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Brain and Development
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2. Activation of leukocyte immunoglobulin-like receptor B2 signaling pathway in cortical lesions of pediatric patients with focal cortical dysplasia type IIb and tuberous sclerosis complex
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Tác giả
Jiong Yue, Chunqing Zhang, Xianjun Shi, Yujia Wei, ... Hui Yang.
Nội dung
Pages 829-838
2. Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment
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Tác giả
Sachiyo Fukushima, Ichiro Morioka, Shohei Ohyama, Kosuke Nishida, ... Hideto Yamada.
Nội dung
Pages 743-750
2. MicroRNA-31 regulating apoptosis by mediating the phosphatidylinositol-3 kinase/protein kinase B signaling pathway in treatment of spinal cord injury
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Tác giả
Yali Wang, Yitong Yuan, Yuantao Gao, Xiao Li, ... Chunfang Wang.
Nội dung
Pages 649-661
2. The developmental expression of metabotropic glutamate receptor 4 in prenatal human frontal lobe and neurogenesis regions
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Tác giả
Yan Xiang, Hua Han, Shengfeng Ji, Liang Wei, ... Junfeng Zhang.
Nội dung
Pages 567-576
2. Is the motor skills checklist appropriate for assessing children in Japan?
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Yosuke Kita, Fumiko Ashizawa, Masumi Inagaki.
Nội dung
Pages 483-489
2. Catch-up growth and behavioral development among preterm, small-for-gestational-age children: A nationwide Japanese population-based study
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Akihito Takeuchi, Takashi Yorifuji, Mariko Hattori, Kei Tamai, ... Hiroyuki Doi.
Nội dung
Pages 397-405
2. A longer body length and larger head circumference at term significantly influences a better subsequent psychomotor development in very-low-birth-weight infants
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Tomoko Egashira, Mizuko Hashimoto, Tada-aki Shiraishi, Akinori Shichijo, ... Toshimitsu Takayanagi.
Nội dung
Pages 313-319
2. Correlation between human nervous system development and acquisition of fetal skills: An overview
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Tác giả
Elisa Borsani, Anna Maria Della Vedova, Rita Rezzani, Luigi Fabrizio Rodella, Carlo Cristini.
Nội dung
Pages 225-233
2. Behavioral profiles in Rett syndrome: Data from the natural history study
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Tác giả
Caroline B. Buchanan, Jennifer L. Stallworth, Alexandra E. Scott, Daniel G. Glaze, ... Walter E. Kaufmann.
Nội dung
Pages 123-134
2. Everolimus for epilepsy and autism spectrum disorder in tuberous sclerosis complex: EXIST-3 substudy in Japan
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Tác giả
Masashi Mizuguchi, Hiroko Ikeda, Kuriko Kagitani-Shimono, Harumi Yoshinaga, ... Masaya Kubota.
Nội dung
Pages 1-10
3. Breastfeeding and risk of febrile seizures in infants: The Japan Environment and Children’s Study
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Tác giả
Naomi Mitsuda, Takatoshi Hosokawa, Masamitsu Eitoku, Mikiya Fujieda, ... Narufumi Suganuma.
Nội dung
Pages 839-847
3. Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder
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Tác giả
Yoshihiko Saito, Yoshimi Kaga, Eiji Nakagawa, Mariko Okubo, ... Masumi Inagaki.
Nội dung
Pages 751-759
3. Event-related potentials and behavior performance scores in children with sleep-disordered breathing
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Tác giả
Jiang Kaihua, Yi Yang, Zhao Fangqiao, Shen Huijuan, ... Dong Xuan.
Nội dung
Pages 662-670
3. Age-related differences in frontal lobe function in children with ADHD
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Tác giả
Akira Yasumura, Mikimasa Omori, Ayako Fukuda, Junichi Takahashi, ... Masumi Inagaki.
Nội dung
Pages 577-586
3. The association between brain morphological development and the quality of general movements
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Tomoki Maeda, Hajime Iwata, Kazuhito Sekiguchi, Mizuho Takahashi, Kenji Ihara.
Nội dung
Pages 490-500
3. Nutritional status among women whose pregnancy outcome was afflicted with neural tube defects in Tigray region of Ethiopia
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Tác giả
Abadi Leul Welderufael, Birhane Alem Berihu, Yibrah Berhe, Tony Magana, ... Afework Mulugeta.
Nội dung
Pages 406-412
3. Motor and cognitive development of children with Down syndrome: The effect of acquisition of walking skills on their cognitive and language abilities
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Tác giả
Yuko Yamauchi, Sayaka Aoki, Junko Koike, Naomi Hanzawa, Keiji Hashimoto.
Nội dung
Pages 320-326
3. Abnormal cortical activation during silent reading in adolescents with autism spectrum disorder
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Rei Ogawa, Kuriko Kagitani-Shimono, Junko Matsuzaki, Junpei Tanigawa, ... Masako Taniike.
Nội dung
Pages 234-244
3. Combining visual sensory functions and visuospatial orienting functions in children with visual pathology: A longitudinal study
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Tác giả
Marlou J.G. Kooiker, Hélène J.M. Verbunt, Johannes van der Steen, Johan J.M. Pel.
Nội dung
Pages 135-149
3. Maternal risk factors associated with neural tube defects in Tigray regional state of Ethiopia
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Tác giả
Birhane Alem Berihu, Abadi Leul Welderufael, Yibrah Berhe, Tony Magana, ... Kibrom Gebreselassie.
Nội dung
Pages 11-18
4. High incidence of status epilepticus and ongoing seizures on arrival to the hospital due to high prevalence of febrile seizures in Izumo, Japan: A questionnaire-based study
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Tác giả
Masahiko Kimura, Takeshi Taketani, Youichi Kurozawa.
Nội dung
Pages 848-853
4. Gender differences in occurrence of behavioral and emotional problems at the lower grades of elementary school: Association with developmental and behavioral characteristics at 5 years
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Yui Zen, Tomohiro Chiyonobu, Mariko Yuge, Isao Yokota, ... Hajime Hosoi.
Nội dung
Pages 760-768
4. Development and validation of a novel scoring system to predict severe intraventricular hemorrhage in very low birth weight infants
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Longkai He, Wei Zhou, Xiaopeng Zhao, Xiaoping Liu, ... Yanyan Song.
Nội dung
Pages 671-677
4. Clinical and neurodevelopmental features in children with cerebral palsy and probable congenital
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Zika Alessandra Carvalho, Carlos Brites, Ganeshwaran Mochida, Paloma Ventura, ... Rita Lucena.
Nội dung
Pages 587-594
4. Expert consensus on pharmacotherapy for tic disorders in Japan
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Yu Hamamoto, Miyuki Fujio, Maiko Nonaka, Natsumi Matsuda, ... Yukiko Kano.
Nội dung
Pages 501-506
4. Efficacy and safety of pyridoxal in West syndrome: A retrospective study
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Ryuki Matsuura, Shin-ichiro Hamano, Jun Kubota, Atsuro Daida, ... Reiko Koichihara.
Nội dung
Pages 413-419
4. Oxidant and antioxidant levels and DNA damage in tuberous sclerosis
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Mine Yuksel, Feyza Ustabas Kahraman, Sahbettin Selek, Omer Faruk Ozer, Akin Iscan.
Nội dung
Pages 245-249
4. Age related signal changes of the pituitary stalk on thin-slice magnetic resonance imaging in infants
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Takashi Okazaki, Tetsu Niwa, Keiji Suzuki, Shuhei Shibukawa, Yutaka Imai.
Nội dung
Pages 327-333
4. Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders
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Ayako Kashimada, Setsuko Hasegawa, Toshihiro Nomura, Hiroshi Shiraku, ... Masatoshi Takagi.
Nội dung
Pages 150-157
4. Neonatal seizures and white matter injury: Role of rotavirus infection and probiotics
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Jung Sook Yeom, Ji Sook Park, Young-Soo Kim, Rock Bum Kim, ... Chan-Hoo Park.
Nội dung
Pages 19-28
5. Developmental outcomes and prevalence of SLC2A1 variants in young infants with hypoglycorrhachia
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Wen-Hao Yu, Li-Wen Chen, Shan-Tair Wang, Yi-Fang Tu, Chao-Ching Huang.
Nội dung
Pages 854-861
5. Fetal growth restriction: From Polyvagal theory to developmental impairments?
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Vania Aldrete-Cortez, Adrián Poblano, Silvia A. Tafoya, Luz Angélica Ramírez-García, Cesar Casasola.
Nội dung
Pages 769-775
5. Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1
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Marie Glombova, Borivoj Petrak, Jiri Lisy, Josef Zamecnik, ... Petr Liby.
Nội dung
Pages 678-690
5. Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists
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Robertino Dilena, Paola De Liso, Matteo Di Capua, Dario Consonni, ... Dario Pruna.
Nội dung
Pages 595-599
5. Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly
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Mikako Enokizono, Noriko Sato, Miho Ota, Yoko Shigemoto, ... Hiroshi Matsuda.
Nội dung
Pages 507-515
5. The ketogenic diet for super-refractory status epilepticus patients in intensive care units
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Eu Gene Park, Jiwon Lee, Jeehun Lee.
Nội dung
Pages 420-427
5. Novel method using Hjorth mobility analysis for diagnosing attention-deficit hyperactivity disorder in girls
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Tác giả
Julie Chi Chow, Chen-Sen Ouyang, Ching-Tai Chiang, Rei-Cheng Yang, ... Lung-Chang Lin.
Nội dung
Pages 334-340
5. Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum
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A. Iodice, M. Carecchio, G. Zorzi, B. Garavaglia, ... C. Fusco.
Nội dung
Pages 250-256
5. Factors associated with electroencephalographic and clinical remission of benign childhood epilepsy with centrotemporal spikes
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Tác giả
Eun Hye Lee, Su-Jeong You.
Nội dung
Pages 158-162
5. Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification
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Tác giả
Chang-he Shi, Shuo Zhang, Zhi-hua Yang, Yu-tao Liu, ... Yu-ming Xu.
Nội dung
Pages 29-35
6. Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy
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Tác giả
Akiko Shibata, Mariko Kasai, Ai Hoshino, Taku Miyagawa, ... Masashi Mizuguchi.
Nội dung
Pages 862-869
6. Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
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Tác giả
Toshiyuki Yamamoto, Taichi Imaizumi, Keiko Yamamoto-Shimojima, Yongping Lu, ... Nobuhiko Okamoto.
Nội dung
Pages 776-782
6. Detailed clinical course of fatal acute encephalopathy in children
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Tác giả
Kazumi Tomioka, Masahiro Nishiyama, Hiroaki Nagase, Yusuke Ishida, ... Kazumoto Iijima.
Nội dung
Pages 691-698
6. Efficacy of phenobarbital for benign convulsions with mild gastroenteritis: A randomized, placebo-controlled trial
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Tác giả
Yuichi Takami, Taku Nakagawa.
Nội dung
Pages 600-603
6. Serum carnitine levels of children with epilepsy: Related factors including valproate
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Akihisa Okumura, Hirokazu Kurahashi, Hideyuki Iwayama, Shingo Numoto.
Nội dung
Pages 516-521
6. Recreational nitrous oxide abuse related subacute combined degeneration of the spinal cord in adolescents – A case series and literature review
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Tác giả
Shih-Yun Lan, Cheng-Yen Kuo, Cheng-Che Chou, Shu-Sing Kong, ... Kuang-Lin Lin.
Nội dung
Pages 428-435
6. Sensory processing in children with autism spectrum disorder and the mental health of primary caregivers
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Kanae Suzuki, Shu Takagai, Masatsugu Tsujii, Hiroyuki Ito, ... Kenji J. Tsuchiya.
Nội dung
Pages 341-351
6. Three Japanese patients with 3p13 microdeletions involving FOXP1
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Tác giả
Keiko Yamamoto-Shimojima, Nobuhiko Okamoto, Wataru Matsumura, Tetsuya Okazaki, Toshiyuki Yamamoto.
Nội dung
Pages 257-262
6. The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children
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Tác giả
Shinichi Magara, Takao Komatsubara, Moemi Hojo, Yu Kobayashi, ... Jun Tohyama.
Nội dung
Pages 163-172
6. Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan
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Kentaro Okamoto, Mitsumasa Fukuda, Isao Saito, Risako Urate, ... Hisahide Nishio.
Nội dung
Pages 36-42
7. A severe case of Menkes disease with repeated bone fracture during the neonatal period, followed by multiple arterial occlusion
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Tác giả
Satoru Kobayashi, Kyoko Yokoi, Naomi Kamioka, Naoki Hamajima, ... Satoshi Suzuki.
Nội dung
Pages 878-882
7. Phenotypic manifestations between male and female children with CDKL5 mutations
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Tác giả
Jao-Shwann Liang, Hsin Huang, Jinn-Shyan Wang, Jyh-Feng Lu.
Nội dung
Pages 783-789
7. Epileptic spasm and other forms of epilepsy in presumed perinatal arterial ischemic stroke in Turkey after more than 10 years follow-up: A single centre study
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Tác giả
Gonca Bektaş, Osman Kipoğlu, Edibe Pembegül Yıldız, Nur Aydınlı, ... Serra Sencer.
Nội dung
Pages 699-705
7. Predicting the outcomes of targeted temperature management for children with seizures and/or impaired consciousness accompanied by fever without known etiology
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Tác giả
Tsukasa Tanaka, Hiroaki Nagase, Hiroshi Yamaguchi, Yusuke Ishida, ... Kazumoto Iijima.
Nội dung
Pages 604-613
7. Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome
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Tác giả
Giovanna Lenci, Maria Grazia Calevo, Roberto Gaggero, Giulia Prato, ... Edvige Veneselli.
Nội dung
Pages 522-530
7. Clinical manifestations, treatment outcomes, and prognostic factors of pediatric anti-NMDAR encephalitis in tertiary care hospitals: A multicenter retrospective/prospective cohort study
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Tác giả
Napa Pruetarat, Wiracha Netbaramee, Siriporn Pattharathitikul, Montida Veeravigrom.
Nội dung
Pages 436-442
7. Resting energy expenditure prediction using bioelectrical impedance analysis in patients with severe motor and intellectual disabilities
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Tác giả
Naoki Hashizume, Yoshiaki Tanaka, Motomu Yoshida, Suguru Fukahori, ... Yushiro Yamashita.
Nội dung
Pages 352-358
7. A nationwide survey of norovirus-associated encephalitis/encephalopathy in Japan
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Tác giả
Taiki Shima, Akihisa Okumura, Hirokazu Kurahashi, Shingo Numoto, ... Toshiaki Shimizu.
Nội dung
Pages 263-270
7. Effects of human umbilical cord blood CD34+ cell transplantation in neonatal hypoxic-ischemia rat model
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Tác giả
Yan Yu, YiZhong Yan, Zhen Luo, Pan Luo, ... LaMei Cheng.
Nội dung
Pages 173-181
7. Renal dysfunction is rare in Fukuyama congenital muscular dystrophy
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Tác giả
Keiko Ishigaki, Ikuko Kato, Terumi Murakami, Takatoshi Sato, ... Satoru Nagata.
Nội dung
Pages 43-49
8. ARX-associated infantile epileptic-dyskinetic encephalopathy with responsiveness to valproate for controlling seizures and reduced activity of muscle mitochondrial complex IV
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Tác giả
Anna Ka-Yee Kwong, Vanessa Loi-Yan Chu, Richard J.T. Rodenburg, Jan Smeitink, Cheuk-Wing Fung.
Nội dung
Pages 883-887
8. Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy
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Tác giả
Naomi Hino-Fukuyo, Kazuhiro Haginoya, Toshiyuki Takahashi, Ichiro Nakashima, ... Shigeo Kure.
Nội dung
Pages 790-795
8. Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10
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Tác giả
Ali Mir, Mohammed Chaudhary, Hani Alkhaldi, Rami Alhazmi, ... Yousef Housawi.
Nội dung
Pages 706-715
8. Clinical analysis of psychiatric symptoms of Japanese encephalitis during the convalescent Period: A single center study in Chongqing, China
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Tác giả
Maoling Yang, Nong Xiao, Shuang Chen, Wei Jiang.
Nội dung
Pages 614-617
8. Clinical time course of pediatric acute disseminated encephalomyelitis
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Tác giả
Masahiro Nishiyama, Hiroaki Nagase, Kazumi Tomioka, Tsukasa Tanaka, ... Kazumoto Iijima.
Nội dung
Pages 531-537
8. Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan
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Tác giả
Akihisa Okumura, Harushi Mori, Pin Fee Chong, Ryutaro Kira, ... Keiko Tanaka-Taya.
Nội dung
Pages 443-451
8. Treatment options in pediatric super-refractory status epilepticus
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Tác giả
Palita Arayakarnkul, Krisnachai Chomtho.
Nội dung
Pages 359-366
8. Reversible splenial lesion syndrome in children with benign convulsions associated with mild gastroenteritis: A retrospective study of five cases
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Tác giả
Lihua Jiang, Shanshan Mao, Jialu Xu, Feng Gao.
Nội dung
Pages 271-275
8. Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation
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Tác giả
Mona Entezam, Masoumeh Razipour, Saeed Talebi, Mehran Beiraghi Toosi, Mohammad Keramatipour.
Nội dung
Pages 182-186
8. Characteristics of Japanese patients with X-linked adrenoleukodystrophy and concerns of their families from the 1st registry system
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Tác giả
Ken Sakurai, Toya Ohashi, Nobuyuki Shimozawa, Seo Joo-Hyun, ... Hiroyuki Ida.
Nội dung
Pages 50-56
9. A 16q22.2-q23.1 deletion identified in a male infant with West syndrome
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Tác giả
Tatsuo Mori, Aya Goji, Yoshihiro Toda, Hiromichi Ito, ... Shoji Kagami.
Nội dung
Pages 888-893
9. Cumulative jerk as an outcome measure in nonambulatory Duchenne muscular dystrophy
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Tác giả
Tatsuya Fujii, Eri Takeshita, Yasuyuki Iwata, Hiroyuki Yajima, ... Tomohiro Kumada.
Nội dung
Pages 796-802
9. Corrigendum to “Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10” [Brain Dev 2019]
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Tác giả
Ali Mir, Mohammed Chaudhary, Hani Alkhaldi, Rami Alhazmi, ... Yousef Housawi.
Nội dung
Page 716
9. Early administration of vitamins B1 and B6 and l-carnitine prevents a second attack of acute encephalopathy with biphasic seizures and late reduced diffusion: A case control study
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Tác giả
Kana Okazaki Fukui, Masaya Kubota, Hiroshi Terashima, Akira Ishiguro, Hirofumi Kashii.
Nội dung
Pages 618-624
9. Two unrelated girls with intellectual disability associated with a truncating mutation in the PPM1D penultimate exon
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Tác giả
Yukiko Kuroda, Hiroaki Murakami, Takayuki Yokoi, Tatsuro Kumaki, ... Kenji Kurosawa.
Nội dung
Pages 538-541
9. Phenotypic features of 1q41q42 microdeletion including WDR26 and FBXO28 are clinically recognizable: The first case from Japan
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Tác giả
Tomoe Yanagishita, Keiko Yamamoto-Shimojima, Sayaka Nakano, Testuya Sasaki, ... Toshiyuki Yamamoto.
Nội dung
Pages 452-455
9. MRI findings in pediatric neuromyelitis optica spectrum disorder with MOG antibody: Four cases and review of the literature
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Tác giả
Azusa Ikeda, Yoshihiro Watanabe, Hikari Kaba, Kimihiko Kaneko, ... Saoko Takeshita.
Nội dung
Pages 367-372
9. A novel mutation in the GATAD2B gene associated with severe intellectual disability
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Tác giả
Kimiko Ueda, Kumiko Yanagi, Tadashi Kaname, Nobuhiko Okamoto.
Nội dung
Pages 276-279
9. Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia
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Tác giả
Tsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, Kenichiro Hata.
Nội dung
Pages 187-190
9. Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survival
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Tác giả
Nuha Al Zaabi, Anoud Kendi, Fatma Al-Jasmi, Shigeo Takashima, ... Osama Y. Al-Dirbashi.
Nội dung
Pages 57-65
10. Neuropsychological outcomes of childhood acute necrotizing encephalopathy
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Tác giả
Tracey A. Williams, Ruth K. Brunsdon, Karen L.O. Burton, Suzi Drevensek, ... Shekeeb S. Mohammad.
Nội dung
Pages 894-900
10. Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C
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Tác giả
Atsuko Kori, Ikumi Hori, Tatsushi Tanaka, Kohei Aoyama, ... Shinji Saitoh.
Nội dung
Pages 803-807
10. A case of early myoclonic encephalopathy with intractable seizures successfully treated with high-dose phenobarbital
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Tác giả
Takuya Kosaka, Genrei Ohta, Hiroshi Kometani, Masao Kawatani, Yusei Ohshima.
Nội dung
Pages 717-720
10. Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome
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Tác giả
Aya Hashimoto, Ichiro Kuki, Masataka Fukuoka, Kiyohiro Kim, ... Shinji Saitoh.
Nội dung
Pages 625-629
10. Neuronal ceroid lipofuscinosis type-11 in an adolescent
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Tác giả
Mahesh Kamate, Mayank Detroja, Virupaxi Hattiholi.
Nội dung
Pages 542-545
10. Electroencephalographic and epilepsy findings in mecp2 duplication syndrome. A family study
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Tác giả
Federica Lotti, Ursula Geronzi, Salvatore Grosso.
Nội dung
Pages 456-459
10. Fulminant acute disseminated encephalomyelitis in children
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Tác giả
Yukako Yae, Go Kawano, Takaoki Yokochi, Toru Imagi, ... Toyojiro Matsuishi.
Nội dung
Pages 373-377
10. A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis
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Tác giả
Hiroki Tsuchiya, Tomoyuki Akiyama, Tomiko Kuhara, Yoko Nakajima, ... Katsuhiro Kobayashi.
Nội dung
Pages 280-284
10. Severe neurologic and hepatic toxicity in a newborn prenatally exposed to methamphetamine. A case report
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Tác giả
Eugenia Maranella, Arianna Mareri, Valentina Nardi, Cecilia Di Natale, ... Sandra Di Fabio.
Nội dung
Pages 191-194
10. Cyclic alternating pattern in infants with congenital hypothyroidism
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Tác giả
Rafael Santana-Miranda, Chiharu Murata, Oliveiro Bruni, Agostinho Rosa, ... Javier Velazquez-Moctezuma.
Nội dung
Pages 66-71
11. Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease
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Tác giả
Marc Nikolaus, Anna Tietze, Leonille Schweizer, Angela M. Kaindl, ... Ellen Knierim.
Nội dung
Pages 901-904
11. Usefulness of diagnostic tools in a GLUT1 deficiency syndrome patient with 2 inherited mutations
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Tác giả
Blandine Dozières-Puyravel, Sasha Zaman, Steven Petrou, Laurent François, ... Stéphane Auvin.
Nội dung
Pages 808-811
11. Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy
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Tác giả
Tomonori Ishiguro, Yuichiro Sugiyama, Kazuto Ueda, Yukako Muramatsu, ... Masahiro Hayakawa.
Nội dung
Pages 721-725
11. Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report
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Tác giả
Tomoko Mizuno, Ayako Kashimada, Toshihiro Nomura, Kengo Moriyama, ... Shuki Mizutani.
Nội dung
Pages 630-633
11. Early enzyme replacement therapy enables a successful hematopoietic stem cell transplantation in mucopolysaccharidosis type IH: Divergent clinical outcomes in two Japanese siblings
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Narutoshi Yamazaki, Motomichi Kosuga, Kazuhiro Kida, Go Takei, ... Torayuki Okuyama.
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Pages 546-550
11. A case of Niemann-Pick disease type C with neonatal liver failure initially diagnosed as neonatal hemochromatosis
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Tadayuki Kumagai, Hiroshi Terashima, Hajime Uchida, Akinari Fukuda, ... Masaya Kubota.
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Pages 460-464
11. An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome
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Sayaka Okuzono, Ryoko Fukai, Marie Noda, Noriko Miyake, ... Shouichi Ohga.
Nội dung
Pages 378-381
11. A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant
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Naoko Ishihara, Hidehito Inagaki, Misa Miyake, Yoshiki Kawamura, ... Hiroki Kurahashi.
Nội dung
Pages 285-291
11. Aggregate formation analysis of GFAPR416W found in one case of Alexander disease
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Janyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, Hiroko Shimbo, ... Hitoshi Osaka.
Nội dung
Pages 195-200
11. The effects of antihistamines on the semiology of febrile seizures
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Michihiko Takasu, Tetsuo Kubota, Takeshi Tsuji, Hirokazu Kurahashi, ... Akihisa Okumura.
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Pages 72-76
12. Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing
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Ayaka Hirasawa-Inoue, Akihiko Ishiyama, Eri Takeshita, Yuko Shimizu-Motohashi, ... Masayuki Sasaki.
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Pages 905-909
12. Novel RASA1 mutations in Japanese pedigrees with capillary malformation-arteriovenous malformation
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Yosuke Moteki, Hiroyuki Akagawa, Yasunari Niimi, Yoshikazu Okada, Takakazu Kawamata.
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Pages 812-816
12. Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutation
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Ayumi Matsumoto, Masako Nagashima, Kazuhiro Iwama, Takeshi Mizuguchi, ... Hitoshi Osaka.
Nội dung
Pages 726-730
12. Hyperammonemia in a case of herpes simplex and anti-N-methyl-d-aspartate receptor encephalitis
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Jung Min Ko, Woo Joong Kim, Soo Yeon Kim, Jun Hwa Lee, ... Byung Chan Lim.
Nội dung
Pages 634-637
12. Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis
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Kyoko Hazama, Takashi Shiihara, Hiroyuki Tsukagoshi, Takeshi Matsushige, ... Mio Watanabe.
Nội dung
Pages 551-554
12. MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene
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Mari Kuwajima, Masahide Goto, Koyuru Kurane, Hiroko Shimbo, ... Hitoshi Osaka.
Nội dung
Pages 465-469
12. Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract
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Jun Kido, Takaaki Sawada, Ken Momosaki, Yosuke Suzuki, ... Shirou Matsumoto.
Nội dung
Pages 382-388
12. Concentrations of various forms of vitamin B6 in ginkgo seed poisoning
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Tomomitsu Sado, Setsuko Nakata, Takahisa Tsuno, Masanori Sato, ... Keiji Wada.
Nội dung
Pages 292-295
12. X-linked Charcot–Marie–Tooth disease type 5 with recurrent weakness after febrile illness
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Noriko Nishikura, Takanori Yamagata, Takao Morimune, Jun Matsui, ... Yoshihiro Maruo.
Nội dung
Pages 201-204
12. Risk factors of cognitive impairment in pediatric epilepsy patients with focal cortical dysplasia
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Nobusuke Kimura, Yukitoshi Takahashi, Hideo Shigematsu, Katsumi Imai, ... Yushi Inoue.
Nội dung
Pages 77-84
13. Announcements and Reports
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Nội dung
Pages I-II
13. Perampanel attenuates myoclonus in a patient with neuronal ceroid lipofuscinoses type 2 disease
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Lee Chin Wong, Chia-Jui Hsu, Wang-Tso Lee.
Nội dung
Pages 817-819
13. Longitudinal magnetic resonance imaging changes in Japanese encephalitis
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Yukie Arahata, Katsunori Fujii, Tatsuya Nishimura, Tomoko Uchida, ... Akihito Honda.
Nội dung
Pages 731-734
13. Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report
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Kenji Yamada, Michinori Ito, Hironori Kobayashi, Yuki Hasegawa, ... Takeshi Taketani.
Nội dung
Pages 638-642
13. Brain stem infarction in a 6-year-old boy with Down syndrome
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Toru Imagi, Tomonaga Matsushita, Miyuki Matsushita, Yukako Yae, ... Toyojiro Matsuishi.
Nội dung
Pages 555-558
13. Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutation
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Chihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, Yukari Endo, ... Yuji Takahashi.
Nội dung
Pages 470-473
13. Ketogenic diet as a successful early treatment modality for SCN2A mutation
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Dilsad Turkdogan, Gulten Thomas, Birsen Demirel.
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Pages 389-391
13. Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome
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Sotaro Kanai, Tohru Okanishi, Ayataka Fujimoto, Shinji Itamura, ... Hideo Enoki.
Nội dung
Pages 296-300
13. Clasmatodendrosis is associated with dendritic spines and does not represent autophagic astrocyte death in influenza-associated encephalopathy
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Masaya Tachibana, Ikuko Mohri, Ikuko Hirata, Ayano Kuwada, ... Masako Taniike.
Nội dung
Pages 85-95
13. A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiency
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Lifang Dai, Changhong Ding, Fang Fang.
Nội dung
Pages 205-209
14. Cover
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Nội dung
Page IBC
14. Central nervous system vasculitis from Epstein-Barr virus-associated T/natural killer-cell lymphoproliferative disorder in children: A case report
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Mi Seon Lee, Su-Kyeung Hwang, Yeong Eun Kim, Jin Kyung Suh, ... Yun Jeong Lee.
Nội dung
Pages 820-825
14. Anterior cingulate cortex involvement in non-paraneoplastic limbic encephalitis
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Kyosuke Ibi, Katsunori Fujii, Hironobu Kobayashi, Masayoshi Senda, ... Akihito Honda.
Nội dung
Pages 735-739
14. Corrigendum to “Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum” [Brain Dev. 41 (2019) 250–256]
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A. Iodice, M. Carecchio, G. Zorzi, B. Garavaglia, ... C. Fusco.
Nội dung
Page 643
14. A case of confusional migraine with transient increased cerebral blood flow
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Emiko Momoki, Tatsuo Fuchigami, Yuki Kasuga, Kaori Kimura, ... Ichiro Morioka.
Nội dung
Pages 559-562
14. Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases
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Takuya Hiraide, Tsutomu Ogata, Seiji Watanabe, Mitsuko Nakashima, ... Hirotomo Saitsu.
Nội dung
Pages 474-479
14. Spontaneous spinal epidural hematoma mimicking Guillain-Barre Syndrome
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Aya Kondo, Hiroshi Yamaguchi, Yusuke Ishida, Daisaku Toyoshima, ... Azusa Maruyama.
Nội dung
Pages 392-395
14. Severe anti-GAD antibody-associated encephalitis after stem cell transplantation
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Koki Nagai, Takanobu Maekawa, Hiroshi Terashima, Masaya Kubota, Akira Ishiguro.
Nội dung
Pages 301-304
14. Transient extreme spindles in a young child with anti-NMDAR encephalitis: A case report
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Sachi Tokunaga, Minako Ide, Takehiro Ishihara, Takako Matsumoto, ... Takeo Kato.
Nội dung
Pages 210-213
14. Risk factors and motor outcome of paediatric stroke patients
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Zeynep Selen Karalok, Hulya Maras Genc, Birce Dilge Taskin, Nesrin Ceylan, ... Nese Yarali.
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Pages 96-100
15. Contents
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Nội dung
Page OBC
15. Letter to the editor
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Natan Gadoth.
Nội dung
Page 826
15. The risk of hypoglycemia and the ketogenic diet for super-refractory status epilepticus patients
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Klára Brožová, Jan Brož.
Nội dung
Page 740
15. Methotrexate myelopathy
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Priyanka Madaan, Lokesh Saini.
Nội dung
Pages 644-645
15. General movements: Longitudinal assessment better than cross-sectional
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Lokesh Saini, Priyanka Madaan, M.R. Rudresh Naik.
Nội dung
Pages 563-564
15. Poor clinico-radiological correlation: A hallmark of acute flaccid myelitis
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Priyanka Madaan, Shivan Keshavan, Lokesh Saini.
Nội dung
Pages 480-481
15. Announcements and reports
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Nội dung
Page I
15. Acute encephalopathy with biphasic seizures and late reduced diffusion accompanied by Takotsubo cardiomyopathy
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Hiroshi Yamaguchi, Hiroaki Nagase, Shinobu Yoshida, Shoichi Tokumoto, ... Kazumoto Iijima.
Nội dung
Pages 305-309
15. Transient posterior cerebral arteriopathy: An unusual case enterovirus-related
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Benedetta Piccolo, Marina Barsacchi, Francesca Greco, Davide Cerasti, ... Francesco Pisani.
Nội dung
Pages 214-216
15. A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images – A first case of CLCN2-related leukoencephalopathy in Japan
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Miyuki Hoshi, Eriko Koshimizu, Satoko Miyatake, Naomichi Matsumoto, Atsushi Imamura.
Nội dung
Pages 101-105
16. Reply to the comments on “Spontaneous spinal epidural hematoma mimicking
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Guillain-Barre Syndrome” Hiroshi Yamaguchi, Azusa Maruyama.
Nội dung
Pages 827-828
16. Exclusive affection of the brain in m.4450G>A carriers rather suggests Leigh syndrome than MELAS
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Josef Finsterer.
Nội dung
Page 741
16. Reply to the Letter, “Methotrexate myelopathy: A mimicker of subacute combined degeneration of the spinal cord”
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Takuji Nakamura, Muneaki Matsuo.
Nội dung
Page 646
16. Reply to comments on “The association between brain morphological development and the quality of general movements”
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Tomoki Maeda.
Nội dung
Page 565
16. Reply to “Poor clinico-radiological correlation: A hallmark of acute flaccid myelitis”
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Tác giả
Akihisa Okumura, Harushi Mori.
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Page 482
16. Cover
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Page IBC
16. Facial nerve palsy associated with atomoxetine-induced hypertension
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Hironobu Kobayashi, Katsunori Fujii, Masayo Kobayashi, Naoki Saito, ... Naoki Shimojo.
Nội dung
Pages 310-312
16. An unusual manifestation of Sjögren syndrome encephalitis
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Kenji Iwai, Kiyoko Amo, Ichiro Kuki, Masataka Fukuoka, ... Masao Togawa.
Nội dung
Pages 217-220
16. Elimination of amyloid precursor protein in senile plaques in the brain of a patient with Alzheimer-type dementia and Down syndrome
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Yasuhiro Arai, Yuji Iwasaki, Toshihiro Suzuki, Shuuhei Ide, Makiko Kaga.
Nội dung
Pages 106-110
17. Announcements and reports and Call for Papers
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Nội dung
Page I
17. Announcements and reports and Call for Papers
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Page I
17. Announcements and reports
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Nội dung
Page I
17. Causal connection between methamphetamine and neurotoxicity not established
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Christopher Medina-Kirchner, Ciara A. Torres.
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Page 647
17. Corrigendum to “Measuring in vivo cerebral maturation using age-related T2 relaxation times at 3 T” [Brain Dev. 40 (2018) 85–93]
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Eva Bültmann, Loukia M. Spineli, Hans Hartmann, Heinrich Lanfermann.
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Page 566
17. Announcements and reports
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Nội dung
Page I
17. Contents
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Page OBC
17. Announcements and reports
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Nội dung
Pages I-II
17. Mitochondrial dysfunction in ATP13A2 carriers
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Josef Finsterer, Fulvio A. Scorza, Ana C. Fiorini, Carla A. Scorza, Antonio Carlos de Almeida.
Nội dung
Pages 221-222
17. A case of subacute combined degeneration of the spinal cord due to folic acid and copper deficiency
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Takuji Nakamura, Masanori Nishi, Mihoko Rikitake, Daisuke Koga, ... Muneaki Matsuo.
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Pages 111-115
18. Cover
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Page IBC
18. Cover
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Page IBC
18. Response to “Causal connection between methamphetamine and neurotoxicity not established”
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Eugenia Maranella.
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Page 648
18. Announcements and reports
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Page I
18. Cover
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Page IBC
18. Cover
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Page IBC
18. ATP13A2-related juvenile-onset Parkinson disease
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Jehan Suleiman, Ayman W. El-Hattab.
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Page 223
18. Dense array EEG estimated the epileptic focus in a patient with epilepsy secondary to tuberous sclerosis complex
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Yuki Amano, Ayataka Fujimoto, Tohru Okanishi, Mitsuyo Nishimura, Hideo Enoki.
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Pages 116-120
19. Contents
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Page OBC
19. Contents
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Page OBC
19. Announcements and reports
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Page I
19. Cover
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Page IBC
19. Contents
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19. Contents
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Page OBC
19. Reply to the Letter, “Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation”
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Hitoshi Osaka, Akihiko Miyauchi.
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Page 224
19. Avoid valproate in patients with IARS2 mutations
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Josef Finsterer, Sinda Zarrouk-Mahjoub.
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Page 121
20. Cover
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Page IBC
20. Announcements and reports
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Pages I-II
20. Reply to: Avoid valproate in patients with IARS2 mutations
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Yusuke Takezawa, Hiromi Fujie, Atsuo Kikuchi, Shigeo Kure.
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Page 122
21. Contents
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Page OBC
21. Cover
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Page IBC
21. Announcements and reports
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Pages I-II
22. Cover
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23. Contents
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