Attitudes about genetic testing for thrombophilia in a large family with heritable protein C deficiency

被引：0
|
作者：
van Korlaar, I [1 ]
Vossen, C [1 ]
Rosendaal, F [1 ]
Bovill, E [1 ]
Naud, S [1 ]
Cameron, L [1 ]
Kaptein, A [1 ]
机构：
[1] Leiden Univ, Med Ctr, Unit Psychol, Leiden, Netherlands
来源：
PSYCHOLOGY & HEALTH | 2005年 / 20卷
关键词：
D O I：
暂无
中图分类号：
R1 [预防医学、卫生学];
学科分类号：
1004 ; 120402 ;
摘要：
引用
下载
收藏
页码：276 / 277
页数：2
相关论文
共 50 条
  • [1] Attitudes toward genetic testing for thrombophilia in asymptomatic members of a large family with heritable protein C deficiency
    Van Korlaar, IM
    Vossen, CY
    Rosendaal, FR
    Bovill, EG
    Naud, S
    Cameron, LD
    Kaptein, AA
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (11) : 2437 - 2444
  • [2] Molecular genetic analysis in patients with inherited thrombophilia and antithrombin, protein C or protein S deficiency
    Pavlova, A
    Lim-Eimer, M
    Watzka, A
    Lindhoff-Last, E
    Luxembourg, B
    Kreuz, W
    Rusicke, E
    Seifried, E
    Oldenburg, J
    34th Hemophilia Symposium, 2005, : 298 - 301
  • [3] Sagittal sinus thrombosis in a patient with familial Protein C deficiency: Highlighting the impact of thrombophilia testing
    Ab Rahman, Wan Suriana Wan
    Abdullah, Wan Zaidah
    Hassan, Mohd Nazri
    Ahmed, Suhair
    Zulkafli, Zefarina
    Ahmed, Wan Aireene Wan
    Iberahim, Salfarina
    Noor, Noor Haslina Mohd
    MALAYSIAN JOURNAL OF PATHOLOGY, 2021, 43 (03) : 449 - 452
  • [4] PROTEIN-S DEFICIENCY IN A LARGE FAMILY WITH THROMBOPHILIA PREVIOUSLY CHARACTERIZED AS HAVING AN INHERITED FIBRINOLYTIC DEFECT
    ZOLLER, B
    DAHLBACK, B
    THROMBOSIS AND HAEMOSTASIS, 1993, 69 (06) : 1256 - 1256
  • [5] Quantitative trait locus for protein C in a family with thrombophilia
    Tanck, Michael W. T.
    Wichers, Iris M.
    Meijers, Joost C. M.
    Buller, Harry R.
    Reitsma, Pieter H.
    Middeldorp, Saskia
    THROMBOSIS AND HAEMOSTASIS, 2011, 105 (01) : 199 - 201
  • [6] Prenatal genetic testing for familial severe congenital protein C deficiency
    Shinya Tairaku
    Mariko Taniguchi-Ikeda
    Yoko Okazaki
    Yoriko Noguchi
    Yuji Nakamachi
    Takeshi Mori
    Ikuko Kubokawa
    Akira Hayakawa
    Akio Shibata
    Tomomi Emoto
    Hiroki Kurahashi
    Tatsushi Toda
    Seiji Kawano
    Hideto Yamada
    Ichiro Morioka
    Kazumoto Iijima
    Human Genome Variation, 2 (1)
  • [7] Diagnostic challenge of the newborn patients with heritable protein C deficiency
    Masako Ichiyama
    Hirosuke Inoue
    Masayuki Ochiai
    Masataka Ishimura
    Akira Shiraishi
    Junko Fujiyoshi
    Hironori Yamashita
    Kazuo Sato
    Shinya Matsumoto
    Taeko Hotta
    Takeshi Uchiumi
    Dongchon Kang
    Shouichi Ohga
    Journal of Perinatology, 2019, 39 : 212 - 219
  • [8] Diagnostic challenge of the newborn patients with heritable protein C deficiency
    Ichiyama, Masako
    Inoue, Hirosuke
    Ochiai, Masayuki
    Ishimura, Masataka
    Shiraishi, Akira
    Fujiyoshi, Junko
    Yamashita, Hironori
    Sato, Kazuo
    Matsumoto, Shinya
    Hotta, Taeko
    Uchiumi, Takeshi
    Kang, Dongchon
    Ohga, Shouichi
    JOURNAL OF PERINATOLOGY, 2019, 39 (02) : 212 - 219
  • [9] Cascade genetic testing in a large family
    不详
    MEDICAL JOURNAL OF AUSTRALIA, 1996, 164 (08) : 474 - 474
  • [10] Exclusion of heritable protein c and protein S deficiency in patients with an elevated INR
    Szkotak, A. J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 : 381 - 381
12345