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NBS.twNeonatal Screening Literature Database (NSdb).
http://www.nbs.tw/
Neonatal Screening Literature Database (NSdb).
http://www.nbs.tw/
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Neonatal Screening Literature Database (NSdb).
nbs.tw
Neonatal Screening Literature Database
http://www.nbs.tw/nsdb
Neonatal Screening Literature Database. Only by specified PMID(s). If the text area is kept empty, a browse with the following index/sub-topic constraints will be executed! Misspelled character (insertion, deletion, substitution) in the query. Limited to sub-topic about. Newborn screening project evaluation study. Congenital Adrenal Hyperplasia (CAH). Maple Syrup Urine Disease (MSUD). MediumChain Acyl-CoA Dehydrogenase Deficiency (MCAD). Glutaric Acidemia Type I (GA I). Citrullinemia type I (CIT).
新生兒先天性代謝異常疾病篩檢作業手冊
http://www.nbs.tw/assessment/nsmanual/index.htm
10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 16 Mar, 2012.
新生兒篩檢項目增減評估
http://www.nbs.tw/assessment
期間進行 國內新生兒先天異常疾病篩檢項目增減 可行性之探討 計畫編號 DOH92-HP-1210. 國內目前政策下常規的新生兒篩檢項目為 苯酮尿症 、 高胱 胺酸尿症. 半乳糖血症 、 先天性甲狀腺低能症 及 葡萄糖六 磷酸鹽去氫. 37238;缺乏症 ，近年來篩檢率已超過 99. 例如串聯質譜儀應用於新生兒先天性 胺基酸 和 有機酸 代謝異常疾病篩檢，為一省時省人力及增加篩檢項目的篩檢方法。 Updated: 2004.04.27). Updated: 2005.12.09). Updated: 2004.04.27). Updated: 2004.04.27). Updated: 2004.08.17). Updated: 2005.12.12). Updated: 2005.12.12). Updated: 2015.04.09). 10699 台北郵政 26-624 號信箱 電話 (02) 2703-6080 傳真 (02) 2703-6070. 09 Apr, 2015.
台灣地區新生兒篩檢之回顧與展望
http://www.nbs.tw/assessment/report_2005.htm
優生保健暨罕見疾病防治國際學術研討會 2005.12.10-11. Developments of Neonatal Screening in Taiwan. Department of Medical Research and Education, Taipei Veterans General Hospital,. Taipei, Taiwan 112. 篩檢項目為先天性甲狀腺低能症 (CHT)、苯酮尿症 (PKU)、楓漿尿病 (MSUD)、高胱胺酸尿症 (HCU)、半乳糖血症 (GAL) 等，篩檢作業系統中包括了檢體採集機構、新生兒篩檢中心、公共衛生護士追蹤網及負責確認診斷與治療的轉介醫院。 葡萄糖六磷酸鹽去氫 缺乏症 (G6PD) 的篩檢方法於1985年7月發展完成，併入執行中的全國新生兒篩檢作業進行先期篩檢，由兩年 (1985.7 1987.6) 的篩檢結果估算出台灣的G6PD缺乏症的發生率約為2% (男性3%，女性0.9%)。 台灣的新生兒篩檢率從最初的6.7% (1984年) ，1990年時達到80%，在1996年以後就已超過99%。 衛生署國民健康局於2003年委託評估探討 國內新生兒先...
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