| [1] |
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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| [2] |
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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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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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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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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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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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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| [8] |
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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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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| [10] |
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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Hu Yuhan, Chen Fei.
Diagnostic value of ultrasound with serology and BRAF testing in the identification of benign and malignant TI-RADS category 4 nodules
[J]. Clinical Focus, 2022, 37(4): 339-342.
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| [12] |
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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| [13] |
Zhao Wanqing, Zhang Yanan, Wei Chenxi, Bai Xinli.
Methylmalonic acidemia: clinical phenotype and genetic characteristics
[J]. Clinical Focus, 2022, 37(2): 145-149.
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| [14] |
Cui Qingyang, Wang Mengbin, Cao Yinli, Tang Chenghe.
A case report and literature review on severe combined immunodeficiency caused by new mutation of RAG1 gene
[J]. Clinical Focus, 2022, 37(2): 155-161.
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| [15] |
Wang Pengrui, Chen Huaqian, Yang Tao, Zhao Li, Li Peng.
The effect of serum intact parathyroid hormone level on the maturation of autogeneous arteriovenous fistula
[J]. Clinical Focus, 2022, 37(12): 1094-1098.
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