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Refinado por: assunto: Neurology remover
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1
Imbalance of interneuron distribution between neocortex and basal ganglia: Consideration of epileptogenesis of focal cortical dysplasia
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Imbalance of interneuron distribution between neocortex and basal ganglia: Consideration of epileptogenesis of focal cortical dysplasia

Sakakibara, T ; Sukigara, S ; Otsuki, T ; Takahashi, A ; Kaneko, Y ; Kaido, T ; Saito, Y ; Sato, N ; Nakagawa, E ; Sugai, K ; Sasaki, M ; Goto, Y ; Itoh, M

Journal of the neurological sciences, 2012-12, Vol.323 (1), p.128-133 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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2
P6: Hemodynamic evaluation of cognitive shifting in children with autism spectrum disorder
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P6: Hemodynamic evaluation of cognitive shifting in children with autism spectrum disorder

Yasumura, A ; Kokubo, N ; Yasumura, Y ; Moriguchi, Y ; Nakagawa, E ; Hiraki, K ; Inagaki, M

Clinical neurophysiology, 2014-06, Vol.125, p.S50-S50 [Periódico revisado por pares]

Elsevier Ireland Ltd

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3
Generation and Characterization of Immortalized Human Microglial Cell Lines: Expression of Cytokines and Chemokines
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Generation and Characterization of Immortalized Human Microglial Cell Lines: Expression of Cytokines and Chemokines

Nagai, A. ; Nakagawa, E. ; Hatori, K. ; Choi, H.B. ; McLarnon, J.G. ; Lee, M.A. ; Kim, S.U.

Neurobiology of disease, 2001-12, Vol.8 (6), p.1057-1068 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Type-specific selectivity pattern of skeletal muscle images in spinal muscular atrophy
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Artigo
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Type-specific selectivity pattern of skeletal muscle images in spinal muscular atrophy

Inoue, M ; Ishiyama, A ; Komaki, H ; Takeshita, E ; Shimizu-Motohashi, Y ; Saito, T ; Nakagawa, E ; Sugai, K ; Minami, N ; Goto, Y ; Sasaki, M

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S194-S194 [Periódico revisado por pares]

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5
Early scoliosis surgery may prevent deterioration of respiratory function in Ullrich congenital muscular dystrophy
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Artigo
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Early scoliosis surgery may prevent deterioration of respiratory function in Ullrich congenital muscular dystrophy

Kohashi, K ; Ishiyama, A ; Takeshita, E ; Shimizu-Motohashi, Y ; Saito, T ; Nakagawa, E ; Komaki, H ; Sugai, K ; Nishino, I ; Saito, W ; Takaso, M ; Sasaki, M

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S264-S265 [Periódico revisado por pares]

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6
G.P.76
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G.P.76

Koichihara, R ; Komaki, H ; Ishiyama, A ; Hayashi, Y.K ; Tsuburaya, R.S ; Saito, T ; Saito, Y ; Nakagawa, E ; Sugai, K ; Sasaki, M ; Nonaka, I ; Nishino, I

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.817-817 [Periódico revisado por pares]

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7
G.P.262
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Artigo
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G.P.262

Okubo, M ; Ishiyama, A ; Komaki, H ; Takeshita, E ; Saito, T ; Saito, Y ; Nakagawa, E ; Sugai, K ; Hayashi, Y.K ; Nishino, I ; Sasaki, M

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.895-895 [Periódico revisado por pares]

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8
C.P.4 Congenital fiber type disproportion with myofibrillar disorganization and altered internal nuclei is caused by RYR1 mutation
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C.P.4 Congenital fiber type disproportion with myofibrillar disorganization and altered internal nuclei is caused by RYR1 mutation

Ishiyama, A ; Hayashi, Y.K ; Kajino, S ; Komaki, H ; Saito, T ; Saito, Y ; Nakagawa, E ; Sugai, K ; Sasaki, M ; Noguchi, S ; Nonaka, I ; Nishino, I

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.842-842 [Periódico revisado por pares]

Elsevier B.V

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9
P4.30 Muscle MRI of spinal muscular atrophy
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Artigo
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P4.30 Muscle MRI of spinal muscular atrophy

Komaki, H ; Sakuma, H ; Saito, Y ; Nakagawa, E ; Sugai, K ; Sasaki, M

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.667-667 [Periódico revisado por pares]

Elsevier B.V

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10
P25-23 Change of interhemispheric synchronized spike on magnetoencephalography before and after total callosotomy
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Artigo
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P25-23 Change of interhemispheric synchronized spike on magnetoencephalography before and after total callosotomy

Sakakibara, T ; Kaneko, Y ; Sugai, K ; Otsuki, T ; Kaido, T ; Takahashi, A ; Nakagawa, E ; Sasaki, M

Clinical neurophysiology, 2010, Vol.121, p.S256-S256 [Periódico revisado por pares]

Elsevier Ireland Ltd

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