榎園 崇(エノキゾノ タカシ)

所属

医学医療系

職名

講師

URL

https://www.md.tsukuba.ac.jp/clinical-med/pediatrics/

研究分野

小児科学

研究キーワード

小児神経筋疾患
てんかん
神経発達症
微細神経学的徴候
認知機能

研究課題

てんかん患者のQOLの向上を目指して〜認知機能と微細神経学的徴候との関連〜	2023 -- 2025	榎園 崇	日本学術振興会/若手研究	3,510,000円
運動障害児童の書字障害に対する新規治療ストラテジーの構築	2021-04 -- 2023-03	大戸達之	/
小児の手指巧緻性機能障害に関する治療法の開発-磁気センサによる定量評価	2013-04 -- 2016-03	大戸達之	/

職歴

2023-07 -- (現在)	筑波大学医学医療系講師
2012-09 -- 2023-06	筑波大学附属病院病院講師
2012-04 -- 2012-08	筑波大学附属病院
2007-04 -- 2010-03	国立精神・神経医療研究センター病院
2003-05 -- 2010-03	筑波大学附属病院

学歴

1997-04 -- 2003-03	筑波大学医学専門学群

取得学位

2022-05	博士（医学）	筑波大学

免許資格等

2019-10	てんかん専門医
2015-11	小児神経専門医
2008-11	小児科専門医

所属学協会

-- (現在)	日本人類遺伝学会
-- (現在)	日本重症心身障害学会
-- (現在)	日本てんかん学会
-- (現在)	日本小児神経学会
-- (現在)	日本小児科学会

受賞

2019-09	AOCCN2019 Travel Award
2019-05	第61回日本小児神経学会学術集会　優秀口演賞
2011-05	第53回日本小児神経学会総会　若手優秀ポスター賞

論文

• Identification of a novel splice-site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy
  Nishino Megumi; Tanaka Mai; Imagawa Kazuo; Yaita Kats...
  American journal of medical genetics. Part A, 2024-02-26
  
  PubMed
• Posterior disconnection in early infancy to treat intractable epilepsy with multilobar cortical dysplasia: three case report
  Liang Qin-Chuan; Otsuki Taisuke; Takahashi Akio; Enoki...
  Neurologia medico-chirurgica/53(1)/pp.47-52, 2013-04-01
  
  PubMed
• Impact of COVID-19 pandemic on epilepsy care in Japan: A national-level multicenter retrospective cohort study
  Kuroda Naoto; Kubota Takafumi; Horinouchi Toru; Ikegay...
  Epilepsia open/7(3)/pp.431-441, 2022-05-28
  
  PubMed
• Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency
  Morita Atsushi; Enokizono Takashi; Ohto Tatsuyuki; Tan...
  Brain & development/43(3)/pp.475-481, 2021-03
  
  PubMed
• Boys with attention-deficit/hyperactivity disorder perform wider and fewer finger tapping than typically developing boys - Peer comparisons and the effects of methylphenidate from an exploratory perspective
  Enokizono Takashi; Ohto Tatsuyuki; Tanaka Mai; Maruo ...
  Brain and Development/44(3)/pp.189-195, 2021-11
  
  PubMed
• Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles
  Okamoto Nobuhiko; Ohto Tatsuyuki; Enokizono Takashi; W...
  CELLS/10(11), 2021-11
  
  PubMed
• Variants in KIF2A cause broad clinical presentation; the computational structural analysis of a novel variant in a patient with a cortical dysplasia, complex, with other brain malformations 3
  Hatano Maiko; Fukushima Hiroko; Ohto Tatsuyuki; Ueno ...
  American journal of medical genetics. Part A/185(4)/pp.1113-1119, 2021-01
  
  PubMed
• Association of Kabuki syndrome and tethered cord syndrome: a report of three cases and literature review
  Muroi Ai; Enokizono Takashi; Tsurubuchi Takao; Tsukada...
  Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery/37(4)/pp.1339-1343, 2020-07
  
  PubMed
• Quantitative assessment of fine motor skills in children using magnetic sensors
  Enokizono Takashi; Ohto Tatsuyuki; Tanaka Mai; Maruo ...
  Brain & development/42(6)/pp.421-430, 2020-03
  
  PubMed
• Novel ARX mutation identified in infantile spasm syndrome patient
  Takeshita Yohei; Ohto Tatsuyuki; Enokizono Takashi; Ta...
  Human genome variation/7, 2020-03
  
  PubMed
• A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2
  Saeki Saki; Enokizono Takashi; Imagawa Kazuo; Fukushim...
  CLINICAL CASE REPORTS/7(11)/pp.2059-2063, 2019-09
  
  PubMed
• A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay
  Ueno Yuichi; Enokizono Takashi; Fukushima Hiroko; Ohto...
  Human genome variation/6/p.25, 2019-05
  
  PubMed
• Schuurs-Hoeijmakers syndrome in two patients from Japan
  Hoshino Yusuke; Enokizono Takashi; Imagawa Kazuo; Tana...
  American journal of medical genetics. Part A/179(3)/pp.341-343, 2018-12
  
  PubMed
• Exonic deletions in are frequent in Japanese globoid-cell leukodystrophy patients
  Irahara-Miyana Kaori; Enokizono Takashi; Ozono Keiichi...
  Human genome variation/5/p.28, 2018-04
  
  PubMed
• A patient with peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and severe hypoganglionosis associated with a novel SOX10 mutation
  Akutsu Yuko; Shirai Kentaro; Takei Akira; Goto Yudai; ...
  American journal of medical genetics. Part A/176(5)/pp.1195-1199, 2018-05
  
  PubMed
• A novel BBS10 mutation identified in a patient with Bardet-Biedl syndrome with a violent emotional outbreak
  Ohto Tatsuyuki; Enokizono Takashi; Tanaka Ryuta; Tanak...
  Human genome variation/4, 2017-04
  
  PubMed
• Preaxial polydactyly in an individual with Wiedemann-Steiner syndrome caused by a novel nonsense mutation in KMT2A
  Enokizono Takashi; Ohto Tatsuyuki; Tanaka Ryuta; Tanak...
  American journal of medical genetics. Part A/173(10)/pp.2821-2825, 2017-08
  
  PubMed
• Cyclic vomiting syndrome after acute autonomic and sensory neuropathy
  Enokizono Takashi; Nemoto Kiyotaka; Fujiwara Junko; Ta...
  Pediatrics international : official journal of the Japan Pediatric Society/59(4)/pp.503-505, 2017-04
  
  PubMed
• MLL2 and KDM6A Mutations in Patients With Kabuki Syndrome
  Miyake Noriko; Koshimizu Eriko; Okamoto Nobuhiko; Mizu...
  AMERICAN JOURNAL OF MEDICAL GENETICS PART A/161(9)/pp.2234-2243, 2013-09
  
  PubMed
• Continuous regional arterial infusion effective for children with acute necrotizing pancreatitis even under neutropenia.
  Fukushima Hiroko; Fukushima Takashi; Suzuki Ryoko; Eno...
  Pediatrics International, 2013; 55:e11-3. doi: 10.1111/j.1442-200X.2012.03702.x./55(2)/pp.E11-E13, 2013-04
  
  PubMed

会議発表等

• 迷走神経刺激装置植え込み術後のImmediate responder
  荒木孝太; 増田洋亮; 西村光代; 榎園 崇
  日本脳神経外科学会第82回学術総会/2023-10-25--2023-10-27
• 迷走神経刺激装置植え込み術後のImmediate responder
  荒木孝太; 増田洋亮; 西村光代; 榎園 崇
  第55回日本てんかん学会学術集会/2023-10-19--2023-10-21

(最終更新日: 2024-02-11)