ホーム > 榎園 崇/ ENOKIZONO, Takashi
榎園 崇
ENOKIZONO, Takashi
小児科
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1.
A patient with peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and severe hypoganglionosis associated with a novel SOX10 mutation
Yuko Akutsu; Kentaro Shirai; Akira Takei; Yudai Goto (+9 著者) Ken Inoue
American Journal of Medical Genetics, Part A 176: 1195 (2018) Semantic Scholar
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2.
Preaxial polydactyly in an individual with Wiedemann-Steiner syndrome caused by a novel nonsense mutation in KMT2A
Takashi Enokizono; Tatsuyuki Ohto; Ryuta Tanaka; Mai Tanaka (+9 著者) Kenjiro Kosaki
AMERICAN JOURNAL OF MEDICAL GENETICS PART A 173: 2821 (2017) Semantic Scholar
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3.
Cyclic vomiting syndrome after acute autonomic and sensory neuropathy
Takashi Enokizono; Kiyotaka Nemoto; Junko Fujiwara; Ryuta TanakaTatsuyuki Ohto
PEDIATRICS INTERNATIONAL 59: 503 (2017) Semantic Scholar
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4.
A novel BBS10 mutation identified in a patient with Bardet-Biedl syndrome with a violent emotional outbreak.
Tatsuyuki Ohto; Takashi Enokizono; Ryuta Tanaka; Mai Tanaka (+8 著者) Kenjiro Kosaki
Human genome variation 4: 17033 (2017) Semantic Scholar
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5.
MLL2 and KDM6A Mutations in Patients With Kabuki Syndrome
Noriko Miyake; Eriko Koshimizu; Nobuhiko Okamoto; Seiji Mizuno (+38 著者) Norio Niikawa
AMERICAN JOURNAL OF MEDICAL GENETICS PART A 161: 2234 (2013) Semantic Scholar
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6.
Continuous regional arterial infusion effective for children with acute necrotizing pancreatitis even under neutropenia
Hiroko Fukushima; Takashi Fukushima; Ryoko Suzuki; Takashi Enokizono (+5 著者) Ryo Sumazaki
PEDIATRICS INTERNATIONAL 55: E11 (2013) Semantic Scholar
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7.
Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multi lobar Cortical Dysplasia-Three Case Reports-
Qin-Chuan Liang; Taisuke Otsuki; Akio Takahashi; Takashi Enokizono (+4 著者) Masayuki Sasaki
NEUROLOGIA MEDICO-CHIRURGICA 53: 47 (2013) Semantic Scholar
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