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Profil bibliographique

Kun Hu

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

29Publications signalées
108Citations signalées
3Affiliations récentes

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Les domaines associés

Diabetes Treatment and ManagementTraditional Chinese Medicine StudiesAcute Ischemic Stroke ManagementCannabis and Cannabinoid ResearchIntracranial Aneurysms: Treatment and Complications

Les publications récentes

Accès ouvert 2025 article OpenAlex

Electrocoagulation therapy for a patient with an acute thalamoperforating artery pseudoaneurysm: a case report

Xiaoping Zhou, Guanlin Huang, Mingang Zou, Kun Hu et autres

BACKGROUND: Thalamoperforating artery (TPA) pseudoaneurysms are relatively uncommon and often pose significant challenges in detection through vascular examination. Furthermore, their management, particularly via endovascular therapy, is complex and demanding. This article presents a case study of a patient diagnosed with an acute …

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2 citations BMC Cardiovascular Disorders
2025 article OpenAlex

Exploring the medication rules of national TCM master WANG Qi in treating bronchial asthma based on data mining

Han MA, Kun Hu, Ji Wang

目的 挖掘王琦院士治疗支气管哮喘的用药规律,拓宽治疗支气管哮喘的临床诊疗思路,为中医治疗支气管哮喘提供临床依据和参考。 方法 采集并整理王琦院士门诊治疗支气管哮喘的完整医案,使用Excel 2019建立治疗支气管哮喘的方药数据库,运用SPSS Modeler 18.0、SPSS Statistics 26.0、Gephi 0.10.1软件进行频次统计、关联规则、聚类分析及数据可视化,然后运用中医学理论对统计结果进行分析讨论。 结果 纳入治疗支气管哮喘的处方546首,涉及中药195味,总用药频次为6564次。常用中药为乌梅、蝉蜕、灵芝、甘草、苦杏仁等,以解表药、清热药和补虚药为主,药性以平为主,药味多甘辛苦,归经多属肺经、肝经、脾经。挖掘得到关联规则20条(2味药14条、3味药6条),包括“防风-乌梅”“石膏-乌梅”“麻黄-乌梅”“苦杏仁-乌梅”等。聚类分析得到5类药物,包括“乌梅、蝉蜕、灵芝、防风”“麻黄、石膏、苦杏仁、甘草”等多种药物组合。主成分因子分析共提取出6个公因子,包括“麻黄、苦杏仁、石膏、甘草”“乌梅、蝉蜕、灵芝”等。 结论 王琦院士临证辨治支气管哮喘重视“调体抗过敏和宣肺泄热平喘”相结合,强调解表药与清热药的配合应用,提出“辨体-辨病-辨证”相结合辨治支气管哮喘的新思路。

0 citations Lishizhen Medicine and Materia Medica Research
Accès ouvert 2025 article OpenAlex

Sodium valproate, a potential repurposed treatment for the neurodegeneration in Wolfram syndrome (TREATWOLFRAM): trial protocol for a pivotal multicentre, randomised double-blind controlled trial

Renuka Dias, Kristian Brock, Kun Hu, Rajat Gupta et autres

Introduction Wolfram syndrome ( WFS1- Spectrum Disorder) is an ultra-rare monogenic form of progressive neurodegeneration and diabetes mellitus. In common with most rare diseases, there are no therapies to slow or stop disease progression. Sodium valproate, an anticonvulsant with neuroprotective properties, is …

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7 citations BMJ Open
Accès ouvert 2021 article OpenAlex

WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome

Kun Hu, Malgorzata Zatyka, Dewi Astuti, Nicola L. Beer et autres

Background Wolfram syndrome (WFS) is a rare disorder characterised by childhood-onset diabetes mellitus and progressive optic atrophy. Most patients have variants in the WFS1 gene. We undertook functional studies of WFS1 variants and correlated these with WFS1 protein expression and phenotype. Methods …

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30 citations Journal of Medical Genetics

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