醫師介紹

Doctor Introduction

:::

醫師個人介紹

Syuan-Yu Hong
Syuan-Yu Hong

兒童神經科主治醫師

洪宣羽 Syuan-Yu Hong

兒童神經科主治醫師
宣羽醫師很喜歡和孩子相處,自醫學院畢業後即立志成為一名守護孩童健康的兒科醫師,平易近人且深入淺出的問診方式,準確找出問題的核心加以治療,對許多罕見的神經疾病有獨特見解。2013年取得兒科專科醫師資格後,便致力於兒童神經性疾病的研究,期許自己能為更多兒童的健康把關。
相關連結
學術論文

期刊論文

期刊論文/Journal Paper
(作者群,論文題目,期刊名稱,出版年月,卷號(期別):頁次起迄)
日期
1 傅如輝(Ru-Huei Fu)、吳柏彥(WU PO-YEN)、周宜卿(I-Ching Chou)、林建亨(Chien-Heng Lin)、洪宣羽(Syuan-Yu Hung)*,Demographic and Clinical Characteristics, Seizure Disorders, and Antiepileptic Drug Usage in Different Types of Corpus Callosum Disorders: A Comparative Study in Children,Italian Journal of Pediatrics,2024 Jan,50(20): 2024 . 01
2 傅如輝(Ru-Huei Fu)*、陳慧婕(Hui-Jye Chen)、洪宣羽(Syuan-Yu Hung),Glycine-Alanine Dipeptide Repeat Protein from C9-ALS Interacts with Sulfide Quinone Oxidoreductase (SQOR) to Induce the Activity of the NLRP3 Inflammasome in HMC3 Microglia: Irisflorentin Reverses This Interaction,Antioxidants,2023 Oct,12(10):1896 2023 . 10
3 傅如輝(Ru-Huei Fu)*、陳慧婕(Hui-Jye Chen)、洪宣羽(Syuan-Yu Hung),Interaction of the C9orf72-Amyotrophic Lateral Sclerosis-Related Proline–Arginine Dipeptide Repeat Protein with the RNA-Binding Protein NOVA1 Causes Decreased Expression of UNC13A Due to Enhanced Inclusion of Cryptic Exons, Which Is Reversed by Betulin Treatment,Cells,2023 Oct,12(20):2476 2023 . 10
4 傅如輝(Ru-Huei Fu)*、洪宣羽(Syuan-Yu Hung)、陳慧婕(Hui-Jye Chen)*,Syringin Improves 6-Hydroxydopamine Neurotoxicity and α-Synuclein Accumulation by Mediating MiR-34a/SIRT1/Beclin-1 Pathway and Activating Autophagy in SH-SY5Y Cells and Caenorhabditis elegans Model,Cells,2023 Sep,12(18):2310 2023 . 09
5 林建亨(Chien-Heng Lin)、(Tsai-Chun Hsiao)、陳傑賀(Chen, Chieh Ho)、陳佳雯(Jia-wen Chen)、莊子瑤(Tzu-Yao Chuang)、(Jeng-Shang Chang)、洪宣羽(Syuan-Yu Hung)*,A Single Center Observational Study of Spirometry Assessments in Children with Congenital Heart Disease after Surgery,Medicina-Lithuania,2023 Apr,59(4):764 2023 . 04
6 傅如輝(Ru-Huei Fu)*、洪宣羽(Syuan-Yu Hung)、(Chia-Wen Tsai)、劉詩平(Shih-Ping Liu)、邱紹智(Shao-Chih Chiu)、吳孟蓁(Wu, Meng-Zhen)、徐偉成(Woei-Cheang Shyu)、(Shinn-Zong Lin),Interaction of a Novel Alternatively Spliced Variant of HSD11B1L with Parkin Enhances the Carcinogenesis Potential of Glioblastoma: Peiminine Interferes with This Interaction,Cells,2023 Mar,12(6):894 2023 . 03
7 張鈺孜(Yu-Tzu Chang)、洪宣羽(Syuan-Yu Hung)、林瑋德(Wei-De Lin)、林建亨(Chien-Heng Lin)、林聖興(Sheng-Shing Lin)、蔡輔仁(Fuu-Jen Tsai)、周宜卿(I-Ching Chou)*,Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics,Children-Basel,2023 Mar,10(3):556 2023 . 03
8 林建亨(Chien-Heng Lin)、(Jung-Nien Lai)、(Inn-Chi Lee)、周宜卿(I-Ching Chou)、林瑋德(Wei-De Lin)、林美辰(Mei-Chen Lin)、洪宣羽(Syuan-Yu Hung)*,Kawasaki Disease May Increase the Risk of Subsequent Cerebrovascular Disease,STROKE,2022 Jan,53(): 2022 . 01
9 林建亨(Chien-Heng Lin)、林聖興(Sheng-Shing Lin)、洪宣羽(Syuan-Yu Hung)、陳傑賀(Chen, Chieh Ho)、周宜卿(I-Ching Chou)*,Lamotrigine Induced DRESS Syndrome in a Child: A Case Report and Literature Review,Children-Basel,2021 Nov,8(11):1063 2021 . 11
10 林建亨(Chien-Heng Lin)、陳傑賀(Chen, Chieh Ho)、洪宣羽(Syuan-Yu Hung)、周宜卿(I-Ching Chou)、梁信杰(Shinn-Jye Liang)、杭良文(Liang-Wen Hang)*,Polysomnography Is an Important Method for Diagnosing Pediatric Sleep Problems: Experience of One Children’s Hospital,Children-Basel,2021 Nov,(): 2021 . 11
11 林建亨(Chien-Heng Lin)、周宜卿(I-Ching Chou)、(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hung)*,Cytomegalovirus Infection in Infancy May Increase the Risk of Subsequent Epilepsy and Autism Spectrum Disorder in Childhood,Children-Basel,2021 Nov,8(1040): 2021 . 11
12 邱葳(CHIU, LI-WEI)、林聖興(Sheng-Shing Lin)、陳傑賀(Chen, Chieh Ho)、林建亨(Chien-Heng Lin)、李妮鍾(Lee, Ni-Chung)、洪宣羽(Syuan-Yu Hung)、周宜卿(I-Ching Chou)、林千琳(Chien-Lin Lin)、楊佩瑜(Pei-Yu Yang)*,NAXE gene mutation-related progressive encephalopathy: A case report and literature review,MEDICINE,2021 Oct,100(42):e27548 2021 . 10
13 林建亨(Chien-Heng Lin)、(Wei-De Lin)、(I-Ching Chou)、(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hung)*,Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?—A Retrospective Study,Life-Basel,2021 Aug,11(854): 2021 . 08
14 (Inn-Chi Lee)*、洪宣羽(Syuan-Yu Hung)、(Yi-Ho Weng)、(Yi-Ting Chen),Amplitude Integrated Electroencephalography and Continuous Electroencephalography Monitoring Is Crucial in High-Risk Infants and Their Findings Correlate With Neurodevelopmental Outcomes,Frontiers in Pediatrics,2021 Aug,3(9): 2021 . 08
15 林建亨(Chien-Heng Lin)、賴榮年(Jung-Nien Lai)、(Inn-Chi Lee)、周宜卿(I-Ching Chou)、林瑋德(Wei-De Lin)、林美辰(Mei-Chen Lin)、洪宣羽(Syuan-Yu Hung)*,Association Between Kawasaki Disease and Childhood Epilepsy: A Nationwide Cohort Study in Taiwan,Frontiers in Neurology,2021 Apr,(12): 2021 . 04
16 林建亨(Chien-Heng Lin)、陳傑賀(Chen, Chieh Ho)、洪宣羽(Syuan-Yu Hung)*、林聖興(Sheng-Shing Lin)、周宜卿(I-Ching Chou)、林曉娟(Hsiao-Chuan Lin)、張正成(Jeng-Sheng Chang),Comparison of severe pediatric complicated influenza patients with and without neurological involvement,MEDICINE,2021 Apr,100(17): 2021 . 04
17 林建亨(Chien-Heng Lin)、周宜卿(I-Ching Chou)、洪宣羽(Syuan-Yu Hung)*,Genetic factors and the risk of drug-resistant epilepsy in young children with epilepsy and neurodevelopment disability: A Prospective Study and Updated Meta-Analysis,MEDICINE,2021 Mar,100(12): 2021 . 03
18 洪宣羽(Syuan-Yu Hung)、(Jiann-Jou Yang)、(Shuan-Yow Li)、(Inn-Chi Lee)*,A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study,Journal of Personalized Medicine,2020 Dec,10(281): 2020 . 12
19 洪宣羽(Syuan-Yu Hung)、萬磊(Lei Wan)、林慧茹(Hui-Ju Lin)、林橙莉(Cheng-Li Lin)、魏長菁(Chang-Ching Wei)*,Long-Term Ambient Air Pollutant Exposure and Risk of Recurrent Headache in Children: A 12-Year Cohort Study,International Journal of Environmental Research and Public Health,2020 Dec,17(23):9140 2020 . 12
20 周宜卿(I-Ching Chou)、宋鴻樟(Fung-Chung J Sung)、洪宣羽(Syuan-Yu Hung)*,Incidence of epilepsy in children born prematurely and small for gestational age at term gestation: A population-based cohort study,JOURNAL OF PAEDIATRICS AND CHILD HEALTH,2020 Feb,56(2):324-329 2020 . 02
21 林建亨(Chien-Heng Lin)、林瑋德(Wei-De Lin)、周宜卿(I-Ching Chou)、李英齊(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hung)*,Infants of Mothers With Diabetes and Subsequent Attention Deficit Hyperactivity Disorder: A Retrospective Cohort Study,Frontiers in Pediatrics,2019 Nov,7(452): 2019 . 11
22 林建亨(Chien-Heng Lin)、林瑋德(Wei-De Lin)、周宜卿(I-Ching Chou)、李英齊(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hung)*,Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?,BMC Pediatrics,2019 Nov,19(406): 2019 . 11
23 林建亨(Chien-Heng Lin)、林瑋德(Wei-De Lin)、周宜卿(I-Ching Chou)、李英齊(Inn-Chi lee)、洪宣羽(Syuan-Yu Hung)*,Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study,Frontiers in Neurology,2019 May,10(528): 2019 . 05
24 林建亨(Chien-Heng Lin)、林瑋德(Wei-De Lin)、周宜卿(I-Ching Chou)、李英齊(Inn-Chi Lee)、范洪春(Hueng-Chuen Fan)、洪宣羽(Syuan-Yu Hung)*,Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications,BMC Neurology,2018 Sep,18(1):150 2018 . 09
25 林瑋德(Lin, Wei-De)、周宜卿(Chou, I-Ching)、蔡輔仁(Tsai, Fuu-Jen)、洪宣羽(Syuan-Yu Hong)*,A novel PIGA mutation in a Taiwanese family with early-onset epileptic encephalopathy,SEIZURE-EUROPEAN JOURNAL OF EPILEPSY,2018 Apr,58():52-54 2018 . 04
26 周宜卿(Chou, I-Ching)、李英齊(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hong)*,Basilar-type migraine: An overlooked cause of loss of consciousness in pediatric emergency rooms,Pediatrics and Neonatology,2017 Aug,(): 2017 . 08
27 李英齊(Inn-Chi Lee)、洪宣羽(Syuan-Yu Hong)*,Treatment of intractable seizure in Wolf-Hirschhorn syndrome with bromide,BRAIN & DEVELOPMENT,2017 Apr,(): 2017 . 04
28 洪宣羽(Syuan-Yu Hong)、辛裕隆(Yu-Long Xin)*、李英齊(Inn-Chi Lee)*,An Infant with Congenital Central Hypoventilation Syndrome: Transient Burst Suppression EEG,Pediatrics and Neonatology,2016 Aug,57(4):357-358 2016 . 08

研討會論文

研討會論文/Conference Papers
(發表主題或論文名稱,研討會名稱,演講地點,研討會期間,受邀演講題目)
日期
1 兒童族群不同類型胼胝體異常間的統計、表現、癲癇發作、及癲癇藥物使用比較,台灣兒科醫學會第256屆學術演講會,國立成功大學醫學院(成杏校區),2023.11.11~2023.11.12, 2023 . 11
2 台灣注意力不足過動症的全基因體關聯性研究,台灣兒科醫學會第256屆學術演講會,國立成功大學醫學院(成杏校區),2023.11.11~2023.11.12, 2023 . 11
3 用乾酪乳桿菌提取物誘導出川崎氏症小鼠模型並觀察其運動行為變化,台灣兒科醫學會第254藉學術演講會,台北國際會議中心,2023.04.22~2023.04.23, 2023 . 04
4 ,離子通道、構造、功能、與疾病通道蛋白病變”國際學術研討會,國立中興大學 生命醫學中心 1F大會議室,2022.11.5 ~2022.11.5 ,Genetic therapy in ion-channel disease 2022 . 11
5 ,International Symposium on “Ion channels: Structure, function, and disease-associated channelopathies,National Chung Hsing University, College of Life Science,2022.11.05~2022.11.06,Genetic therapy in ion channelopathies 2022 . 11
6 妥瑞症候群的全基因組關聯研究,台灣兒科醫學會第252屆學術演講會,台中榮民總醫院,2022.11.12~2022.11.13, 2022 . 11
7 ,AOCNA 2022 Virtual Symposium: Educational Program,Webex,2022.09.01~2022.09.02,Common neurological disorders at clinic 2022 . 09
8 ,Eisai Central Taiwan Childhood Epilepsy Forum,台中萬楓酒店,2022.08.20~2022.08.20,CLINICAL FEATURES of Temporal lobe epilepsy. 2022 . 08
9 胼胝體發育缺失患者的行為發展,臺灣兒科醫學會第250屆學術演講會,視訊會議,2022.04.16~2022.04.17, 2022 . 04
10 De novo Deletion Variants In The IRF2BPL Is Associated With Developmental Epileptic Encephalopathy,The 22nd Annual Meeting of the Infantile Seizure Society (ISS),Taipei International Convention Center (TICC), Taipei, Taiwan,2021.10.22~2021.10.24, 2021 . 10
11 Molecular Aspect of PRRT2 Gene Variation with Paroxysmal Kinesigenic Dyskinesia Patients in Central Taiwan,The 22nd Annual Meeting of the Infantile Seizure Society (ISS),Taipei International Convention Center (TICC), Taipei, Taiwan,2021.10.22~2021.10.24, 2021 . 10
12 Leigh syndrome presenting with nonconvulsive status epilepticus,The 22nd Annual Meeting of the Infantile Seizure Society (ISS),台北市,2021.10.22~2021.10.24, 2021 . 10
13 Sulfite oxidase deficiency and related disorders: Neuroimaging findings and genetic roles ,2021 International Symposium on Genetic Role of Neurometabolic Diseases with Infantile Epilepsy (ISGNIE) & The 22nd Annual Meeting of the Infantile Seizure Society (ISS),台灣 台北國際會議中心,2021.09.22~2021.10.24, 2021 . 09
14 Association Study of 212 Epileptic-related Genes Variation with Childhood Absence Epilepsy,台灣兒科醫學會第244屆學術演講會,台北榮民總醫院,2020.11.14~2020.11.15, 2020 . 11
15 Is preterm birth an aggravating factor for subsequent autism spectrum disorders and attention deficit hyperactivity disorder in children with febrile seizure?—A retrospective study,台灣兒科醫學會第240屆學術演講會,臺北國際會議中心,2019.11.09~2019.11.10, 2019 . 11
16 Association Study of 212 epileptic-related genes variation with Childhood Absence Epilepsy,2019 15th Asian and Oceanian Congress of Child Neurology,Shangri-La Hotel Kuala Lumpur, Malaysia.,2019.09.19~2019.09.22, 2019 . 09
17 Novel compound heterozygous mutation of the TBC1D24 gene in a Taiwanese infant with multifocal myoclonus and epilepsia partialis continua,The 20th Annual Meeting of Infantile Seizure Society,Nagoya Congress Center,2019.05.31~2019.06.01, 2019 . 05
18 ,台灣癲癇基因研究聯合小組會議,台中福華大飯店 5 樓 501 會議室,2019.02.23~2019.02.23,Novel compound heterozygous mutation of the TBC1D24 gene in a Taiwanese infant with multifocal myoclonus and epilepsia partialis continua 2019 . 02
19 Improving the Training Effect of Core Case Simulation Workshop in Pediatric Advanced Life Support Course with Standard Algorithms of 4 Critical Diseases,Critical Care Congress,San Diego Convention Center,2019.02.17~2019.02.20, 2019 . 02
20 Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications,16TH Asian Oceanian Congress of Neurology,COEX, Seoul, Korea from November 8-11, 2018.,2018.11.08~2018.11.11, 2018 . 11
21 Improving the Training Effect of Core Case Simulation Workshop in Pediatric Advanced Life Support Course with Standard Algorithms of 4 Critical Diseases,台灣兒科醫學會第二三六屆學術演講會,高雄醫學大學附設中和紀念醫院,2018.11.17~2018.11.18, 2018 . 11
22 Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications,台灣小兒神經醫學會第二十二次教育演講會,成大附設醫院 1 樓第三講堂,2018.11.04~2018.11.04, 2018 . 11
23 Childhood Stroke in One Children’s Hospital,台灣兒科醫學會第二三六屆學術演講會,國立成功大學成杏校區醫學院第三講堂,2018.11.17~2018.11.18, 2018 . 11
24 兒童期癲癇在早產兒以及低胎齡兒中的發生率:一個以族群為基礎的世代研究,臺灣兒科醫學會第二三四屆學術演講會,臺北國際會議中心,2018.04.21~2018.04.22, 2018 . 04
25 ,中區小兒癲癇研討會,Forchetta餐廳會議室,2017.11.11~2017.11.11,Case sharing: Epileptic encephalopathies in the era of genomic medicine 2017 . 11
26 Clinical and Genetic Studies in a Taiwanese Family with PIGA associated Epileptic Encephalopathy,臺灣兒科醫學會第232屆學術演講會,高雄醫學大學附設中和紀念醫院啟川大樓,2017.11.18~2017.11.19, 2017 . 11
27 Early-Onset Epileptic Encephalopathy Caused by Novel PIGA Mutation in a Taiwanese Family,台灣小兒神經醫學會第二十一次教育演講會,台北馬偕醫院15樓階梯講堂,2017.11.05~2017.11.05, 2017 . 11
28 Association Study of Ion Channel-related Genes Variation with childhood Absence Epilepsy,臺灣兒科醫學會第二三O屆學術演講會,臺北國際會議中心,2017.04.22~2017.04.23,Association Study of Ion Channel-related Genes Variation with childhood Absence Epilepsy 2017 . 04
29 自閉症與妥瑞症的風險相關性研究:以人口為基礎的世代研究The Risk Relevance of Autism Spectrum Disorders and Tourette Syndrome: A Population-Based Cohort Study,臺灣兒科醫學會第二二八屆學術演講會,台中榮民總醫院,2016.11.19~2016.11.20, 2016 . 11
30 Duchenne Muscular Dystrophy and Congenital Adrenal Insufficiency in two siblings,2016 15th Asian and Oceanian Myology Center Annual Scientific Meeting,National Chiao Tung University,2016.05.26~2016.05.29, 2016 . 05
31 Risk of Epilepsy in Type 1 Diabetes Mellitus: A Population-Based Cohort Study,台灣兒科醫學會第226屆學術演講會,台北國際會議中心,2016.04.23~2016.04.24, 2016 . 04
32 ,臺灣兒科醫學會第224屆學術演講會,台北國防醫學院,2015.11.14~2015.11.15, 2015 . 11

專書

暫無資料

研究計畫

研究計畫/Research Grant
(研究類型,研究計畫代號,主持人,補助或委託單位名稱,計畫名稱,計畫期間)
日期
1 個別型,C1111008-113,蔡輔仁(Fuu-Jen Tsai)、何道平、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、洪宣羽(Syuan Yu Hung)、鄧新棠、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu)、謝育芸、徐宜蓁,衛福部,112-114年罕見疾病特殊營養食品暨緊急需用藥物物流中心-113年後續擴充,2024.1.1~2024.12.31 2024 . 01
2 個別型,C1111009-113,蔡輔仁(Fuu-Jen Tsai)、楊美都(Mei-Due Yang)、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、藍先元(Hsien-Yuan Lane)、呂明桂(Ming-Kuei Lu)、林秀縵(LIN HSIU-MAN)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蘇旻昱(SU MIN-YU)、鄭雅靜(Ya-Chang,Cheng)、蔡教仁(Jiau-Ren Tsai)、林奕宇(LIN I-Yu)、呂孟純(Meng-Chun Lu)、童宜賢(Yi-Hsien Tung),衛福部,112年-114年罕見疾病照護服務計畫-113年後續擴充(分項2-北區),2024.1.1~2024.12.31 2024 . 01
3 個別型,C1111009-113,蔡輔仁(Fuu-Jen Tsai)、洪宣羽(Syuan Yu Hung)、楊美都(Mei-Due Yang)、林秀縵(LIN HSIU-MAN)、王仲興(Chung-Hsing Wang)、楊佩瑜(Pei-Yu Yang)、藍先元(Hsien-Yuan Lane)、林千琳(Chien-Lin Lin)、呂明桂(Ming-Kuei Lu)、蘇旻昱(SU MIN-YU)、蔡教仁(Jiau-Ren Tsai)、鄭雅靜(Ya-Chang,Cheng)、林奕宇(LIN I-Yu)、呂孟純(Meng-Chun Lu)、童宜賢(Yi-Hsien Tung),衛福部,112年-114年罕見疾病照護服務計畫-113年後續擴充(分項3-中區),2024.1.1~2024.12.31 2024 . 01
4 個別型,DMR-113-151,洪宣羽(Syuan-Yu Hung),附醫院內計畫,Pank2基因剔除小鼠的AAV9基因治療,2023.8.1~2024.7.31 2023 . 08
5 個別型,DMR-113-041,,附醫院內計畫,不同類型胼胝體疾病的人口統計學和臨床特徵、癲癇發作、抗癲癇藥物使用和功能磁共振成像結果:兒童研究比較,2023.8.1~2024.7.31 2023 . 08
6 個別型,C1111008,蔡輔仁(Fuu-Jen Tsai)、何道平、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、洪宣羽(Syuan Yu Hung)、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu),衛福部,112-114年罕見疾病特殊營養食品暨緊急需用藥物物流中心,2023.1.1~2023.12.31 2023 . 01
7 個別型,DMR-112-048,蔡輔仁(Fuu-Jen Tsai)、林瑋德(Wei-De Lin)、洪宣羽(Syuan-Yu Hung),附醫院內計畫,台灣妥瑞症候群的全基因組關聯研究,2022.8.1~2023.7.31 2022 . 08
8 個別型,C1080912-111,蔡輔仁(Fuu-Jen Tsai)、何道平、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、洪宣羽(Syuan-Yu Hung)、賴美月(Mei-Yueh Lai)、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu),衛福部,109年至111年罕見疾病特殊營養食品暨緊急需用藥物 物流中心-111年後續擴充,2022.1.1~2022.12.31 2022 . 01
9 個別型,C1081115-111,蔡輔仁(Fuu-Jen Tsai)、楊美都(Mei-Due Yang)、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、藍先元(Hsien-Yuan Lane)、呂明桂(Ming-Kuei Lu)、林秀縵(LIN HSIU-MAN)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蘇旻昱(SU MIN-YU)、鄭雅靜(Ya-Chang,Cheng)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,109-111年罕見疾病照護服務計畫-111年後續擴充(分項2-北區),2022.1.1~2022.12.31 2022 . 01
10 個別型,DMR-111-064,周宜卿(I-Ching Chou),附醫院內計畫,兒童和青年炎症性肌病異質性肌炎特異性抗體分析:從診斷到預後,2021.8.1~2022.7.31 2021 . 08
11 個別型,DMR-111-068,蔡輔仁(Fuu-Jen Tsai)、林瑋德(Wei-De Lin)、洪宣羽(Syuan-Yu Hung),附醫院內計畫,研究妥瑞症與強迫症之共同致病基因,2021.8.1~2022.7.31 2021 . 08
12 個別型,C1081115-110,蔡輔仁(Fuu-Jen Tsai)、楊美都(Mei-Due Yang)、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、藍先元(Hsien-Yuan Lane)、呂明桂(Ming-Kuei Lu)、林秀縵(LIN HSIU-MAN)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蘇旻昱(SU MIN-YU)、鄭雅靜(Ya-Chang,Cheng)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,109-111年罕見疾病照護服務計畫-110年後續擴充(分項2-北區),2021.1.1~2021.12.31 2021 . 01
13 個別型,C1081115-110,蔡輔仁(Fuu-Jen Tsai)、楊美都(Mei-Due Yang)、王仲興(Chung-Hsing Wang)、藍先元(Hsien-Yuan Lane)、呂明桂(Ming-Kuei Lu)、洪宣羽(Syuan-Yu Hung)、林秀縵(LIN HSIU-MAN)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蘇旻昱(SU MIN-YU)、蔡教仁(Jiau-Ren Tsai)、鄭雅靜(Ya-Chang,Cheng)、童宜賢(Yi-Hsien Tung),衛福部,109-111年罕見疾病照護服務計畫-110年後續擴充(分項3-中區),2021.1.1~2021.12.31 2021 . 01
14 個別型,C1080912-110,蔡輔仁(Fuu-Jen Tsai)、周宜卿(I-Ching Chou)、洪宣羽(Syuan-Yu Hung)、謝右文(Yow-Wen Hsieh)、何道平、賴美月(Mei-Yueh Lai)、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu),衛福部,109年至111年罕見疾病特殊營養食品暨緊急需用藥物物流中心-110年後續擴充,2021.1.1~2021.12.31 2021 . 01
15 個別型,DMR-110-061,蔡輔仁(Fuu-Jen Tsai)、林瑋德(Wei-De Lin)、洪宣羽(Syuan-Yu Hung),附醫院內計畫,基因性癲癎附加熱性痙攣症候羣之臨床光譜: 分析痙攣型態與藥物治療,2020.8.1~2021.7.31 2020 . 08
16 個別型,C1081115,蔡輔仁(Fuu-Jen Tsai)、彭慶添(Ching-Tien Peng)、傅雲慶(Fu, Yun-Ching)、楊美都(Mei-Due Yang)、王明鈺(Ming-Yu Wang)、王仲興(Chung-Hsing Wang)、洪宣羽(Syuan-Yu Hung)、鄭雅靜(Ya-Chang Cheng)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,109年-111年罕見疾病照護服務計畫(分項3:中區),2020.1.1~2022.12.31 2020 . 01
17 個別型,C1081115,蔡輔仁(Fuu-Jen Tsai)、彭慶添(Ching-Tien Peng)、傅雲慶(Fu, Yun-Ching)、楊美都(Mei-Due Yang)、王明鈺(Ming-Yu Wang)、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、鄭雅靜(Ya-Chang Cheng)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,109-111年罕見疾病照護服務計畫(分項2:北區),2020.1.1~2020.12.31 2020 . 01
18 個別型,C1080912,蔡輔仁(Fuu-Jen Tsai)、周宜卿(I-Ching Chou)、洪宣羽(Syuan-Yu Hung)、謝右文(Yow-Wen Hsieh)、何道平、賴美月(Mei-Yueh Lai)、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu),衛福部,109年至111年罕見疾病特殊營養食品暨緊急需用藥物物流中心,2020.1.1~2020.12.31 2020 . 01
19 個別型,DMR-109-042,周宜卿(I-Ching Chou),附醫院內計畫,透過Trio為基礎的全外顯子定序技術發現與神經退化性疾病相關的新候選基因,2019.8.1~2020.7.31 2019 . 08
20 個別型,C1060908-108,蔡輔仁(Fuu-Jen Tsai)、彭慶添(Ching-Tien Peng)、傅雲慶(Fu, Yun-Ching)、楊美都(Mei-Due Yang)、王明鈺(Ming-Yu Wang)、王仲興(Chung-Hsing Wang)、洪宣羽(Syuan-Yu Hung)、鄭雅靜(Ya-Chang Cheng)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,「罕見疾病照護服務計畫-108年後續擴充」(分項3:中區),2019.1.1~2019.12.31 2019 . 01
21 個別型,C1060908-108,蔡輔仁(Fuu-Jen Tsai)、彭慶添(Ching-Tien Peng)、傅雲慶(Fu, Yun-Ching)、楊美都(Mei-Due Yang)、王明鈺(Ming-Yu Wang)、王仲興(Chung-Hsing Wang)、周宜卿(I-Ching Chou)、鄭雅靜(Ya-Chang Cheng)、楊佩瑜(Pei-Yu Yang)、林千琳(Chien-Lin Lin)、蔡教仁(Jiau-Ren Tsai)、童宜賢(Yi-Hsien Tung),衛福部,「罕見疾病照護服務計畫-108年後續擴充」(分項2:北區),2019.1.1~2019.12.31 2019 . 01
22 個別型,C1051014-108,蔡輔仁(Fuu-Jen Tsai)、周宜卿(I-Ching Chou)、洪宣羽(Syuan-Yu Hung)、謝右文(Yow-Wen Hsieh)、何道平(He, Dao-Ping)、賴美月(Mei-Yueh Lai)、鄭啟在(Chi-Tsai Cheng)、呂孟純(Meng-Chun Lu),衛福部,106年至108年罕見疾病特殊營養食品暨緊急需用藥物物流中心-108年後續擴充,2019.1.1~2019.12.31 2019 . 01
23 個別型,MOST 107-2314-B-039-003,周宜卿(Chou, I-Ching)、李英齊,科技部,全基因外顯子定序在小兒神經基因性疾病中的應用,2018.4.1~2019.3.31 2018 . 04
24 個別型,DMR-107-052,周宜卿(I-Ching Chou),附醫院內計畫,性聯遺傳早期嬰兒型癲癇性腦病變: ㄧ群容易代代相傳的嚴重疾病,2017.8.1~2018.7.31 2017 . 08
25 個別型,DMR-106-168,李英齊(Inn-Chi Lee),附醫院內計畫,嬰幼兒癲癇性腦病變的原因分析,2016.8.1~2017.6.30 2016 . 08
26 個別型,DMR-105-121,蔡輔仁(Fuu-Jen Tsai)、王仲興(Chung-Hsing Wang)、林瑋德(Wei-De Lin)、張鈺孜(chang yu-tzu)、洪宣羽(Syuan-Yu Hong),附醫院內計畫,以次世代定序技術建立Dravet syndrome之基因診斷工具,2015.8.1~2016.7.31 2015 . 08

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(獲獎名稱,給獎單位,獲獎日期)
日期
1 年輕學者國際癲癇會議獎,台灣癲癇醫學會,2019.4.27 2019 . 04

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