Is hiragana decoding impaired in children with periventricular leukomalacia? [0.03%]
脑室周围白质软化患儿的hiragana解码障碍吗？
Naoko Kurahashi,Yukiko Futamura,Norie Nonobe et al.
Naoko Kurahashi et al.
Background: There are few studies on hiragana reading skill and phonological awareness in Japanese schoolchildren with periventricular leukomalacia (PVL). ...
Successful treatment of normokalemic periodic paralysis with hydrochlorothiazide [0.03%]
用氢氯噻嗪成功治疗正常血钾型周期性瘫痪患者
Yuichi Akaba,Satoru Takahashi,Yoshiaki Sasaki et al.
Yuichi Akaba et al.
Background: Periodic paralysis (PP) is an autosomal dominant muscle disorder characterized by periodic muscle weakness attacks associated with serum potassium level variations. It is classified into hypokalemic (hypoKPP),...
A case of tubulinopathy presenting with porencephaly caused by a novel missense mutation in the TUBA1A gene [0.03%]
TUBA1A基因错义新突变所致继发脑室周围白质软化症的管蛋白病1例
Tatsuharu Sato,Mitsuhiro Kato,Kaoru Moriyama et al.
Tatsuharu Sato et al.
Background: Tubulinopathies include a wide spectrum of disorders ranging from abnormal ocular movement to severe brain malformations, and typically present as diffuse agyria or perisylvian pachygyria with microcephaly, ag...
Radiotherapy for Langerhans cell histiocytosis with paraplegia: A rare oncologic emergency case report in infancy and literature review [0.03%]
朗格汉斯细胞组织细胞增生症并瘫痪的放射治疗一例及文献复习
Kentaro Nakashima,Yuhki Koga,Yasunari Sakai et al.
Kentaro Nakashima et al.
Background: Langerhans cell histiocytosis (LCH) is a clonal disease with focal or disseminated lesions that may compress the surrounding tissues, including the spinal cord. Because few reports have described the spinal sy...
ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease [0.03%]
ATP13A2的新突变引起一种少见的青少年型帕金森病
Jehan Suleiman,Nadia Hamwi,Ayman W El-Hattab
Jehan Suleiman
Parkinson disease is a common neurodegenerative disease that typically starts around the age of 60 years; however, juvenile-onset disease can occur rarely. Although Parkinson disease is typically sporadic; in rare occasions, it can be cause...
Extending the use of stiripentol to SLC13A5-related epileptic encephalopathy [0.03%]
司来磷酸钠在SLC13A5相关性癫痫性脑病中的应用扩展研究
Afnan Alhakeem,Faisal Alshibani,Brahim Tabarki
Afnan Alhakeem
Introduction: SLC13A5-related epileptic encephalopathy is a recently described autosomal recessive disorder that is characterized by infantile epilepsy and developmental delay. Seizures are markedly drug resistant and oft...
Long-term outcomes in motor and cognitive impairment with acute encephalopathy [0.03%]
急性脑病导致运动和认知障碍的长期预后
Yuri Matsubara,Hitoshi Osaka,Takanori Yamagata et al.
Yuri Matsubara et al.
Background: Acute encephalopathy causes various sequelae, including motor disabilities and intellectual delays. Previous studies reported that cognitive impairments can also occur after acute encephalitis. Although the in...
Influenza-associated neurological complications during 2014-2017 in Taiwan [0.03%]
台湾2014至2017年度流感相关神经并发症症状
Li-Wen Chen,Chao-Ku Teng,Yi-Shan Tsai et al.
Li-Wen Chen et al.
Introduction: Seasonal influenza-associated neurological complications had high mortality and morbidity rates in recent studies. We reported influenza-associated encephalitis/encephalopathy in children during 2014-2017 in...
Clinical characteristics of acute encephalopathy with acute brain swelling: A peculiar type of acute encephalopathy [0.03%]
急性脑肿胀性急性脑病的临床特征：一种特殊的急性脑病类型
Megumi Nukui,Hisashi Kawawaki,Takeshi Inoue et al.
Megumi Nukui et al.
Objectives: Acute encephalopathy has been observed with acute brain swelling (ABS) that is characterized by rapid progression to whole-brain swelling. The objective of this study was to describe the clinical characteristi...
Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG [0.03%]
两例以癫痫发作形式表现的儿童睡眠性瘫痪(附视频、脑电及肌电证据)
Tomoe Yanagishita,Susumu Ito,Yui Ohtani et al.
Tomoe Yanagishita et al.
Narcolepsy is characterized by excessive sleepiness, hypnagogic hallucinations, and sleep paralysis, and can occur with or without cataplexy. Here, we report two children with narcolepsy presenting with cataplexy mimicking epileptic seizure...