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Brain and Development
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Volume 41, Issue 5
Pages 397-482 (May 2019)
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1. Editorial Board
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Page IFC
2. Catch-up growth and behavioral development among preterm, small-for-gestational-age children: A nationwide Japanese population-based study
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Tác giả
Akihito Takeuchi, Takashi Yorifuji, Mariko Hattori, Kei Tamai, ... Hiroyuki Doi.
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Pages 397-405
3. Nutritional status among women whose pregnancy outcome was afflicted with neural tube defects in Tigray region of Ethiopia
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Abadi Leul Welderufael, Birhane Alem Berihu, Yibrah Berhe, Tony Magana, ... Afework Mulugeta.
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Pages 406-412
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
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.
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Pages 420-427
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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Shih-Yun Lan, Cheng-Yen Kuo, Cheng-Che Chou, Shu-Sing Kong, ... Kuang-Lin Lin.
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Pages 428-435
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
8. Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan
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Akihisa Okumura, Harushi Mori, Pin Fee Chong, Ryutaro Kira, ... Keiko Tanaka-Taya.
Nội dung
Pages 443-451
9. Phenotypic features of 1q41q42 microdeletion including WDR26 and FBXO28 are clinically recognizable: The first case from Japan
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Tomoe Yanagishita, Keiko Yamamoto-Shimojima, Sayaka Nakano, Testuya Sasaki, ... Toshiyuki Yamamoto.
Nội dung
Pages 452-455
10. Electroencephalographic and epilepsy findings in mecp2 duplication syndrome. A family study
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Federica Lotti, Ursula Geronzi, Salvatore Grosso.
Nội dung
Pages 456-459
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
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
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.
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Pages 470-473
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
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
16. Reply to “Poor clinico-radiological correlation: A hallmark of acute flaccid myelitis”
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Akihisa Okumura, Harushi Mori.
Nội dung
Page 482
17. Announcements and reports
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Page I
18. Cover
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Page IBC
19. Contents
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Page OBC