Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lauriane Nikuze"'
Publikováno v:
Platelets, Vol 34, Iss 1 (2023)
ANKRD26-related thrombocytopenia (ANKRD26-RT or THC2, MIM 188 000), an autosomal dominant thrombocytopenia, is unresponsive to immunosuppressive therapy and susceptible to hematological malignancies. A large number of pediatric patients are diagnosed
Externí odkaz:
https://doaj.org/article/b3fd691b6996463c9492b5ddb9a39767
Autor:
Zhengjing Lu, Lauriane Nikuze, Zhoulin Zhong, Fang Li, Fuyong Zhang, Kairong Liang, Manlv Wei, Hongying Wei
Publikováno v:
Platelets, Vol 31, Iss 3, Pp 355-359 (2020)
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://doaj.org/article/c68a5802dfc1440c8cd406e4de89ffb0
Autor:
Li-Fang, Huang, Li-Li, Yu, Lauriane, Nikuze, Sanjeev, Singh, Jin-Xia, Jiang, Jia-Li, Jiang, Yu-Ping, Li, Yu-Hui, Qin, Hong-Ying, Wei
Publikováno v:
Hemoglobin. 45:318-321
β-Thalassemia (β-thal), one of the most common form of single-gene inheritable blood diseases in the world, is highly prevalent in southern China, especially in the Guangxi Zhuang Autonomous Region. To update the β-thal mutation spectrum in this r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22edec7fb36767639aa0053e4469c16a
https://doi.org/10.1080/03630269.2022.2041435
https://doi.org/10.1080/03630269.2022.2041435
Publikováno v:
Blood Coagulation & Fibrinolysis
Congenital factor VII deficiency (FVIID) is a rare F7 gene mutation causing bleeding disorder inherited in an autosomal recessive manner. In this study, we aimed to identify genetic defects and analyze their relationships with phenotype in three Chin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::676123c1db52f8d2adc9652112b4f3aa
https://doi.org/10.1097/mbc.0000000000001022
https://doi.org/10.1097/mbc.0000000000001022
Autor:
Jiali Jiang, Junli Zhou, Lauriane Nikuze, Hongying Wei, Manlv Wei, Sanjeev Singh, Yuping Li, Jinxia Jiang, Lifang Huang
Publikováno v:
Scandinavian Journal of Immunology. 95
Wiskott-Aldrich syndrome (WAS) also called the eczema-thrombocytopenia-immunodeficiency syndrome is a primary immunodeficiency disease with X-linked recessive inheritance caused by mutations in the WAS protein (WASp) gene and characterized by thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf3754ad8c000630997b3545453880bc
https://doi.org/10.1111/sji.13115
https://doi.org/10.1111/sji.13115
Autor:
Kairong Liang, Fang Li, Manlv Wei, Zhoulin Zhong, Fuyong Zhang, Zhengjing Lu, Lauriane Nikuze, Hongying Wei
Publikováno v:
Platelets. 31:355-359
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c3bcb05622237f58043f5cd6fd3eb9
https://doi.org/10.1080/09537104.2019.1615614
https://doi.org/10.1080/09537104.2019.1615614
Autor:
Zhengjing, Lu, Lauriane, Nikuze, Zhoulin, Zhong, Fang, Li, Fuyong, Zhang, Kairong, Liang, Manlv, Wei, Hongying, Wei
Publikováno v:
Platelets. 31(3)
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex. We analyzed the expression of GPIIb/IIIa and the gene sequencing in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8c746dbd3bb5d509c562593608726ae
https://pubmed.ncbi.nlm.nih.gov/31088191
https://pubmed.ncbi.nlm.nih.gov/31088191
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