.1572-0241.1998.184_b.x.

3

Budd-Chiari syndrome associated with factor V leiden mutation: a report of 6 patients.与凝血因子V莱顿突变相关的布加综合征：6例报告

Liver Transpl Surg. 1999 Mar;5(2):96-100. doi: 10.1002/lt.500050211.

4

JAK2V617F mutation as a marker of a latent myeloproliferative disorder in a patient with Budd-Chiari syndrome and factor V Leiden mutation.JAK2V617F突变作为布加综合征合并因子V莱顿突变患者潜在骨髓增殖性疾病的标志物。

Thromb Haemost. 2007 Sep;98(3):681-2.

5

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.布加综合征合并潜在的纯合子因子V莱顿突变和杂合子亚甲基四氢叶酸还原酶突变。

J Gastroenterol. 2005 Oct;40(10):1002-3. doi: 10.1007/s00535-005-1664-2.

6

Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.一名同时携带因子V莱顿突变和凝血酶原基因G20210A突变的杂合子患者发生布加综合征。

Thromb Haemost. 1999 Oct;82(4):1366-7.

7

Acute Budd-Chiari syndrome treated by liver transplantation in a woman homozygous for factor V Leiden.一名因因子V莱顿纯合子导致急性布加综合征的女性接受肝移植治疗。

Eur J Gastroenterol Hepatol. 1996 Sep;8(9):925-7.

8

The relationship between the levels and function of endothelial progenitor cells and factor V Leiden and protein C deficiency in patients with primary Budd-Chiari syndrome.原发性布加综合征患者内皮祖细胞水平及其功能与因子 V 莱顿和蛋白 C 缺乏的关系。

Eur Rev Med Pharmacol Sci. 2018 May;22(9):2742-2750. doi: 10.26355/eurrev_201805_14971.

9

Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.一名患有布加综合征的儿童存在因子V莱顿突变和凝血酶原G20210A突变的复合杂合性。

Eur J Pediatr. 2001 Mar;160(3):198. doi: 10.1007/pl00008425.

10

Coexistence of left-sided inferior vena cava, deep vein thrombosis of the upper and lower extremities and prothrombotic polymorphisms in a young patient: a case report.一名年轻患者左侧下腔静脉并存、上下肢深静脉血栓形成及血栓前多态性：病例报告

Blood Coagul Fibrinolysis. 2008 Jul;19(5):443-5. doi: 10.1097/MBC.0b013e3282f9ae35.