Výsledky vyhledávání

Cystic fibrosis: Experience in one institution

Autor: Szu-Hung Chu, Chieh-Han Cheng, Chia-Yi Lo, Ling-Chun Liu, Wei Te Lei, Shyh-Dar Shyur, Li-Ching Fang, Li-Hsin Huang, Chen-Kuan Chen, Yu-Hsuan Kao

Publikováno v: Journal of Microbiology, Immunology and Infection. 47(4):358-361

Cystic fibrosis (CF) is one of the most common autosomal recessive inherited disorders among Caucasians. Comparatively, it is considered to be a rare disease among Asians. To date, only a few cases of Taiwanese CF have been published. We report four

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bf0cae57009eb49785237180c816211

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[A Project to Improve the Time-Effectiveness of Routine Morning Blood Tests]

Autor: Chia-Yi, Lo, Lun-Hui, Ho, Yung-Han, Ho, Yu-Li, Lin, Chi-Hung, Liu, Tien-Hui, Wu

Publikováno v: Hu li za zhi The journal of nursing. 62(5)

Morning blood sampling, conducted around 4am to 5am, is routinely ordered due to nothing-by-mouth (NPO) requirements and clinical practice norms. However, this routine may interrupt the normal sleep of patients and decrease the satisfaction of patien

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b899471518e4651be573d5017fc3b46a
https://pubmed.ncbi.nlm.nih.gov/26507630

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Type I hereditary angioedema in Taiwan -- clinical, biological features and genetic study

Autor: Wei-Te, Lei, Shyh-Dar, Shyur, Li-Hsin, Huang, Yu-Hsuan, Kao, Chia-Yi, Lo

Publikováno v: Asian Pacific journal of allergy and immunology. 29(4)

Hereditary angioedema (HAE) is a rare, autosomal dominant inherited disease which is caused by a genetic deficiency of C1 esterase inhibitor (C1 INH). There have only been a few case reports in Taiwan to date.To describe the clinical features of type

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::350feb582cb6ca60928db3f60207cb3e
https://pubmed.ncbi.nlm.nih.gov/22299312

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Clinical manifestations and BTK gene defect in 4 unrelated Taiwanese families with Bruton's disease

Autor: Kuo-Hsi, Lee, Shyh-Dar, Shyur, Szu-Hung, Chu, Li-Hsin, Huang, Yu-Hsuan, Kao, Wei-Te, Lei, Chieh-Han, Cheng, Chia-Yi, Lo, Chen-Kuan, Chen, Ling-Chun, Liu

Publikováno v: Asian Pacific journal of allergy and immunology. 29(3)

X-linked agammaglobulinemia (XLA, also called Bruton's disease) is is an X-linked recessive disorder characterized by recurrent bacterial infections, usually occurring in the first few years of life. Here, we report the results of a BTK gene mutation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cee03765a23f33deaa324545e5b40f2b
https://pubmed.ncbi.nlm.nih.gov/22053596

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Juvenile scleroderma: experience in one institution

Autor: Chia-Yi, Lo, Shyh-Dar, Shyur, Szu-Hung, Chu, Li-Hsin, Huang, Yu-Hsuan, Kao, Wei-Te, Lei, Chieh-Han, Cheng, Kuo-Hsi, Lee, Chen-Kuan, Chen, Ling-Chun, Liu

Publikováno v: Asian Pacific journal of allergy and immunology. 28(4)

Scleroderma is a chronic connective tissue disease characterized by hardened or scaly skin and widespread abnormalities of the viscera, which is rare in the pediatric age group.In this study, we retrospectively reviewed 23 pediatric patients sufferin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3debf371d4c2fa67e373e1e6dade0b02
https://pubmed.ncbi.nlm.nih.gov/21337913

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Dissertation/ Thesis

Research on the Rights of Liberty and Security of Person in ICCPR－Focusing on the implementation of the Domestic law in Japan.

Autor: Chia-Yi Lo, 羅佳怡

98
Regardless of past, present or future, Liberty of personal is one of human most important fundamental human rights.It is to be found with the Article 39, of the Magna Carta Libertatum: No free man shall be arrested, or imprisoned, or deprived

Externí odkaz: http://ndltd.ncl.edu.tw/handle/11824608502913863522