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Rare Disease Care Plan Information Session
110 years of education and training in rare disease care programs
Rare Disease Care Program Diversified Activities
Activities of Taiwan Multiple Sclerosis Association North District Patient Association
111-year supervision theme education training and case seminar
2022/08/02Education training and aromatherapy stress relief
Add Line for Rare Disease Care
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Rare Disease Care Handbook
Activities
2022
Niu Dau-Ming: Whole-gene sequencing can effectively prevent cancer and sudden death
Pompe disease treatment leads the world
Ministry of Health and Welfare Quarterly - Issue 33 2022.06
2021
"Fabry Disease Research and Treatment Center" won the SNQ Quality Mark Gold Award
Niu, Dau-Ming won the 31st Medical Dedication Award
Niu, Dau-Ming won the Medical Dedication Award, a clip of the press conference
Niu, Dau-Ming, winner of the Medical Service Award, clip of the award ceremony
The Hope of Rare Disease Patients
2020
2020 New Advances in Pediatric Medicine of the Chinese Medical Association
Good season Farm makes bamboo rice and pizza by itself
2019
108 year-end medical education and parent-child activities for patients
Williams Syndrome Association parent-child activities for patients
Director Niu Dau-Ming Fabry Disease domestic and foreign conferences
Hong Kong Pompe Disease Association visit
2018
Director Niu Dau-Ming Chinese Medical Association Fabry Disease domestic and foreign conferences
Director Dau-Ming Niu's 107 years of fruitful research results on Fabry Disease
Director Niu Dau-Ming's 2017 "Pompe Disease Medical Lecture"
Newborn’s blood looks like ‘strawberry milkshake’ Triglycerides rise to 20,000 and nearly fatal
2017
Director Dau-Ming Niu was invited to give lectures on Fabry disease in Japan
Director Niu, Dau-Ming participated in domestic and foreign medical conferences and shared records
(Reproduced from) TVBS report Niu, Dau-Ming director Fabry's disease - equipment donation ceremony
2016
Director Niu, Dau-Ming Fabry Disease Domestic and foreign conferences International exchanges
Reprinted from United Daily News - Niu, Dau-Ming, Newborn genetic testing actually saved this mother
2015
Director Dau-Ming Niu Fabry disease Symposium
Director Niu, Dau-Ming Taiwan-Japan Fabry disease Symposium
2014
Director Niu, Dau-Ming went to Fukuoka, Japan to share the Taiwan Fabry Disease experence
Niu, Dau-Ming attended International Conference on Fabry Disease
International Exchange Dr. Max J. Hilz from Germany visited and delivered a speech
2013
Director Dau-Ming Niu to International Conference on Fabry Syndrome in Spain
Director Dau-Ming Niu to Asia-Pacific Lysosome International Conference in Japan
Director Dau-Ming Niu gave a keynote speech at the Tokyo International Conference
Director Dau-Ming Niu Hosts International Symposium on Fabry Syndrome
Director Dau-Ming Niu Fabry's disease health education lecture
2012
Director Dau-Ming Niu Early detection of Fabry's disease blood test
Undertake the "Taiwan Fabry's Disease Clinical Trial Alliance" project
OPD consultation
Pompe disease consultation process
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Growth hormone stimulation test(Clonidine)
Horizontal gaze palsy with progressive scoliosis (HGPPS)
Sex hormone test and sex hormone medication hospitalization common questions and answers
Short-chain acyl-coenzyme A dehydrogenase deficiency; SCAD
Tyrosinemia type II
Glutaric acidemia type I fever and diarrhea emergency treatment
Citrullinemia type II
Hypothyroidism medication dose education sheet
Glycogen Storage Disease Type 1A
Precocious puberty health education sheet
Fabry Disease
Primary carnitine deficiency syndrome
Homocystinuria
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Kabuki Syndrome
Russell-Silver Syndrome
Pompe Disease
Overweight oral steroid suppression test outpatient common questions and answers
Logistics Center for Rare Disease Drugs and Food
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Calogen
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Phenyl Free 1
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2026-01-08
News
代謝及分子遺傳實驗室Sanger檢驗項目今2026/1/7(三)起全面恢復收件通知
2025-07-15
News
Notice of Temporary Suspension of Sanger Testing Services at the Metabolism and Molecular Genetics Laboratory-Starting, suspended from Tuesday July 15
2025-05-28
News
Assessment of bone age: This item is not currently covered by the National Health Insurance for children aged 7 years and above. The standard fee is NT$1,023.
2024-01-02
News
臺北榮民總醫院、道品股份有限公司、和鼎資産管理股份有限公司三方產學合作所開發的「精準醫療之基石-即時全基因分析系統」參加「財團法人生技醫療科技政策研究中心」所舉辦的第二十屆新創獎,榮獲「臨床新創獎」
2023-12-06
News
10秒完成大數據搜尋!臺北榮總打造全基因定序分析系統,還導入AI來預測用藥風險
2023-05-12
News
台北榮民總醫院 罕病照護計畫_《督導主題教育訓練暨分享會議》
2023-05-08
News
Pediatric nurse Li won the Nightingale Award for Outstanding Contribution Bronze Award
2023-01-30
News
Multiple Sclerosis North District Health Education Lecture 2023-02-11 (Sat) 1300-1700
2022-08-19
News
Establish your healthy and accurate genetic database in all aspects.
2022-06-23
News
Adjustment of the consultation time of the green channel of the special outpatient clinic
2022-06-20
News
20220711 Invite children and families to participate in family protection courses
2022-06-20
News
20220704 Let Love Illuminate the Rare - I Love Baby Garden Fair
2022-02-10
News
Niu, Dau-Ming: Whole-gene sequencing can effectively prevent cancer and sudden death
2022-01-18
News
Niu, Dau-Ming, director of Pediatric deeply involved in the research and treatment of rare diseases
2021-11-18
News
The hope of patients with rare diseases, medical field has dedicated 30 years without regret
2021-11-02
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照顧罕病兒不遺餘力 醫奉獎得主牛道明,頒獎典禮片段
2021-11-02
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北榮牛道明獲醫療奉獻獎殊榮,記者會片段
2021-10-29
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北榮牛道明 榮獲第31屆醫療奉獻獎
2021-10-27
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基因解碼與您的關係
2021-10-12
News
本院醫療團隊成功完成1歲3個月、9.8公斤幼兒器捐雙腎移植手術,幫助4歲李小妹妹(12公斤)及8歲許小妹妹(18公斤)脫離終生洗腎的痛苦,也創下國內最低體重的大愛器捐,並將兩顆腎臟分別植入的新紀錄!
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