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  1. Article

    Open Access

    Identification of leukocyte-lymphocyte ratio as a novel prognostic factor in Peripheral T-cell lymphoma

    Peripheral T-cell lymphoma (PTCL) is notorious for its heterogeneity as well as poor prognosis. High mortality remains a challenge. Our study aims to assess whether the leukocyte-lymphocyte ratio (LLR) and neu...

    Shi-Qi Gao, Bo-Ya Lei, Yue Xu, Zi-Jian Zhang in Holistic Integrative Oncology (2023)

  2. No Access

    Article

    Ophthalmic characteristics and retinal vasculature changes in Williams syndrome, and its association with systemic diseases

    We aim to characterise the ophthalmic findings and retinal vasculature changes in patients with WS, and to analyse the correlation between ophthalmic manifestations and the associated systemic diseases.

    Tsai-Chu Yeh, Hui-Chen Cheng, Hsing-Yuan Li, Sheng Chu Chi, Hsin-Yu Yang in Eye (2023)

  3. No Access

    Article

    Associations of SGLT2 genetic polymorphisms with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults

    Sodium-glucose cotransporter 2 (SGLT2) inhibitors lowers blood pressure (BP) and exert a salutary effect on the salt sensitivity of BP. This study aimed to examine the associations of SGLT2 genetic variants with ...

    Hao Jia, Peng Bao, Shi Yao, ** Zhang, Jian-Jun Mu, Gui-Lin Hu in Hypertension Research (2023)

  4. Article

    Open Access

    Sex differences in impact of cumulative systolic blood pressure from childhood to adulthood on albuminuria in midlife: a 30-year prospective cohort study

    Albuminuria is recognized as being a predictor of cardiovascular and renal disease. We aimed to identify the impact of the long-term burden and trends of systolic blood pressure on albuminuria in midlife, as w...

    Dan Wang, Pu-qing Kou, Yue-yuan Liao, Ke-ke Wang, Yu Yan, Chen Chen in BMC Public Health (2023)

  5. No Access

    Article

    Combined metabolomics and machine learning algorithms to explore metabolic biomarkers for diagnosis of acute myocardial ischemia

    Acute myocardial ischemia (AMI) remains the leading cause of death worldwide, and the post-mortem diagnosis of AMI represents a current challenge for both clinical and forensic pathologists. In the present stu...

    Jie Cao, Jian Li, Zhen Gu, Jia-jia Niu in International Journal of Legal Medicine (2023)

  6. No Access

    Article

    Salt-inducible kinase 1-CREB-regulated transcription coactivator 1 signalling in the paraventricular nucleus of the hypothalamus plays a role in depression by regulating the hypothalamic–pituitary–adrenal axis

    Elucidating the molecular mechanism underlying the hyperactivity of the hypothalamic–pituitary–adrenal axis during chronic stress is critical for understanding depression and treating depression. The secretion...

    Yuan Wang, Ling Liu, Jiang-Hong Gu, Cheng-Niu Wang, Wei Guan in Molecular Psychiatry (2022)

  7. Article

    Open Access

    Author Correction: Development and clinical deployment of a smartphone-based visual field deep learning system for glaucoma detection

    Fei Li, Di** Song, Han Chen, Jian **ong, **ngyi Li, Hua Zhong in npj Digital Medicine (2022)

  8. Article

    Open Access

    Hearing characteristics of infantile-onset Pompe disease after early enzyme-replacement therapy

    Studies suggest that enzyme-replacement therapy (ERT) is crucial to the survival of patients with infantile-onset Pompe disease (IOPD). Hearing impairment (HI) is one of the clinical sequelae observed in long-...

    Chien-Yu Hsueh, Chii-Yuan Huang, Chia-Feng Yang in Orphanet Journal of Rare Diseases (2021)

  9. Article

    Open Access

    Audiological and otologic manifestations of glutaric aciduria type I

    Glutaric aciduria type 1 (GA-1) is a rare disease connected with speech delay and neurological deficits. However, the audiological and otologic profiles of GA-1 have not yet been fully characterized. To our kn...

    Yen-Chi Chen, Chii-Yuan Huang, Yen-Ting Lee in Orphanet Journal of Rare Diseases (2020)

  10. Article

    Open Access

    Development and clinical deployment of a smartphone-based visual field deep learning system for glaucoma detection

    By 2040, ~100 million people will have glaucoma. To date, there are a lack of high-efficiency glaucoma diagnostic tools based on visual fields (VFs). Herein, we develop and evaluate the performance of ‘iGlauco...

    Fei Li, Di** Song, Han Chen, Jian **ong, **ngyi Li, Hua Zhong in npj Digital Medicine (2020)

  11. Article

    Exploring an Integrative Therapy for Treating COVID-19: A Randomized Controlled Trial

    To develop a new Chinese medicine (CM)-based drug and to evaluate its safety and effect for suppressing acute respiratory distress syndrome (ARDS) in COVID-19 patients.

    Jia-bo Wang, Zhong-xia Wang, **g **g in Chinese Journal of Integrative Medicine (2020)

  12. No Access

    Article

    S100A14 suppresses metastasis of nasopharyngeal carcinoma by inhibition of NF-kB signaling through degradation of IRAK1

    Nasopharyngeal carcinoma (NPC) is a unique head and neck cancer with highly aggressive and metastatic potential in which distant metastasis is the main reason for treatment failure. Till present, the underlyin...

    Dong-Fang Meng, Rui Sun, Guo-Ying Liu, Li-**a Peng, Li-Sheng Zheng, ** **e in Oncogene (2020)

  13. No Access

    Article

    Coronary CT Angiography Using Low Iodine Delivery Rate and Tube Voltage Determined by Body Mass Index: Superiority in Clinical Practice

    To explore the feasibility and superiority of iodine delivery rate (IDR) and tube voltage determined by patients’ body mass index (BMI) in coronary CT angiography (CCTA), a total of 1567 patients undertaking C...

    Wang Yuan, Ting-ting Qu, Hui-juan Wang, Mei-yu Wang, Yuan Qu in Current Medical Science (2019)

  14. No Access

    Article

    Signal Alteration of Substantia Nigra on 3.0T Susceptibility-weighted Imaging in Parkinson’s Disease and Vascular Parkinsonism

    Recent researches have found that 7 Tesla SWI can detect the alteration of substantia nigra hyperintensity in Parkinson’s disease (PD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). ...

    Xue-jun Zhao, **-yuan Niu, He-yang You, Min Zhou, Xue-bing Ji in Current Medical Science (2019)

  15. No Access

    Article

    Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched case-control study

    To examine the association of genetic variants with characteristic symptoms of type 2 diabetes mellitus (T2DM).

    Hao-ying Dou, Yuan-yuan Wang, Nan Yang in Chinese Journal of Integrative Medicine (2017)

  16. Article

    Open Access

    Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA

    Mucopolysaccharidosis IVA (MPS IVA) is a rare lysosomal storage disorder caused by N-acetylgalactosamine-6-sulfatase deficiency, which catalyzes a step in the catabolism of glycosaminoglycans, keratan sulfate and...

    Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen in Orphanet Journal of Rare Diseases (2014)