Výsledky vyhledávání

Research on Influencing Factors of Satisfaction with the Use of Public Health Internet Platform: Evidence from Ding Xiang Doctor (DXY) Internet Medical Platform

Autor: Yanlong Guo, Lan Zu, Denghang Chen, Han Zhang

Publikováno v: International Journal of Environmental Research and Public Health
Volume 20
Issue 3
Pages: 2276

With the rapid development of Internet information technology, Internet medical platforms are gradually entering daily life. Especially after the outbreak of the COVID-19 pandemic, it becomes very difficult for patients to go out for medical treatmen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d207fc6f33bbd11f45b1d2aebb6f5dea

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A Study of Public Attitudes toward Shanghai’s Image under the Influence of COVID-19: Evidence from Comments on Sina Weibo

Autor: Yanlong Guo, Lan Zu, Denghang Chen, Han Zhang

Publikováno v: International Journal of Environmental Research and Public Health
Volume 20
Issue 3
Pages: 2297

With the advent of the Internet era, Chinese users tend to choose to express their opinions on social media platforms represented by Sina Weibo. The changes in people’s emotions toward cities from the microblogging texts can reflect the image of ci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b8b0efafc9cc93ed4e5c4f5a956a1d8

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Akademický článek

System for Measuring and Protecting the Anode Current of TH2103A Klystron

Autor: Yali CHEN, Bo LU, Xingyu BAI, Yuexin MA, Lingfei XU, Jun LIANG, Lan ZUO

Publikováno v: 南方能源建设, Vol 11, Iss 3, Pp 146-151 (2024)

[Introduction] The 3.7 GHz high-power TH2103A klystrons are widely used in the tokamak experimental device. To simplify the HV power supply system (removing the vacuum tetrode in the anode modulation), a power supply mode based on voltage division mo

Externí odkaz: https://doaj.org/article/cde882dec80d472991b89ac9ec410a38

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Rippling muscle disease: Evidence for phenotypic and genetic heterogeneity

Autor: Lan Zu, Karla P. Figueroa, Carlos Barraza, Yuen T. So, Stefan M. Pulst

Publikováno v: Muscle & Nerve. 24:340-344

We describe the clinical features of a family with rippling muscle disease. Muscle stiffness and myalgia were the most prominent symptoms. Muscle rippling, although distinctive, was present in only 6 of the 11 affected family members, whereas persist

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f8fdc63ae344afb8aa49c0ee5c6d54a3
https://doi.org/10.1002/1097-4598(200103)24:3<340::aid-mus1003>3.0.co

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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10

Autor: Madhureeta Achari, David L. Nelson, Lan Zu, Mehrdad Khajavi, Astrid Rasmussen, Kei Watase, Alanna E. McCall, Takanori Yamagata, Daniel L. Burgess, Huda Y. Zoghbi, Elisa Alonso, Tohru Matsuura, Jeffrey L. Noebels, Stefan M. Pulst, Raji P. Grewal, Caleb F. Davis, T. Ashizawa

Publikováno v: Nature Genetics. 26:191-194

Spinocerebellar ataxia type 10 (SCA10; MIM 603516; refs 1,2) is an autosomal dominant disorder characterized by cerebellar ataxia and seizures. The gene SCA10 maps to a 3.8-cM interval on human chromosome 22q13-qter (refs 1,2). Because several other

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b67fbc7bd54d0d679031303d501eef
https://doi.org/10.1038/79911

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Akademický článek

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Bethlem myopathy in a black creole pedigree

Autor: Lan Zu, Michael C. Graves, Thomas L. Anderson, Cameron R. Adams, Carlos A. Garcia, Karla P. Figueroa, Stefan M. Pulst

Publikováno v: Journal of clinical neuromuscular disease. 4(1)

OBJECTIVES: To analyze the clinical and molecular features of a distinctive muscular dystrophy in a family of black Creole descent. METHODS: We clinically characterized a four-generation pedigree and performed linkage analysis for all relevant autoso

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25f0bd4bcc9b1381a5036d02f71c59f0
https://pubmed.ncbi.nlm.nih.gov/19078680

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Akademický článek

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Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22

Autor: Lan Zu, Karla P. Figueroa, Stefan M. Pulst, Raji P. Grewal

SummaryThe autosomal dominant cerebellar ataxias (ADCAs) are a clinically and genetically heterogeneous group of disorders. The clinical symptoms include cerebellar dysfunction and associated signs from dysfunction in other parts of the nervous syste

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c573444173200bb0b0d9a044442a6ddb
https://europepmc.org/articles/PMC1377770/

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