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Decoding blood ecosystem to promote precision prevention and management of human diseasesCheng, TZhōnghuá xuèyèxué zázhì, 2021-01, Vol.42 (1), p.1ChinaTexto completo disponível |
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Abnormal hemoglobinopathy in Hb Titusville: a case reportZheng, Y F ; Zhang, L JZhōnghuá xuèyèxué zázhì, 2023-12, Vol.44 (12), p.1051-1051ChinaTexto completo disponível |
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The correlation between rheumatic immunopathy and lymphomaYang, C M ; Fang, M YZhōnghuá xuèyèxué zázhì, 2019-10, Vol.40 (10), p.880ChinaTexto completo disponível |
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Reflections on the innovative research and development of hematologic oncology drugs under the new situationTang, L ; Chen, X M ; Zou, L M ; Du, Y ; Qi, Y L ; Yang, Z MZhōnghuá xuèyèxué zázhì, 2021-12, Vol.42 (12), p.969-973ChinaTexto completo disponível |
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A case of recurrent acute promyelocytic leukemia with p.R394G resistanceShi, Y ; Yao, J J ; Yao, Y H ; Liu, Z B ; Gao, F ; Li, X Y ; Feng, S QZhōnghuá xuèyèxué zázhì, 2023-12, Vol.44 (12), p.1049-1050ChinaTexto completo disponível |
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Material Type: Artigo
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Hemophagocytic syndrome with elevated alpha-fetoprotein: 3 cases report and literature reviewLiu, Y M ; Zhang, W ; Cao, Q Y ; Xie, X Y ; Li, L J ; Fu, R ; Shao, Z H ; Song, JZhōnghuá xuèyèxué zázhì, 2023-12, Vol.44 (12), p.1038-1040ChinaTexto completo disponível |
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Material Type: Artigo
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Clinical characteristics of 34 adult patients with acute leukemias of ambiguous lineagePei, C X ; Zhan, Q ; Liu, C N ; Peng, W ; Wang, L ; Liu, L ; Li, Y J ; Liao, Y ; Luo, X HZhōnghuá xuèyèxué zázhì, 2023-11, Vol.44 (11), p.940-944ChinaTexto completo disponível |
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Material Type: Artigo
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Clinical characteristics and gene mutation analysis of two families with hereditary protein C deficiencyZeng, M L ; Yang, L L ; Zou, A Q ; Chen, Y ; Jia, K Q ; Wang, M S ; Jin, Y HZhōnghuá xuèyèxué zázhì, 2023-11, Vol.44 (11), p.952-955ChinaTexto completo disponível |
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Material Type: Artigo
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Clinical features of hemophagocytic lymphohistiocytosis associated with myeloid neoplasms: a report of 8 casesLi, Y Q ; Zhang, Y H ; Teng, G S ; Hu, N B ; Wang, Y ; Duan, Y F ; Bai, JZhōnghuá xuèyèxué zázhì, 2023-11, Vol.44 (11), p.949-951ChinaTexto completo disponível |
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Material Type: Artigo
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A family with hereditary FⅪ deficiency caused by compound heterozygous mutationZheng, X Y ; Jin, Y H ; Xu, Y Y ; Yang, L L ; Zhu, L Q ; Wang, H H ; Jiang, S T ; Wang, M SZhōnghuá xuèyèxué zázhì, 2021-08, Vol.42 (8), p.687-689ChinaTexto completo disponível |