Hiroyuki Hirose
Hiroyuki Hirose
[Recurrent posterior reversible encephalopathy due to vasospasm and cerebral hypoperfusionin in acute leukemia: a case report] [0.03%]
[急性白血病继发脑血管痉挛和脑低灌注所致复发性后可逆性脑病综合征1例]
Takuya Hiraide,Tomoko Matsubayashi,Hidetoshi Ishigaki et al.
Takuya Hiraide et al.
We report the case of a 4-year-old girl who presented with recurrent posterior reversible encephalopathy syndrome (PRES). She was diagnosed with B-precursor acute lymphocytic leukemia (ALL), and was administered remission-induction chemothe...
Case Reports
No to hattatsu = Brain and development. 2015 Nov;47(6):449-53. DOI: 2015
[A girl with dyslexia suspected to have Irlen syndrome, completely relieved by wearing tinted lenses] [0.03%]
[怀疑患有Irlen综合征的诵读困难女孩佩戴滤色镜后完全缓解]
Yusuke Kusano,Tomonari Awaya,Keiko Saito et al.
Yusuke Kusano et al.
Irlen syndrome is a proposed perceptual processing disorder characterized by visual distortions while reading. Patients with this syndrome may experience light sensitivity, visual stress, and other related problems such as dyslexia. Tinted ...
Case Reports
No to hattatsu = Brain and development. 2015 Nov;47(6):445-8. DOI: 2015
[Evaluation of surgical treatment for intractable aspiration in neurologically impaired patients: our experience with 20 patients] [0.03%]
神经系统障碍患者顽固性误吸的外科治疗效果评估(20例报告)
Mio Watanabe,Takashi Shiihara
Mio Watanabe
Objective: The present study aimed to evaluate the efficacy of surgical treatment for intractable aspiration in patients with severe motor and intellectual disabilities (SMID) and neuromuscular diseases (NMD). ...
Mieko Yoshioka
Mieko Yoshioka
Objective: The term benign congenital hypotonia is retrospective and refers to infants who are hypotonic at birth or shortly thereafter but later show a normal tone. It encompasses many different pathological processes th...
[Risk of seizure recurrence after a first unprovoked seizure in childhood] [0.03%]
[儿童首次发作无诱因癫痫后复发的风险]
Yuichi Takami,Eriko Satake,Hirofumi Ban
Yuichi Takami
Objective: To assess the risk of recurrence after a first unprovoked seizure in childhood. Methods: This was a prospective study of 250...
[Supplementation of L-carnitine to the severe motor and intellectual disabilities fed with enteral carnitine-deficient formulas for years] [0.03%]
长期服用全静脉或肠内营养 carnitine 缺乏配方的重度智体障碍患者补充左旋肉碱的安全性与有效性研究
Syuichi Tsuneishi,Kazuhiro Taguchi,Ryuzaburo Yagi
Syuichi Tsuneishi
Objective: We clarified the asymptomatic deficiency of serum free-carnitine in the severe motor and intellectual disabilities (SMIDs) fed with enteral carnitine-deficient formulas for years, and investigated the adequate ...
Clinical Trial
No to hattatsu = Brain and development. 2015 Nov;47(6):421-6. DOI: 2015
[Current situation and ethical-social issues of pediatric genetic testing] [0.03%]
[儿科遗传检测的现状与伦理-社会问题]
Toshiyuki Yamamoto
Toshiyuki Yamamoto
Many pediatric neurological disorders are caused by genetic factors. Therefore, genetic testing is often required for final diagnosis, prognosis prediction, and genetic counseling. Prior to performing genetic research, pediatric neurologist...
[A patient with multiple anomalies, growth deficiency, and developmental delay associated with a chromosomal balanced translocation] [0.03%]
[染色体平衡易位致多种异常、生长发育落后的患者一例]
Ayumi Matsumoto,Takanori Yamagata
Ayumi Matsumoto
Case Reports
No to hattatsu = Brain and development. 2015 Nov;47(6):413-4. DOI: 2015
Chitose Sugiura
Chitose Sugiura