Hasil Pencarian - Xuandi Li

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  1. 1
    Treatment Option for Abernethy Malformation—Two Cases Report and Review of the Literature

    Treatment Option for Abernethy Malformation—Two Cases Report and Review of the Literature oleh Yuese Lin, Yuese Lin, Xuandi Li, Xuandi Li, Shujuan Li, Shujuan Li, Hongjun Ba, Hongjun Ba, Huishen Wang, Huishen Wang, Ling Zhu, Ling Zhu

    Diterbitkan 2020-10-01
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  2. 2
    Stent implantation in severe aortic coarctation in a pediatric patient with Turner syndrome: Case report and literature review

    Stent implantation in severe aortic coarctation in a pediatric patient with Turner syndrome: Case report and literature review oleh Yuese Lin, Yuese Lin, Ling Zhu, Ling Zhu, Xuandi Li, Xuandi Li, Hongjun Ba, Hongjun Ba, Xiufang He, Xiufang He, Shujuan Li, Shujuan Li

    Diterbitkan 2023-01-01
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  3. 3
    Amiodarone-Related Pure Red Cell Aplastic Anemia and Hypothyroidism in a Child With Total Anomalous Pulmonary Venous Connection

    Amiodarone-Related Pure Red Cell Aplastic Anemia and Hypothyroidism in a Child With Total Anomalous Pulmonary Venous Connection oleh Hongjun Ba, Lingling Xu, Huimin Peng, Xuandi Li, Yuese Lin, Huishen Wang, Youzhen Qin

    Diterbitkan 2019-09-01
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  4. 4
    Chronic Active Epstein-Barr Virus Infection With Systemic Vasculitis and Pulmonary Arterial Hypertension in a Child

    Chronic Active Epstein-Barr Virus Infection With Systemic Vasculitis and Pulmonary Arterial Hypertension in a Child oleh Hongjun Ba, Lingling Xu, Huimin Peng, Yuese Lin, Xuandi Li, Huishen Wang, Youzhen Qin

    Diterbitkan 2019-06-01
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  5. 5
    Beta Blocker Therapy for Congenital Hepatic Arteriovenous Fistula in Two Neonates

    Beta Blocker Therapy for Congenital Hepatic Arteriovenous Fistula in Two Neonates oleh Hongjun Ba, Lingling Xu, Huimin Peng, Yuese Lin, Xuandi Li, Youzhen Qin, Huishen Wang

    Diterbitkan 2020-04-01
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  6. 6
    Haploinsufficiency of A20 in a Chinese child caused by loss-of-function mutations in TNFAIP3: A case report and review of the literature

    Haploinsufficiency of A20 in a Chinese child caused by loss-of-function mutations in TNFAIP3: A case report and review of the literature oleh Jing Liu, Jing Liu, Yuese Lin, Yuese Lin, Xuandi Li, Xuandi Li, Hongjun Ba, Hongjun Ba, Xiufang He, Xiufang He, Huimin Peng, Huimin Peng, Shujuan Li, Shujuan Li, Ling Zhu, Ling Zhu

    Diterbitkan 2023-01-01
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  7. 7
    Duchenne Muscular Dystrophy With Low Acidic α-Glucosidase Activity: Two Case Reports and Literature Review

    Duchenne Muscular Dystrophy With Low Acidic α-Glucosidase Activity: Two Case Reports and Literature Review oleh Xiufang He, Xiufang He, Xuandi Li, Xuandi Li, Yuese Lin, Yuese Lin, Hongjun Ba, Hongjun Ba, Huimin Peng, Huimin Peng, Lili Zhang, Lili Zhang, Ling Zhu, Ling Zhu, Youzhen Qin, Youzhen Qin, Shujuan Li, Shujuan Li

    Diterbitkan 2022-06-01
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  8. 8
    Sitosterolemia With Atherosclerosis in a Child: A Case Report

    Sitosterolemia With Atherosclerosis in a Child: A Case Report oleh Hongjun Ba, Hongjun Ba, Huimin Peng, Xiufang He, Liangping Cheng, Yuese Lin, Xuandi Li, Huishen Wang, Youzhen Qin, Youzhen Qin

    Diterbitkan 2021-06-01
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  9. 9
    Identification of Hub Biomarkers and Immune and Inflammation Pathways Contributing to Kawasaki Disease Progression with RT-qPCR Verification

    Identification of Hub Biomarkers and Immune and Inflammation Pathways Contributing to Kawasaki Disease Progression with RT-qPCR Verification oleh Hongjun Ba, Lili Zhang, Huimin Peng, Xiufang He, Yuese Lin, Xuandi Li, Shujuan Li, Ling Zhu, Youzhen Qin, Xing Zhang, Yao Wang

    Diterbitkan 2023-01-01
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  10. 10
    Case Report: Talaromyces marneffei Infection in a Chinese Child With a Complex Heterozygous CARD9 Mutation

    Case Report: Talaromyces marneffei Infection in a Chinese Child With a Complex Heterozygous CARD9 Mutation oleh Hongjun Ba, Hongjun Ba, Huimin Peng, Liangping Cheng, Yuese Lin, Xuandi Li, Xiufang He, Shujuan Li, Huishen Wang, Youzhen Qin, Youzhen Qin

    Diterbitkan 2021-06-01
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