榎園 崇(エノキゾノ タカシ)
- 所属
- 医学医療系
- 職名
- 講師
- URL
- 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
- A Case of Anorexia Nervosa with Focal Cortical Dysplasia
Nemoto Hiroki; Imagawa Kazuo; Enokizono Takashi; Masud...
Case reports in psychiatry/2024, 2024-04-01 - 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/194(7), 2024-02-26 - 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 - 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 - 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 - 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 - Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles
Okamoto Nobuhiko; Ohto Tatsuyuki; Enokizono Takashi; W...
CELLS/10(11), 2021-11 - 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 - 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 - 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 - Novel ARX mutation identified in infantile spasm syndrome patient
Takeshita Yohei; Ohto Tatsuyuki; Enokizono Takashi; Ta...
Human genome variation/7, 2020-03 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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
- A Case of Anorexia Nervosa with Focal Cortical Dysplasia
- 会議発表等
- 頭皮脳波では両側性異常が認められる頭頂葉てんかんに対する焦点診断と切除
田村剛一郎; 増田洋亮; 小野諒平; 榎園 崇; 西村光代; 石川栄一
第24回茨城小児神経内科外科懇話会/2023-12-16 - 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
- 頭皮脳波では両側性異常が認められる頭頂葉てんかんに対する焦点診断と切除
(最終更新日: 2024-09-09)