المؤلفون: Pang, Congfei, Wu, Xiaomei, Nikuze, Lauriane, Wei, Hongying

المساهمون: National Natural Science Foundation of China

المصدر: Platelets ; volume 34, issue 1 ; ISSN 0953-7104 1369-1635

الإتاحة: https://doi.org/10.1080/09537104.2023.2262607Test

المؤلفون: Congfei Pang, Xiaomei Wu, Nikuze, Lauriane, Hongying Wei

المصدر: Platelets; Dec2023, Vol. 34 Issue 1, p1-7, 7p

مصطلحات موضوعية: TREATMENT effectiveness, MEAN platelet volume, THROMBOCYTOPENIA, CHILD patients, HEMATOLOGIC malignancies

الشركة/الكيان: WORLD Health Organization

المؤلفون: Liang, Kairong, Nikuze, Lauriane, Zhang, Fuyong, Lu, Zhengjing, Wei, Manlv, Wei, Hongying

المصدر: Blood Coagulation & Fibrinolysis ; volume 32, issue 5, page 340-343 ; ISSN 0957-5235 1473-5733

الإتاحة: https://doi.org/10.1097/mbc.0000000000001022Test

المؤلفون: Jiang, Jiali, Zhou, Junli, Wei, Manlv, Singh, Sanjeev, Nikuze, Lauriane, Huang, Lifang, Li, Yuping, Jiang, Jinxia, Wei, Hongying

المصدر: Scandinavian Journal of Immunology ; volume 95, issue 1 ; ISSN 0300-9475 1365-3083

الإتاحة: https://doi.org/10.1111/sji.13115Test

المؤلفون: Huang, Li-Fang, Yu, Li-Li, Nikuze, Lauriane, Singh, Sanjeev, Jiang, Jin-Xia, Jiang, Jia-Li, Li, Yu-Ping, Qin, Yu-Hui, Wei, Hong-Ying

المصدر: Hemoglobin ; volume 45, issue 5, page 318-321 ; ISSN 0363-0269 1532-432X

الإتاحة: https://doi.org/10.1080/03630269.2022.2041435Test

المؤلفون: Meirong Lu, Ning Liao, Yonghong Lei, Siyuan Jia, Hongying Wei, Yunyan He, Kairong Liang, Nikuze Lauriane

المصدر: Gene. 702:143-147

مصطلحات موضوعية: Adult, Blood Platelets, Male, 0301 basic medicine, Proband, Mutant, Mutation, Missense, Gene mutation, Biology, Frameshift mutation, 03 medical and health sciences, Exon, 0302 clinical medicine, Genetics, medicine, Humans, Missense mutation, Factor XIII deficiency, Child, Aged, Sequence Deletion, Factor XIII, Blood Proteins, General Medicine, Middle Aged, medicine.disease, Factor XIII Deficiency, Pedigree, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c02620526ae5c0462d0d9a3b8691bf9Test
https://doi.org/10.1016/j.gene.2019.03.067Test

المؤلفون: Jiang, Jiali, Zhou, Junli, Wei, Manlv, Singh, Sanjeev, Nikuze, Lauriane, Huang, Lifang, Li, Yuping, Jiang, Jinxia, Wei, Hongying

المصدر: Scandinavian Journal of Immunology; Jan2022, Vol. 95 Issue 1, p1-8, 8p

مصطلحات موضوعية: WISKOTT-Aldrich syndrome, PRIMARY immunodeficiency diseases, AGAMMAGLOBULINEMIA, FRAMESHIFT mutation, ECZEMA, FLOW cytometry

المؤلفون: Lu, Zhengjing, Nikuze, Lauriane, Zhong, Zhoulin, Li, Fang, Zhang, Fuyong, Liang, Kairong, Wei, Manlv, Wei, Hongying

المساهمون: Natural Science Foundation of Guangxi Province

المصدر: Platelets ; volume 31, issue 3, page 355-359 ; ISSN 0953-7104 1369-1635

الإتاحة: https://doi.org/10.1080/09537104.2019.1615614Test

المؤلفون: Kairong Liang, Nikuze, Lauriane, Fuyong Zhang, Zhengjing Lu, Manlv Wei, Hongying Wei

المصدر: Blood Coagulation & Fibrinolysis; Jul2021, Vol. 32 Issue 5, p340-343, 4p

المؤلفون: Lu, Zhengjing¹ (AUTHOR), Nikuze, Lauriane¹ (AUTHOR), Zhong, Zhoulin² (AUTHOR), Li, Fang³ (AUTHOR), Zhang, Fuyong⁴ (AUTHOR), Liang, Kairong¹ (AUTHOR), Wei, Manlv¹ (AUTHOR), Wei, Hongying¹ (AUTHOR) whylhr@qq.com

المصدر: Platelets. 2020, Vol. 31 Issue 3, p355-359. 5p.

مصطلحات موضوعية: *BLOOD platelet aggregation, *GENEALOGY, *BLOOD platelets, *GENOTYPES, *IDENTIFICATION