Art

J-GLOBAL ID：201702218119746274   Reference number：17A0359641

Livedoid vasculopathy and popliteal artery occlusion in a patient with protein S deficiency

蛋白質S欠損患者におけるリベド血管症と膝窩動脈閉鎖

Author (7)： Nakayama Takayuki (Department of Transfusion Medicine, Aichi Medical University, Nagakute, Japan) ,  Mizutani Kentaro (Department of Dermatology, Aichi Medical University, Nagakute, Japan) ,  Hanamura Ichiro (Department of Hematology, Aichi Medical University, Nagakute, Japan) ,  Kato Hidefumi (Department of Transfusion Medicine, Aichi Medical University, Nagakute, Japan) ,  Takami Akiyoshi (Department of Hematology, Aichi Medical University, Nagakute, Japan) ,  Takeshita Kyosuke (Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan) ,  Watanabe Daisuke (Department of Dermatology, Aichi Medical University, Nagakute, Japan)
Material： Journal of Dermatology  (J Dermatol)
Volume： 44  Issue： 2  Page： 198-201  Publication year： Feb. 2017 
JST Material Number： W1578A  ISSN： 0385-2407  Document type： Article
Article type： 原著論文  Country of issue： Australia (AUS)  Language： ENGLISH (EN)

Thesaurus term： *blood coagulation disorder ,...
Semi thesaurus term： *Protein S Deficiency ,...

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Author keywords (5)： congenital thrombophilia ,  livedoid vasculopathy ,  protein C pathway ,  protein S deficiency ,  protein S Tokushima

JST classification (3)： Clinical dermatology in general  (GF01030J) ,  Clinical medicine on cardiovascular system in general  (GJ01030V) ,  Biological function  (EB03040U)

Substance index (2)： Aspirin ,  Warfarin potassium

Reference (15)：

• Acland KM, Darvay A, Wakelin SH, Russell-Jones R. Livedoid vasculitis: a manifestation of the antiphospholipid syndrome? Br J Dermatol 1999; 140 (1): 131-135.
• Khenifer S, Thomas L, Balme B, Dalle S. Livedoid vasculiltis associated with a double heterozygous Factor V Leiden and prothrombin G20210A gene mutations. Clin Exp Dermatol 2009; 34 (8): e811-e813.
• Criado PR, Rivitti EA, Sotto MN, de Carvalho JF. Livedoid vasculopathy as a coagulation disorder. Autoimmun Rev 2011; 10 (6): 353-360.
• Tatewaki H, Iida H, Nakahara M et al. A novel splice acceptor site mutation which produces multiple splicing abnormalities resulting in protein S deficiency type I. Thromb Haemost 1999; 82 (1): 65-71.
• Hayashi T, Nishioka J, Shigekiyo T, Saito S, Suzuki K. Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S. Blood 1994; 83 (3): 683-690.

Terms in the title (6)： 蛋白質S ,  欠損 ,  患者 ,  リベド血管症 ,  膝窩動脈 ,  閉鎖