THROMBOEMBOLIC EVENTS AFTER RADICAL PROSTATECTOMY IN PATIENTS WITH HEREDITARY THROMBOPHILIA DUE TO FACTOR V LEIDEN

被引：0
作者：
Knipper, Sophie
Ekrutt, Jonas
Tennstedt, Pierre
Heinzer, Hans
Tilki, Derya
Graefen, Markus
机构：
来源：
JOURNAL OF UROLOGY | 2020年 / 203卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
MP74-12
引用
收藏
页码：E1136 / E1136
页数：1
相关论文
共 50 条
  • [41] Factor V Leiden mutation and other thrombophilia markers in childhood ischemic stroke
    Duran, R
    Biner, B
    Demir, M
    Çeltik, C
    Karasalihoglu, S
    [J]. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 2005, 11 (01) : 83 - 88
  • [42] Factor V Leiden - the commonest molecular defect in arterial and venous thrombophilia in India
    Ahmed, RPH
    Gupta, PK
    Kannan, M
    Choudhry, VP
    Saxena, R
    [J]. THROMBOSIS RESEARCH, 2003, 110 (01) : 19 - 21
  • [43] Homozygous Factor V Leiden Thrombophilia in a Patient With Histologically Confirmed Thromboangiitis Obliterans
    Mensa, Mussa
    Dobbs, Tom
    Jessop, Zita M.
    Whitaker, Iain S.
    [J]. CLINICAL MEDICINE INSIGHTS-CASE REPORTS, 2019, 12
  • [44] Coexistence of hereditary homocystinuria and Factor V Leiden - Effect on thrombosis
    Mandel, H
    Brenner, B
    Berant, M
    Rosenberg, N
    Lanir, N
    Jakobs, C
    Fowler, B
    Seligsohn, U
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (12) : 763 - 768
  • [45] The incidence of Factor V Leiden in fetal thrombotic events
    Longtine, J
    Roberts, DJ
    [J]. LABORATORY INVESTIGATION, 1997, 76 (01) : 2 - 2
  • [46] FAMILIAL THROMBOPHILIA (FACTOR V LEIDEN HETEROZYGOSITY, HIGH FACTOR VIII) IN WOMEN WITH "IDIOPATHIC" OSTEONECROSIS
    Richardson-Royer, C. M.
    Hadid, A.
    Richardson-Royer, C. M.
    Glueck, C. J.
    Wang, P.
    [J]. JOURNAL OF INVESTIGATIVE MEDICINE, 2014, 62 (04) : 709 - 709
  • [47] Polygenic thrombophilia: Factor II gene variation and factor V Leiden mutation in a French family
    Conard, J
    MabileauBrouzes, C
    Horellou, MH
    Elalamy, I
    Samama, MM
    [J]. PRESSE MEDICALE, 1997, 26 (20): : 951 - 953
  • [48] High prevalence of protein C, protein S, antithrombin deficiency, and Factor V Leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident
    Ali, Nadir
    Ayyub, Muhammad
    Khan, Saleem Ahmed
    [J]. PAKISTAN JOURNAL OF MEDICAL SCIENCES, 2014, 30 (06) : 1323 - 1326
  • [49] Ocular Vascular Thrombotic Events: A Diagnostic Window to Familial Thrombophilia (Compound Factor V Leiden and Prothrombin Gene Heterozygosity) and Thrombosis
    Glueck, Charles J.
    Wang, Ping
    [J]. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 2009, 15 (01) : 12 - 18
  • [50] Factor V Leiden related risk of thromboembolic and bleeding complications in patients with established coronary heart disease
    Mahmoodi, B. K.
    Bergmeijer, T.
    Vos, G.
    Kelder, J.
    Deneer, V.
    Hackeng, C.
    Ten Berg, J.
    [J]. EUROPEAN HEART JOURNAL, 2017, 38 : 382 - 383
12345