| [1] |
Liu Wanqi, Fan Shuqin, Zhuang Ruixue, He Feng, Liu Zhenchuan, Xie Zhongxiang.
Intracranial infection of varicella zoster virus in adults: Clinical analysis of 5 cases
[J]. Clinical Focus, 2024, 39(2): 149-154.
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| [2] |
Lv Shasha, Song Jinlan, Shi Jian.
Mitochondrial mutation m.3243A> G associated with diabetes mellitus: One case report and literature review
[J]. Clinical Focus, 2024, 39(2): 160-163.
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| [3] |
Liu Lili, Yuan Yuting, Lai Gengliang, Tian Chuan, Lan Xiang, Ye Zhonglv.
The relationship between minimal residual disease on day 15 and prognosis in children with acute lymphoblastic leukemia
[J]. Clinical Focus, 2024, 39(1): 47-52.
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| [4] |
Zhao Xin, Liu Yun.
Generative artificial intelligence: Ethical review on the empowerment in medical humanities education
[J]. Clinical Focus, 2024, 39(1): 65-69.
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| [5] |
Dong Zhengrong, Tao Qianshan, Shen Yuanyuan, Dong Yi.
Analysis of the follow-up results of 163 patients with acute promyelocytic leukemia
[J]. Clinical Focus, 2023, 38(9): 813-818.
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| [6] |
Xie Xinrong, Gan Jinghua, Qin Rui, Zhong Muxian.
Androgen insensitivity syndrome combined with choriocarcinoma and human chorionic gonadotropin-induced hyperthyroidism: A case and literature review
[J]. Clinical Focus, 2023, 38(7): 628-632.
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| [7] |
Wolazihan Madeniyati, Dilixiati Tuerdimaimaiti, Li Mengchen, Baihetinisha Tuerdi.
Meta-analysis of the application value of metagenomic next-generation sequencing technology in the diagnosis of pulmonary tuberculosis
[J]. Clinical Focus, 2023, 38(5): 389-398.
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| [8] |
Zhao Shuzhen, Wang Sanping, Zhao Xiaoyun.
SLC32A1 gene mutation in hereditary epilepsy with febrile convulsion addition: A case report and literature review
[J]. Clinical Focus, 2023, 38(5): 451-454.
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| [9] |
Du Jiayi, Liu Lili, He Yongzhong, Tian Chuan, Lan Xiang, Ye Zhonglyu.
Clinical observation of serious adverse events in children with acute lymphoblastic leukemia during chemotherapy
[J]. Clinical Focus, 2023, 38(2): 149-154.
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| [10] |
Pang Shu, Zhang Mingkai, Bai Hongmei, Wu Yongdong.
Congenital insensitivity to pain with anhidrosis: A case report and literature review
[J]. Clinical Focus, 2023, 38(1): 64-67.
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| [11] |
Liu Yuqing, Cheng Ji.
Familial Holt-Oram syndrome: Report of a case & literature review
[J]. Clinical Focus, 2023, 38(1): 71-74.
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| [12] |
Zhang Yueyue, Xie Meifang, Sun Gen.
Rheumatoid arthritis complicated with T-cell large granular lymphocytic leukemia: A case report and literature review
[J]. Clinical Focus, 2022, 37(8): 728-732.
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| [13] |
Peng Yu, Jiang Zhihong, Wang Zhihai.
Clinical and genetic analysis of a neonate with congenital central nervous system multiple malformation: An identification on mutations in VANGL1 genes
[J]. Clinical Focus, 2022, 37(7): 640-643.
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| [14] |
Ma Cuixia, Feng Lulu, Li Lixin, Ma Qianqian, Li Yang, Feng Jizhen.
Analysis on de novo mutations in PAH genes of the family with phenylalanine hydroxylase deficiency
[J]. Clinical Focus, 2022, 37(5): 441-446.
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| [15] |
Liu Debin, Chen Xiaopu, Chen Wenjie, Huang Yinting, He Wenzhen.
Relations between aspirin & clopidogrel resistance-relatedgene polymorphisms and corresponding recurrent cerebral infarction
[J]. Clinical Focus, 2022, 37(4): 320-324.
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