Anti-NMDAR autoimmune encephalitis (English)
- New search for: Miya, K.
- New search for: Takahashi, Y.
- New search for: Mori, H.
- New search for: Miya, K.
- New search for: Takahashi, Y.
- New search for: Mori, H.
In:
BRAIN AND DEVELOPMENT -INTERNATIONAL EDITION-
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36
, 8
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645-652
;
2014
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ISSN:
- Article (Journal) / Print
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Title:Anti-NMDAR autoimmune encephalitis
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Contributors:
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Published in:BRAIN AND DEVELOPMENT -INTERNATIONAL EDITION- ; 36, 8 ; 645-652
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam.
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Publication date:2014-01-01
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Size:8 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 612.82
- Further information on Dewey Decimal Classification
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Classification:
DDC: 612.82 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 36, Issue 8
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 645
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Anti-NMDAR autoimmune encephalitisMiya, K. / Takahashi, Y. / Mori, H. et al. | 2014
- 653
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Dibutyl phthalate-induced neurotoxicity in the brain of immature and mature rat offspringLi, X. / Jiang, L. / Cheng, L. / Chen, H. et al. | 2014
- 661
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Disruption of Aspm causes microcephaly with abnormal neuronal differentiationFujimori, A. / Itoh, K. / Goto, S. / Hirakawa, H. / Wang, B. / Kokubo, T. / Kito, S. / Tsukamoto, S. / Fushiki, S. et al. | 2014
- 670
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Serum tau protein level serves as a predictive factor for neurological prognosis in neonatal asphyxiaTakahashi, K. / Hasegawa, S. / Maeba, S. / Fukunaga, S. / Motoyama, M. / Hamano, H. / Ichiyama, T. et al. | 2014
- 676
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Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutationsXu, X. / Zhang, Y. / Sun, H. / Liu, X. / Yang, X. / Xiong, H. / Jiang, Y. / Bao, X. / Wang, S. / Yang, Z. et al. | 2014
- 682
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Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agentsVantaggiato, C. / Cantoni, O. / Guidarelli, A. / Romaniello, R. / Citterio, A. / Arrigoni, F. / Doneda, C. / Castelli, M. / Airoldi, G. / Bresolin, N. et al. | 2014
- 690
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Pseudotumor cerebri/idiopathic intracranial hypertension in children: An experience of a tertiary care hospitalDeğerliyurt, A. / Teber, S. / Karakaya, G. l. / Güven, A. / Şeker, E. D. / Arhan, E. P. / Şayli, T. l. et al. | 2014
- 700
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Psychometric properties of Japanese version of the Swanson, Nolan, and Pelham, version-IV Scale-Teacher Form: A study of school children in community samplesInoue, Y. / Ito, K. / Kita, Y. / Inagaki, M. / Kaga, M. / Swanson, J. M. et al. | 2014
- 707
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An autopsy case of microencephaly, bizarre putaminal lesion, and cerebellar atrophy with heart and liver diseasesOkoshi, Y. / Hayashi, M. / Kanda, S. / Yamamoto, T. et al. | 2014
- 711
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Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutationMagnin, E. / Blagosklonov, O. / Sylvestre, G. / Minot, D. / Thevenon, J. / Faivre, L. / Boulahdour, H. / Thauvin-Robinet, C. / Rumbach, L. et al. | 2014
- 716
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Delayed myelination is not a constant feature of Allan–Herndon–Dudley syndrome: Report of a new case and review of the literatureAzzolini, S. / Nosadini, M. / Balzarin, M. / Sartori, S. / Suppiej, A. / Mardari, R. / Greggio, N. A. / Toldo, I. et al. | 2014
- 721
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A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese childSaida, K. / Inaba, Y. / Hirano, M. / Satake, W. / Toda, T. / Suzuki, Y. / Sudo, A. / Noda, S. / Hidaka, Y. / Hirabayashi, K. et al. | 2014
- 725
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A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndromeKumakura, A. / Takahashi, S. / Okajima, K. / Hata, D. et al. | 2014
- 730
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Leigh syndrome with Fukuyama congenital muscular dystrophy: A case reportKondo, H. / Tanda, K. / Tabata, C. / Hayashi, K. / Kihara, M. / Kizaki, Z. / Taniguchi-Ikeda, M. / Mori, M. / Murayama, K. / Ohtake, A. et al. | 2014
- 734
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A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorderKim, S. H. / Lee, J. S. / Lim, B. C. / Kim, K. J. / Hwang, Y. S. / Park, J. D. / Cheon, J. E. / Kim, I. O. / Kim, B. N. / Chae, J. H. et al. | 2014
- I
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Announcements and Reports| 2014
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Contents| 2014
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Editorial Board| 2014
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Cover| 2014
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Call for Papers| 2014