61 - 80 of about 137
English: Imamichi Y, Sekiguchi T, Kitano T, Kajitani T, Okada R, Inaoka Y, Miyamoto K, Uwada J, Takahashi S, Nemoto T, Mano A, Khan MRI, Islam MT, Yuhki KI, Kashiwagi H, Ushikubi F, Suzuki N, Taniguchi T, Yazawa T, Diethylstilbestrol administration 1 inhibits theca cell androgen and granulosa cell estrogen production in immature rat ovary. , Sci Rep , vol.7 (p.8374 - ) , 2017 , (IF:4.259)
English: Okano S, Tanaka R, Okayama A, Tsuchida E, Nohara F, Suzuki N, Okamoto T, Nagaya K, Takahashi S, Azuma H, Congenital basal meningoceles with different outcomes: a case series , J Med Case Reports , vol.11 (p.359 - ) , 2017
English: Tanaka R, Takahashi S, Okano S, Okayama A, Suzuki N, Kure S, Azuma H, Evolution into moyamoya disease in an infant with internal carotid artery aneurysms , eNeurologicalSci , vol.6 (p.80 - 82) , 2017
English: Fujii T, Ito Y, Takahashi S, Shimono K, Natsume J, Yanagihara K, Oguni H, Outcome of ketogenic diet for GLUT1 deficiency syndrome in Japan: nationwide survey , Brain Dev , vol.38 (p.628 - 637) , 2016 , (IF:1.88)
English: Takahashi S, Tanaka R, Okano S, Okayama A, Suzuki N, Azuma H, Reduced efficacy of enzyme replacement therapy in a child with late-onset Pompe disease. , Pediat Therapeut , vol.6 (2) , 2016
English: Araki A, Ikegami M, Okayama A, Matsumoto N, Takahashi S, Azuma H, Takahashi M, Improved prefrontal activity in ADHD children treated with atomoxetine: a NIRS study , Brain Dev , vol.37 (p.76 - 67) , 2015 , (IF:2.119)
English: Takahashi S, Tanaka R, Okano S, Suzuki N, Okayama A, Azuma H, Characterization of intragenic tandem duplication in the PAFAH1B1 gene leading to isolated lissencephaly sequence , Mol Cytogenet , vol.8 (p.84 - ) , 2015 , (IF:2.14)
English: Takahashi S, Yamamoto S, Okayama A, Araki A, Saitsu H, Matsumoto N, Azuma H, Electroclinical features of epileptic encephalopathy caused by SCN8A mutation , Pediatr Int , vol.57 (p.758 - 762) , 2015 , (IF:0.731)
English: Yamamoto S, Takahashi S, Tanaka R, Okayama A, Araki A, Katano H, Tanaka-Taya K, Azuma H, Human herpesvirus-6 infection-associated acute encephalopathy without skin rash. , Brain Dev , vol.37 (p.829 - 832) , 2015 , (IF:1.542)
English: Ito Y, Takahashi S, Shimono K, Natsume J, Yanagihara K, Fujii T, Oguni H, Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan. , Brain Dev , vol.37 (p.780 - 789) , 2015 , (IF:1.542)
English: Takahashi S, Yamamoto S, Tanaka R, Okayama A, Araki A, Azuma H, Focal frontal epileptiform discharges in a patient with eyelid myoclonia and absence seizures. , Epilepsy Behavior Case Reports , vol.4 (p.35 - 37) , 2015
English: Ohba C, Kato M, Takahashi S, Terashima H, Kubota M, Matsufuji M, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Goldberg-Stern H, Straussberg R, Marom D, Nakashima M, Nishiyama K, Tsurusaki Y, Miyake N, Tanaka F, Matsumoto N, Saitsu H, Early onset epileptic encephalopathy caused by de novo SCN8A mutations , Epilepsia , vol.55 (p.994 - 1000) , 2014 , (IF:3.909)
English: Takahashi S, Yamamoto S, Tanaka R, Okayama A, Araki A, Kajino H, Azuma H, A novel mutation of the SCN4A gene in a Japanese family with paramyotonia congenita. , J Neurol Neurophysiol , vol.5 (p.233 - ) , 2014
English: Utreras E, Hamada R, Prochazkova M, Terse A, Takahashi S, Ohshima T, Kulkarni AB, Suppression of neuroinflammation in forebrain-specific Cdk5 conditional knockout mice by PPAR-gamma agonist improves neuronal loss and early lethality , J Neuroinflammation , vol.11 (p.28 - ) , 2014 , (IF:4.35)
English: Matsumoto N, Takahashi S, Okayama A, Araki A, Azuma H, Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case report , J Med Case Reports , vol.8 (p.174 - ) , 2014 , (IF:0.36)
English: Yoneda Y, Haginoya K, Kato M, Osaka H, Yokochi K, Arai H, Kakita A, Yamamoto T, Otsuki Y, Shimizu S, Wada T, Koyama K, Mino Y, Kondo N, Takahashi S, Hirabayashi S, Takanashi J, Okumura A, Kumagai T, Hirai S, Nabetani M, Saitoh S, Hattori A, Yamasaki M, Kumakura A, Sugo Y, Nishiyama K, Miyatake S, Tsurusaki Y, Doi H, Miyake N, Matsumoto N, Saitsu H, Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly , Ann Neurol , vol.73 (p.48 - 57) , 2013 , (IF:11.089)
English: Hara M, Nishi Y, Yamashita Y, Hirata R, Takahashi S, Nagamitsu S, Hosoda H, Kangawa K, Kojima M, Matsuishi, T, Relation between circulating levels of GH, IGF-1, ghrelin and somatic growth in Rett Syndrome , Brain Dev , vol.36 (p.794 - 800) , 2013 , (IF:2.119)
English: Shiohama T, Fujii K, Takahashi S, Nakamura F, Kohno Y, Reversible t2 prolongations appear in the energy deprivation period in glucose transporter 1 deficiency syndrome , Pediatr Neurol , vol.49 (p.493 - 496) , 2013 , (IF:1.416)
English: Kumakura A, Takahashi S, Okajima K, Hata D, A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome , Brain Dev , vol.36 (p.725 - 729) , 2013 , (IF:2.119)
English: Takahashi S, Matsumoto N, Okayama A, Suzuki N, Araki A, Okajima K, Tanaka H, Miyamoto A, FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome , Clin Genet , vol.82 (p.569 - 573) , 2012 , (IF:3.128)
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