Evaluation Of Factor V Leiden, Prothrombin Mutations and The Homozygous mutation 677T In The MTHFR Gene In Patients With Venous Thrombosis

被引:0
|
作者
Pizzuti, Michele
Santagostino, Alberto
Rizzo, Maria Antonietta
Dragonetti, Daniela
Pietrafesa, Maria Grazia
Attolico, Immacolata
Amendola, Angela
Filardi, Nunzio
Cimminiello, Michele
Matturro, Angela
Vertone, Domenico
Nuccorini, Roberta
Pascale, Sara Pasquina
Coluzzi, Sabrina
机构
关键词
D O I
10.1182/blood.V122.21.4798.4798
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
4798
引用
收藏
页数:1
相关论文
共 50 条
  • [41] Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations
    Nazli Dilay Gultekin
    Fatma Hilal Yilmaz
    Huseyin Tokgoz
    Nuriye Tarakci
    Umran Caliskan
    Indian Pediatrics, 2019, 56 : 143 - 144
  • [42] Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations
    Gultekin, Nazli Dilay
    Yilmaz, Fatma Hilal
    Tokgoz, Huseyin
    Tarakci, Nuriye
    Caliskan, Umran
    INDIAN PEDIATRICS, 2019, 56 (02) : 143 - 144
  • [43] Risk of venous thrombosis in individuals possesing factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations.
    Donnelly, JG
    Isotalo, PA
    CLINICAL CHEMISTRY, 2000, 46 (06) : A205 - A205
  • [44] Prevalence of the factor V Leiden mutation and the MTHFR C677T mutation in thrombophilic and in healthy persons
    Gaustadnes, M
    Larsen, TB
    Ingerslev, J
    Petersen, BN
    Madsen, M
    Bihl, K
    Rudiger, N
    THROMBOSIS AND HAEMOSTASIS, 1997, : P2324 - P2324
  • [45] Prothrombin G20210A mutation, and not factor V Leiden mutation, is a risk factor for cerebral venous thrombosis in Brazilian patients.
    Rodrigues, CA
    Rocha, LKA
    Morelli, VM
    Noguti, MAE
    Silveira, RC
    De Leon, CMP
    Lourenco, DM
    BLOOD, 2003, 102 (11) : 109B - 109B
  • [46] Factor V Leiden mutation among patients with venous thrombosis in India
    Srivastava, A
    Shaji, RV
    Muralitharan, S
    Reuben, YK
    Dennison, D
    Chandy, M
    THROMBOSIS AND HAEMOSTASIS, 1997, : PS908 - PS908
  • [47] The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis
    H. G. Koch
    P. Nabel
    R. Junker
    K. Auberger
    R. Schobess
    A. Homberger
    M. Linnebank
    U. Nowak-Göttl
    European Journal of Pediatrics, 1999, 158 : S113 - S116
  • [48] Combined severe factor XII deficiency and homozygous factor V Leiden mutation in a patient with venous thrombosis
    Miljic, P
    Colovic, M
    Boskovic, D
    Rakicevic, L
    Djordjevic, V
    THROMBOSIS RESEARCH, 2002, 106 (4-5) : 265 - 267
  • [49] FACTOR-V LEIDEN MUTATION AND VENOUS THROMBOSIS
    OZSOYLU, S
    LANCET, 1995, 345 (8942): : 133 - 133
  • [50] Factor V Leiden mutation as a cause of venous thrombosis
    Lobato-Salinas, Z
    Cambra-Lasaosa, FJ
    Campistol, J
    Toll-Costa, T
    Pons-Odena, M
    Palomeque-Rico, A
    Martín, JM
    REVISTA DE NEUROLOGIA, 2004, 38 (02) : 136 - 139