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Brain and Development
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Volume 41, Issue 2
Pages 123-224 (February 2019)
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1. Editorial Board
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Nội dung
Page IFC
2. Behavioral profiles in Rett syndrome: Data from the natural history study
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Caroline B. Buchanan, Jennifer L. Stallworth, Alexandra E. Scott, Daniel G. Glaze, ... Walter E. Kaufmann.
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Pages 123-134
3. Combining visual sensory functions and visuospatial orienting functions in children with visual pathology: A longitudinal study
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Marlou J.G. Kooiker, Hélène J.M. Verbunt, Johannes van der Steen, Johan J.M. Pel.
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Pages 135-149
4. Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders
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Ayako Kashimada, Setsuko Hasegawa, Toshihiro Nomura, Hiroshi Shiraku, ... Masatoshi Takagi.
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Pages 150-157
5. Factors associated with electroencephalographic and clinical remission of benign childhood epilepsy with centrotemporal spikes
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Eun Hye Lee, Su-Jeong You.
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Pages 158-162
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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Shinichi Magara, Takao Komatsubara, Moemi Hojo, Yu Kobayashi, ... Jun Tohyama.
Nội dung
Pages 163-172
7. Effects of human umbilical cord blood CD34+ cell transplantation in neonatal hypoxic-ischemia rat model
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Yan Yu, YiZhong Yan, Zhen Luo, Pan Luo, ... LaMei Cheng.
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Pages 173-181
8. Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation
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Mona Entezam, Masoumeh Razipour, Saeed Talebi, Mehran Beiraghi Toosi, Mohammad Keramatipour.
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Pages 182-186
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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Tsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, Kenichiro Hata.
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Pages 187-190
10. Severe neurologic and hepatic toxicity in a newborn prenatally exposed to methamphetamine. A case report
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Eugenia Maranella, Arianna Mareri, Valentina Nardi, Cecilia Di Natale, ... Sandra Di Fabio.
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Pages 191-194
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
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.
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Pages 201-204
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.
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Pages 205-209
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
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
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
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
18. ATP13A2-related juvenile-onset Parkinson disease
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Jehan Suleiman, Ayman W. El-Hattab.
Nội dung
Page 223
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
20. Announcements and reports
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Pages I-II
21. Cover
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Page IBC
