Changes in negative and positive EEG shifts during slow cortical potential training in children with attention-deficit/hyperactivity disorder: a preliminary investigationTAKAHASHI, Junichi; YASUMURA, Akira; NAKAGAWA, Eiji et al.Neuroreport (Oxford). 2014, Vol 25, Num 8, pp 618-624, issn 0959-4965, 7 p.Article

Fabrication and characterization of electro-phosphorescent organic light-emitting devices with a ferromagnetic cathode for observation of spin injection effectSHIKOH, Eiji; NAKAGAWA, Eiji; FUJIWARA, Akihiko et al.Synthetic metals. 2010, Vol 160, Num 3-4, pp 230-234, issn 0379-6779, 5 p.Conference Paper

Novel pathological abnormalities of deep brain structures including dysplastic neurons in anterior striatum associated with focal cortical dysplasia in epilepsyKAIDO, Takanobu; OTSUKI, Taisuke; HONDA, Ryoko et al.Journal of neurosurgery. Pediatrics. 2012, Vol 10, Num 3, pp 217-225, issn 1933-0707, 9 p.Article

Repeat magnetoencephalography and surgeries to eliminate atonic seizures of non-lesional frontal lobe epilepsyNAKAYAMA, Tojo; OTSUKI, Taisuke; KANEKO, Yu et al.Epilepsy research. 2009, Vol 84, Num 2-3, pp 263-267, issn 0920-1211, 5 p.Article

TULIP1 (RALGAPA1 ) haploinsufficiency with brain development delaySHIMOJIMA, Keiko; KOMOIKE, Yuta; OSAWA, Makiko et al.Genomics (San Diego, Calif.). 2009, Vol 94, Num 6, pp 414-422, issn 0888-7543, 9 p.Article

Reversible altered consciousness with brain atrophy caused by valproic acidYAMANOUCHI, Hideo; OTA, Takako; IMATAKA, George et al.Pediatric neurology. 2003, Vol 28, Num 5, pp 382-384, issn 0887-8994, 3 p.Article

Importance of CAG repeat length in childhood-onset dentatorubral―pallidoluysian atrophyMARUYAMA, Shinsuke; SAITO, Yoshiaki; MINAMI, Narihiro et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2329-2334, issn 0340-5354, 6 p.Article

A Loss-of-Function Mutation in the FTSJ1 Gene Causes Nonsyndromic X-Linked Mental Retardation in a Japanese FamilyTAKANO, Kyoko; NAKAGAWA, Eiji; INOUE, Ken et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 4, pp 479-484, issn 1552-4841, 6 p.Article

Erythropoietin and erythropoietin receptors in human CNS neurons, astrocytes, microglia, and oligodendrocytes grown in cultureNAGAI, Atsushi; NAKAGAWA, Eiji; CHOI, Hyun B et al.Journal of neuropathology and experimental neurology. 2001, Vol 60, Num 4, pp 386-392, issn 0022-3069Article

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutationTAKESHITA, Eri; SAITO, Yoshiaki; GOTO, Yu-Ichi et al.Journal of the neurological sciences. 2011, Vol 308, Num 1-2, pp 168-172, issn 0022-510X, 5 p.Article

Reassessment of phenytoin for treatment of late stage progressive myoclonus epilepsy complicated with status epilepticusMIYAHARA, Ayako; SAITO, Yoshiaki; SUGAI, Kenji et al.Epilepsy research. 2009, Vol 84, Num 2-3, pp 201-209, issn 0920-1211, 9 p.Article

Treatment of epilepsy in severely disabled children with bilateral brain malformationsSAITO, Yoshiaki; SUGAI, Kenji; OTSUKI, Taisuke et al.Journal of the neurological sciences. 2009, Vol 277, Num 1-2, pp 37-49, issn 0022-510X, 13 p.Article

A de novo Direct Duplication of 16q22.1 → q23.1 in a Boy With Midface Hypoplasia and Mental RetardationTOKUTOMI, Tomoharu; WADA, Takahito; NAKAGAWA, Eiji et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 11, pp 2560-2563, issn 1552-4825, 4 p.Article

Delayed Maturation and Differentiation of Neurons in Focal Cortical Dysplasia With the Transmantle Sign: Analysis of Layer-Specific Marker ExpressionSAKAKIBARA, Takafumi; SUKIGARA, Sayuri; NAKAGAWA, Eiji et al.Journal of neuropathology and experimental neurology. 2012, Vol 71, Num 8, pp 741-749, issn 0022-3069, 9 p.Article

The Incidence of Hypoplasia of the Corpus Callosum in Patients With dup (X)[q28] Involving MECP2 Is Associated With the Location of Distal BreakpointsHONDA, Shozo; HAYASHI, Shin; NAKAGAWA, Eiji et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 6, pp 1292-1303, issn 1552-4825, 12 p.Article

Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophyNONODA, Yutaka; SAITO, Yoshiaki; GOTO, Yu-Ichi et al.Journal of the neurological sciences. 2009, Vol 287, Num 1-2, pp 52-59, issn 0022-510X, 8 p.Article

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndromeNAKAMURA, Kazuyuki; KATO, Mitsuhiro; IMAI, Katsumi et al.Neurology. 2013, Vol 81, Num 11, pp 992-998, issn 0028-3878, 7 p.Article

Abnormal maturation and differentiation of neocortical neurons in epileptogenic cortical malformation: Unique distribution of layer-specific marker cells of focal cortical dysplasia and hemimegalencephalyARAI, Asako; SAITO, Takashi; SAITO, Yuko et al.Brain research. 2012, Vol 1470, pp 89-97, issn 0006-8993, 9 p.Article

Effects of acetazolamide on epileptic apnea in migrating partial seizures in infancyIRAHARA, Kaori; SAITO, Yoshiaki; SUGAI, Kenji et al.Epilepsy research. 2011, Vol 96, Num 1-2, pp 185-189, issn 0920-1211, 5 p.Article

Bromoderma in a patient with migrating partial seizures in infancyNABATAME, Shin; SAITO, Yoshiaki; SAKUMA, Hiroshi et al.Epilepsy research. 2010, Vol 91, Num 2-3, pp 283-288, issn 0920-1211, 6 p.Article

Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancySAKAKIBARA, Takafumi; NAKAGAWA, Eiji; SAITO, Yoshiaki et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 9, pp 2158-2162, issn 0013-9580, 5 p.Article

Startle epilepsy associated with gait-induced seizures: Pathomechanism analysis using EEG, MEG, and PET studiesSAEKI, Keisuke; SAITO, Yoshiaki; SUGAI, Kenji et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 5, pp 1274-1279, issn 0013-9580, 6 p.Article

19.8 GBytes ROM disc readout using a 0.7 NA single objective lens and a violet laser diodeKONDO, Tetsuya; HAYAMI, Atsushi; OKI, Tsuyoshi et al.SPIE proceedings series. 2000, pp 36-42, isbn 0-8194-3733-6Conference Paper