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The Landscape and Horizon: Diagnosis and Treatment of Hereditary Angioedema in China
XU Yingyang, ZHI Yuxiang
2025, 4(3): 283-286. DOI: 10.12376/j.issn.2097-0501.2025.03.001
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Research Progress of Icatibant in the Treatment of Hereditary Angioedema
XU Yanhua, GUO Yinshi
2025, 4(3): 287-293. DOI: 10.12376/j.issn.2097-0501.2025.03.002
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Research Progress in Gene Therapy for Hereditary Angioedema
SHI Yuqi, LIU Juan, ZHI Yuxiang
2025, 4(3): 294-301. DOI: 10.12376/j.issn.2097-0501.2025.03.003
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Research Progress on the Risk of Venous Thromboembolism in Patients with Hereditary Angioedema
JIANG Siqi, ZHI Yuxiang
2025, 4(3): 302-307. DOI: 10.12376/j.issn.2097-0501.2025.03.004
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Distribution Characteristics and Genetic Variation Analysis of Mitochondrial Encephalomyopathy in Children: a Multicenter Study in Hainan Province
DENG Lin, LU Jun, CHEN Xiuling, LI Yuanlong
2025, 4(3): 308-315. DOI: 10.12376/j.issn.2097-0501.2025.03.005
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A Case of Multidisciplinary Treatment for Deficiency of Adenosine Deaminase 2
ZHANG Jingyuan, WU Xiaoqi, DAI Jiayuan, JIN Xianghong, CAO Yuze, LUO Rui, ZHANG Hanlin, DU Tiekuan, CHU Xiaotian, CHEN Peipei, QIAN Hao, YAN Pengguang, XU Jin, SHEN Min
2025, 4(3): 316-324. DOI: 10.12376/j.issn.2097-0501.2025.03.006
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Treatment of Hereditary Angioedema with Lanadelumab: Four Case Reports and Literature Review
ZHANG Wenjing, CAI Liping, LIU Yun, LAI He
2025, 4(3): 325-330. DOI: 10.12376/j.issn.2097-0501.2025.03.007
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A Case of Hereditary Angioedema
QIAO Zusha, WANG Yan, WANG Yanqing, YANG Lu, MA Yan
2025, 4(3): 331-333. DOI: 10.12376/j.issn.2097-0501.2025.03.008
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Chlorhexidine and Fondaparinux-Induced Kounis Syndrome: a Case Report
YU Fangzheng, WANG Yajing, LIN Hang, ZHANG Lifeng, ZHU Yuhui, SHI Xiaomeng, ZHOU Huimin, LIN Nan, GAO Xiang
2025, 4(3): 334-340. DOI: 10.12376/j.issn.2097-0501.2025.03.009
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Post-Orgasmic Illness Syndrome: Two Cases Treated with Autologous Seminal Plasma Subcutaneous Cluster Immunotherapy
LI Lun, DUAN Yanping, ZHI Fan, ZHANG Jing, LI Yu, LIU Bei, YIN Jia
2025, 4(3): 341-347. DOI: 10.12376/j.issn.2097-0501.2025.03.010
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A Case of Neurofibromatosis Type 1 Complicated with Bilateral Sensorineural Hearing Loss
GAO Ruzhen, FAN Xinmiao, GU Wei, YANG Tengyu, ZHANG Zhuhua, WANG Tao, MA Mingsheng, XIA Zenan, FU Hanhui, LIU Yaping, CHEN Xiaowei
2025, 4(3): 348-354. DOI: 10.12376/j.issn.2097-0501.2025.03.011
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A Case Report of Jansen-de Vries Syndrome Caused by PPM1D Gene Mutation and Literature Review
XUE Mei, PANG Bo, ZHANG Xiaoqian, GAO Ziyu, ZHOU Bo, ZHANG Zhixin
2025, 4(3): 355-360. DOI: 10.12376/j.issn.2097-0501.2025.03.012
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Advances in Lipid-Lowering Therapy for Homozygous Familial Hypercholesterolemia
LI Rui, TIAN Zhuang, ZHANG Shuyang
2025, 4(3): 361-369. DOI: 10.12376/j.issn.2097-0501.2025.03.013
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Research Progress on the Pathogenesis, Diagnosis and Treatment of Polygenic Autoinflammatory Diseases
LIU Guishan, SHEN Min
2025, 4(3): 370-376. DOI: 10.12376/j.issn.2097-0501.2025.03.014
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Current Status and Prospects of Gene Therapy for Primary Ciliary Dyskinesia
LU Wanqing, LI Yixuan, HE Miao, TIAN Xinlun, LIU Yaping
2025, 4(3): 377-383. DOI: 10.12376/j.issn.2097-0501.2025.03.015
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Research Progress of Genes Related to Congenital Lipodystrophy
WANG Bobo, LI Xia, ZHENG Ying, LI Youlei
2025, 4(3): 384-390. DOI: 10.12376/j.issn.2097-0501.2025.03.016
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The Treatment Progress of Fabry Disease
ZANG Ruixian, LI Qian, SUN Shuzhen
2025, 4(3): 391-398. DOI: 10.12376/j.issn.2097-0501.2025.03.017
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