Search Results - Wu, Ruo-Hao

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  1. 1
    DNA index as prognostic factor in childhood acute lymphoblastic leukemia in the COG-TARGET database

    DNA index as prognostic factor in childhood acute lymphoblastic leukemia in the COG-TARGET database by Qiu, Kun-yin, Liao, Xiong-yu, He, Zhan-wen, Wu, Ruo-hao, Li, Yang, Xu, Lu-hong, Zhou, Dun-hua, Fang, Jian-pei

    Published in BMC cancer
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  2. 2
    Progressive encephalomyelitis with rigidity and myoclonus: a pediatric case report and literature review

    Progressive encephalomyelitis with rigidity and myoclonus: a pediatric case report and literature review by Li, Yu, Wang, Jing-Wen, Chen, Qi-Hui, Wu, Ruo-Hao, Luo, Xiang-Yang, He, Zhan-Wen

    Published in BMC pediatrics
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  3. 3
    Eltrombopag as first‐line treatment for thrombocytopenia among paediatric patients after allogeneic haematopoietic stem cell transplantation

    Eltrombopag as first‐line treatment for thrombocytopenia among paediatric patients after allogeneic haematopoietic stem cell transplantation by Qiu, Kun‐yin, Liao, Xiong‐yu, Huang, Ke, Wu, Ruo‐hao, Xu, Hong‐gui, Xu, Lu‐hong, Li, Yang, Weng, Wen‐jun, Zhou, Dun‐hua, Fang, Jian‐pei

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  4. 4
    Identification of novel CSNK2A1 variants and the genotype–phenotype relationship in patients with Okur–Chung neurodevelopmental syndrome: a case report and systematic literature review

    Identification of novel CSNK2A1 variants and the genotype–phenotype relationship in patients with Okur–Chung neurodevelopmental syndrome: a case report and systematic literature re... by Wu, Ruo-hao, Tang, Wen-ting, Qiu, Kun-yin, Li, Xiao-juan, Tang, Dan-xia, Meng, Zhe, He, Zhan-wen

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  5. 5
    Atrial septal defect in a patient with congenital disorder of glycosylation type 1a: a case report

    Atrial septal defect in a patient with congenital disorder of glycosylation type 1a: a case report by Wu, Ruo-Hao, Li, Dong-Fang, Tang, Wen-Ting, Qiu, Kun-Yin, Li, Yu, Liao, Xiong-Yu, Tang, Dan-Xia, Qin, Li-Jun, Deng, Bing-Qing, Luo, Xiang-Yang

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  6. 6
    Diagnosis and treatment of juvenile myelomonocytic leukemia

    Diagnosis and treatment of juvenile myelomonocytic leukemia by Liao, Xiong-yu, Qiu, Kun-yin, Fang, Jian-pei, Wu, Ruo-hao, Guo, Shu-yi, Huang, Ke, Zhou, Dun-hua

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  7. 7
    X-linked Hyper-IgM Syndrome: A Phenotype of Crohn's Disease with Hemophagocytic Lymphohistiocytosis

    X-linked Hyper-IgM Syndrome: A Phenotype of Crohn's Disease with Hemophagocytic Lymphohistiocytosis by Qiu, Kun-Yin, Liao, Xiong-Yu, Wu, Ruo-Hao, Huang, Ke, Fang, Jian-Pei, Zhou, Dun-Hua

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  8. 8
    MECP2 duplication syndrome: a clinical analysis of three cases and literature review

    MECP2 duplication syndrome: a clinical analysis of three cases and literature review by Tang, Dan-Xia, Li, Dong-Fang, Wu, Ruo-Hao, Zhang, Li-Na, Luo, Xiang-Yang

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  9. 9
    Identification of novel variants and the genotype–phenotype relationship in patients with Okur–Chung neurodevelopmental syndrome: a case report and systematic literature review

    Identification of novel variants and the genotype–phenotype relationship in patients with Okur–Chung neurodevelopmental syndrome: a case report and systematic literature review by Ruo-hao Wu, Wen-ting Tang, Kun-yin Qiu, Xiao-juan Li, Dan-xia Tang, Zhe Meng, Zhan-wen He

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  10. 10
    X-linked Hyper-IgM Syndrome: A Phenotype of Crohn's Disease with Hemophagocytic Lymphohistiocytosis

    X-linked Hyper-IgM Syndrome: A Phenotype of Crohn's Disease with Hemophagocytic Lymphohistiocytosis by Qiu, Kun-yin, Liao, Xiong-yu, Wu, Ruo-hao, Huang, Ke, Fang, Jian-pei, Zhou, Dun-hua

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  11. 11
    Combined hepatocellular cholangiocarcinoma: Controversies to be addressed

    Combined hepatocellular cholangiocarcinoma: Controversies to be addressed by Wang, An-Qiang, Zheng, Yong-Chang, Du, Juan, Zhu, Cheng-Pei, Huang, Han-Chun, Wang, Shan-Shan, Wu, Liang-Cai, Wan, Xue-Shuai, Zhang, Hao-Hai, Miao, Ruo-Yu, Sang, Xin-Ting, Zhao, Hai-Tao

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  12. 12
    Influencers on Social Media as References: Understanding the Importance of Parasocial Relationships

    Influencers on Social Media as References: Understanding the Importance of Parasocial Relationships by Su, Bo-Chiuan, Wu, Li-Wei, Chang, Yevvon-Yi-Chi, Hong, Ruo-Hao

    Published in Sustainability
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  13. 13
    Phenome-wide investigation of the causal associations between childhood BMI and adult trait outcomes: a two-sample Mendelian randomization study

    Phenome-wide investigation of the causal associations between childhood BMI and adult trait outcomes: a two-sample Mendelian randomization study by Dong, Shan-Shan, Zhang, Kun, Guo, Yan, Ding, Jing-Miao, Rong, Yu, Feng, Jun-Cheng, Yao, Shi, Hao, Ruo-Han, Jiang, Feng, Chen, Jia-Bin, Wu, Hao, Chen, Xiao-Feng, Yang, Tie-Lin

    Published in Genome medicine
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  14. 14
    Epigenetic Element-Based Transcriptome-Wide Association Study Identifies Novel Genes for Bipolar Disorder

    Epigenetic Element-Based Transcriptome-Wide Association Study Identifies Novel Genes for Bipolar Disorder by Yao, Shi, Wu, Hao, Liu, Tong-Tong, Wang, Jia-Hao, Ding, Jing-Miao, Guo, Jing, Rong, Yu, Ke, Xin, Hao, Ruo-Han, Dong, Shan-Shan, Yang, Tie-Lin, Guo, Yan

    Published in Schizophrenia bulletin
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  15. 15
    3例MECP2重复综合征临床分析和文献复习

    3例MECP2重复综合征临床分析和文献复习 by 唐丹霞 李栋方 吴若豪 张丽娜 罗向阳

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