Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis-Reference-Cited by-同舟云学术

Molecular pathogenesis of plasminogen Hakodate: the second Japanese family case of severe type I plasminogen deficiency manifested late-onset multi-organic chronic pseudomembranous mucositis

Published:2016-05-19 Issue:2 Volume:42 Page:218-224
ISSN:0929-5305
Container-title:Journal of Thrombosis and Thrombolysis
language:en
Short-container-title:J Thromb Thrombolysis

Author:

Osaki Tsukasa,Souri Masayoshi,Song Young-seok,Izumi Naohiro,Law Ruby,Ichinose Akitada

Funder

Yamagata University

the Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT)

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Hematology

Link

http://link.springer.com/content/pdf/10.1007/s11239-016-1375-y.pdf

Reference17 articles.

1. Schuster V, Hügle B, Tefs K (2007) Plasminogen deficiency. J Thromb Haemost 5:2315–2322

2. Tefs K, Gueorguieva M, Klammt J et al (2006) Molecular and clinical spectrum of type I plasminogen deficiency: a series of 50 patients. Blood 108:3021–3026

3. Klammt J, Kobelt L, Aktas D et al (2011) Identification of three novel plasminogen (PLG) gene mutations in a series of 23 patients with low PLG activity. Thromb Haemost 105:454–460

4. Ooe A, Kida M, Yamazaki T et al (1999) Common mutation of plasminogen detected in three Asian populations by an amplification refractory mutation system and rapid automated capillary electrophoresis. Thromb Haemost 82:1342–1346

5. Suzuki T, Ikewaki J, Iwata H et al (2009) The first two Japanese cases of severe type I congenital plasminogen deficiency with ligneous conjunctivitis: successful treatment with direct thrombin inhibitor and fresh plasma. Am J Hematol 84:363–365

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