Zobrazeno 1 - 10
of 333
pro vyhledávání: '"FXII gene"'
Autor:
Haiyue Zhang1 (AUTHOR), Siqi Liu1 (AUTHOR), Chanchan Lin1 (AUTHOR), Shasha Luo1 (AUTHOR), Lihong Yang1 (AUTHOR), Yanhui Jin1 (AUTHOR), Liqing Zhu1 (AUTHOR), Mingshan Wang1 (AUTHOR)
Publikováno v:
Hematology. 2019, Vol. 24 Issue 1, p420-425. 6p. 2 Diagrams, 3 Charts.
Autor:
Zhang, Haiyue1 (AUTHOR), Liu, Siqi1 (AUTHOR), Lin, Chanchan1 (AUTHOR), Luo, Shasha1 (AUTHOR), Yang, Lihong1 (AUTHOR), Jin, Yanhui1 (AUTHOR), Zhu, Liqing1 (AUTHOR), Wang, Mingshan1 (AUTHOR) wywms@126.com
Publikováno v:
Hematology. Dec2019, Vol. 24 Issue 1, p420-425. 6p.
Publikováno v:
Revista Portuguesa de Medicina Geral e Familiar, Vol 40, Iss 2 (2024)
Hereditary angioedema (HAE) is a rare, hereditary disease and its manifestations may be life-threatening. It differs from histaminergic angioedema since it shows different underlying mechanisms and, therefore, does not respond to antihistamine or adr
Externí odkaz:
https://doaj.org/article/70bfc5b591624d0bb6b9787a8c40cc42
Autor:
Lihong Yang, Haiyue Zhang, Chanchan Lin, Liqing Zhu, Shasha Luo, Yanhui Jin, Siqi Liu, Mingshan Wang
Publikováno v:
Hematology (Amsterdam, Netherlands). 24(1)
To study the gene mutation of human coagulation factor XII (FXII) in a Chinese family with FXII deficiency and it will help us to understand the pathogenesis of this type of disease.The proband was a 50-year-old male who had a fracture of the right h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919db88ccd81eaf7483243a00a4b4849
https://pubmed.ncbi.nlm.nih.gov/30929639
https://pubmed.ncbi.nlm.nih.gov/30929639
Akademický článek
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Autor:
Peter Hoffmann, Elisabete Cordeiro, Thomas Renné, João Bosco Pesquero, Christiane Stieber, Sandra Barth, Sven Cichon, Anete Sevciovic Grumach, M. M. Nöthen, Rosemeire Navickas Constantino-Silva
Publikováno v:
British Journal of Dermatology. 173:1102-1104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ade600876216cfe6773f7e0922b52e95
https://doi.org/10.1111/bjd.13791
https://doi.org/10.1111/bjd.13791
Autor:
Stieber, Christiane, Veronez, Camila, Cagini, Nathalia, Cordeiro, Elisabete, Grumach, Anete S., Constantino-Silva, Rosemeire, Pesquero, Joao Bosco, Cichon, Sven
Publikováno v:
In The Journal of Allergy and Clinical Immunology February 2014 133(2) Supplement:AB31-AB31
Autor:
Sven Cichon, Camila Lopes Veronez, Nathália Cagini, Christiane Stieber, Anete Sevciovic Grumach, Elisabete Cordeiro, Rosemeire Navickas Constantino-Silva, João Bosco Pesquero
Publikováno v:
Journal of Allergy and Clinical Immunology. 133:AB31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a60550f05427a9406034839ca12e4bdf
https://doi.org/10.1016/j.jaci.2013.12.139
https://doi.org/10.1016/j.jaci.2013.12.139
Autor:
Liu, Meina1 (AUTHOR), Wang, Huanhuan1 (AUTHOR), Lin, Miaomiao1 (AUTHOR), Jin, Yanhui1 (AUTHOR), Yang, Lihong1 (AUTHOR), Wang, Mingshan1 (AUTHOR) wywms@126.com
Publikováno v:
Hematology. Dec2020, Vol. 25 Issue 1, p502-506. 5p.
Autor:
Xu, Fei1 (AUTHOR), Qin, Langyi1 (AUTHOR), Zou, Anqing1 (AUTHOR), Hou, Lingling1 (AUTHOR), Wang, Mingshan1 (AUTHOR), Chen, Bile2 (AUTHOR) zjwzcbl@126.com
Publikováno v:
Orphanet Journal of Rare Diseases. 10/9/2024, Vol. 19 Issue 1, p1-8. 8p.