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Brain and Development
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Volume 41, Issue 9
Pages 743-828 (October 2019)
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1. Editorial Board
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Page IFC
1. Editorial Board
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Page IFC
2. Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment
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Sachiyo Fukushima, Ichiro Morioka, Shohei Ohyama, Kosuke Nishida, ... Hideto Yamada.
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Pages 743-750
3. Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder
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Yoshihiko Saito, Yoshimi Kaga, Eiji Nakagawa, Mariko Okubo, ... Masumi Inagaki.
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Pages 751-759
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.
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Pages 760-768
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.
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Pages 769-775
6. Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
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Toshiyuki Yamamoto, Taichi Imaizumi, Keiko Yamamoto-Shimojima, Yongping Lu, ... Nobuhiko Okamoto.
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Pages 776-782
7. Phenotypic manifestations between male and female children with CDKL5 mutations
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Jao-Shwann Liang, Hsin Huang, Jinn-Shyan Wang, Jyh-Feng Lu.
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Pages 783-789
8. Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy
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Naomi Hino-Fukuyo, Kazuhiro Haginoya, Toshiyuki Takahashi, Ichiro Nakashima, ... Shigeo Kure.
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Pages 790-795
9. Cumulative jerk as an outcome measure in nonambulatory Duchenne muscular dystrophy
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Tatsuya Fujii, Eri Takeshita, Yasuyuki Iwata, Hiroyuki Yajima, ... Tomohiro Kumada.
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Pages 796-802
10. Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C
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Atsuko Kori, Ikumi Hori, Tatsushi Tanaka, Kohei Aoyama, ... Shinji Saitoh.
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Pages 803-807
11. Usefulness of diagnostic tools in a GLUT1 deficiency syndrome patient with 2 inherited mutations
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Blandine Dozières-Puyravel, Sasha Zaman, Steven Petrou, Laurent François, ... Stéphane Auvin.
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Pages 808-811
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
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.
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Pages 817-819
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
15. Letter to the editor
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Natan Gadoth.
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Page 826
16. Reply to the comments on “Spontaneous spinal epidural hematoma mimicking
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Guillain-Barre Syndrome” Hiroshi Yamaguchi, Azusa Maruyama.
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Pages 827-828
17. Announcements and reports and Call for Papers
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Page I
17. Announcements and reports and Call for Papers
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Page I
18. Cover
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Page IBC
19. Contents
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