• 研究・業績紹介
  • 脳神経小児科の研究・業績を紹介いたします。

研究業績(平成12年)

  • Kyoiti Ohtan, Kenzo Takeshita. Consideration on the methology of a simple and effective birth defect monitoring system. Cong Anom 40: 2000
  • Koichi Kusuhara, Yuka Sasaki, Futoshi Nakao, Kenji Ihara, Hideji Hattori, Sumimasa Yamashita, Kenji Nihei, Nobuo Koide, Hideo Aiba, Kenzo Takeshita, Toshiro Hara. Analysis of measles virus binding sites of the CD46 gene in patients with subacute sclerosing panencephalitis. J Infectious Disease 181:1447-9:2000
  • Toshiro Hara, Sumimasa Yamashita, Hideo Aiba, Kenji Nihei, Nobuo Koide, Robert A Good, Kenzo Takeshita. Measles virus-specific T helper 1/T helper 2-cytokine production in subacute sclerosing panencephalitis. J NeuroVirologt 6;121-6:2000
  • Y. Kurachi, A. Oka, Y. Ohkoshi, M. Sasaki, M. Itoh, M. Mizuguchi, S. Takashima. Rapid diagnosis of classical late-infantile neuronal ceroid-lipofuscinosis (CLN2) using antibodies against CLN2 protein. Neurology 54;1767-1680:2000
  • H. Yamanouchi, M. Mizuguchi, A. Oka, S. Takashima, L. E. Becker, M. Eguchi, Y. Nakazato. Enhanced GAP-43 expression in cortical dysplasia. NeuroReport 11;1815-1819: 2000
  • Y. Saito, M. Mizuguchi, A. Oka, S. Takashima. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain. Ann Neurol 47;756-764:2000
  • A. Oka, S. Takashima, M. Abe, R. Araki, K. Takeshita. Expression of DNA-dependent protein kinase catalytic subunit and Ku80 in developing human brains: implication of DNA-repair in neurogenesis. Neurosci Lett 292;167-170:2000
  • Y. Saito, A. Oka, M. Mizuguchi, K. Motonaga, Y. Mori, LE Becker, K. Arima, J. Miyauchi, S. Takashima. The development and aging changes of Down's syndrome cell adhesion molecule expression in normal and Down's syndrome brains. Acta Neuropathol(Berl) 100(6);654-64:2000
  • Akaboshi S, Takeshita K. A case of atypical absence seizures induced by leuprolide acetate. Pediatr Neurol 23(3);266-8:2000
  • Akaboshi S, Yoshimura M, Hara T, Kageyama H, Nishikwa K, Kawakami T, Ieshima A, Takeshita K. A case of Hoyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs. Neuropediatrics 31(3);141-4:2000
  • Kato M, Nanba E, Akaboshi S, Shiihara T, Ito A, Honma T, Tsuburaya K, Hayasaka K. Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly. Ann Neurol 47(4);514-6: 2000
  • Itoh M, Suzuki Y, Akaboshi S, Zhang Z, Miyabara S, Takashima S. Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome.Brain Res 858(1);40-7:2000
  • Akaboshi S, Inoue Y, Kubota N, Takeshita K. Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion. Psychiatry Clin Neurosci 54(3);379-80:2000
  • Maegaki Y., Akaboshi S., Inagaki M., Takeshita K. Unilateral involuntary movement associated with streptococcal infection: neurophysiological investigation. Neuropediatrics 31(2);70-4:2000
  • Maegaki Y., Najm I., Terada K., Morris HH., Bingerman WE., Kohaya N., Takenobu A., Kadonaga Y., Lüders HO. Somatosensory evoked high-frequency oscillations recorded directly from the human cerebral cortex. Clin Neurophysiol. 111(11);1916-26:2000
  • Makoto Ueno, Ryutaro Kira, Toshio Matsushima, Takuya Inoue, Masashi Fukui, Kenjiro Gondo, Kenji Ihara, and Toshiro Hara. Moyamoya disease and transforming growth factor-beta1. J Neurosurg 92(5);907-8:2000
  • Makoto Ueno, Youichi Tokunaga, Shinichi Terachi, Kenji Gondo, and Toshiro Hara. Asymmetric sweating in a child with multiple sclerosis. Pediatr Neurol 23(1);74-6:2000
  • Takehiko Inoue, Ryutaro Kira, Yoshitsugu Kaku, Kazuyuki Ikeda, Kenjiro Gondo, Toshiro Hara. Renal tubular acidosis associated with zonisamide therapy. Epilepsia 41(12);1642-4:2000
  • Judy R. Pipo, Toshiyuki Yamamoto, Hiromasa Takeda, Shinji Maegawa, Eiji Nanba, Haruaki Ninomiya, Kousaku Ohno, Kenzo Takeshita. Two novel serine repeat length polymorphisms (codon 1043 ins S and SS) at exon 23 of TSC1 gene. Hum Mut 16(4);375:2000
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