Papers - OHMORI Iori
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A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy Reviewed
Iori Ohmori, Mamoru Ouchida, Takafumi Miki, Nobuyoshi Mimaki, Shigeki Kiyonaka, Teiichi Nishiki, Kazuhito Tomizawa, Yasuo Mori, Hideki Matsui
NEUROBIOLOGY OF DISEASE 32 ( 3 ) 349 - 354 2008.12
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Novel SCN5A Mutations and SNP in Patients with Brugada Syndrome
Kazufumi Nakamura, Daiji Miura, Kaoru Kobayashi, Mamoru Ouchida, Kenji Shimizu, Iori Ohmori, Nobuhiro Nishii, Satoshi Nagase, Hiroshi Morita, Yoshiki Hata, Takefumi Oka, Kengo Kusano, Tohru Ohe
CIRCULATION 118 ( 18 ) S981 - S981 2008.10
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MECP2遺伝子エキソン1およびプロモーター領域に変異をもつレット症候群
大内田 守, 吉永 治美, 大守 伊織, 大塚 頌子, 岡 えい次
脳と発達 40 ( Suppl. ) S288 - S288 2008.5
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A screening test for the prediction of Dravet syndrome before one year of age Reviewed
Junri Hattori, Mamoru Ouchida, Junko Ono, Susumu Miyake, Satoshi Maniwa, Nobuyoshi Mimaki, Yoko Ohtsuka, Iori Ohmori
EPILEPSIA 49 ( 4 ) 626 - 633 2008.4
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Rasmussen encephalitis associated with SCN1A mutation Reviewed
Iori Ohmori, Mamoru Ouchida, Katsuhiro Kobayashi, Yoshimi Jitsumori, Takushi Inoue, Kenji Shimizu, Hideki Matsui, Yoko Ohtsuka, Yoshihiro Maegaki
EPILEPSIA 49 ( 3 ) 521 - 526 2008.3
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Development of bionanocapsules targeting brain tumors Reviewed
Yumi Tsutsui, Kazuhito Tomizawa, Mana Nagita, Hiroyuki Michiue, Tei-ichi Nishiki, Iori Ohmori, Masaharu Seno, Hideki Matsui
JOURNAL OF CONTROLLED RELEASE 122 ( 2 ) 159 - 164 2007.9
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A Cdk5 inhibitor enhances the induction of insulin secretion by exendin-4 both in vitro and in vivo Reviewed
Kohsuke Kitani, Shigeo Oguma, Tei-Ichi Nishiki, Iori Ohmori, Herve Galons, Hideki Matsui, Laurent Meijer, Kazuhito Tomizawa
JOURNAL OF PHYSIOLOGICAL SCIENCES 57 ( 4 ) 235 - 239 2007.8
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Truncations of amphiphysin I by calpain inhibit vesicle endocytosis during neural hyperexcitation Reviewed
Yumei Wu, Shuang Liang, Yoshiya Oda, Iori Ohmori, Tei-Ichi Nishiki, Kohji Takei, Hideki Matsui, Kazuhito Tomizawa
EMBO JOURNAL 26 ( 12 ) 2981 - 2990 2007.6
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服部 旬里, 御牧 信義, 大守 伊織, 大野 順子, 大内田 守, 大塚 頌子
脳と発達 39 ( Suppl. ) S154 - S154 2007.6
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Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy Reviewed
Iori Ohmori, Kristopher M. Kahlig, Thomas H. Rhodes, Dao W. Wang, Alfred L. George
EPILEPSIA 47 ( 10 ) 1636 - 1642 2006.10
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Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures Reviewed
TH Rhodes, CG Vanoye, Ohmori, I, Ogiwara, I, K Yamakawa, AL George
JOURNAL OF PHYSIOLOGY-LONDON 569 ( 2 ) 433 - 445 2005.12
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Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures Reviewed
M Ito, Ohmori, I, T Nakahori, M Ouchida, Y Ohtsuka
NEUROSCIENCE LETTERS 383 ( 3 ) 220 - 224 2005.8
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Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms Reviewed
T Fukuda, Y Yamashita, S Nagamitsu, K Miyamoto, JJ Jin, I Ohmori, Y Ohtsuka, K Kuwajima, S Endo, T Iwai, H Yamagata, Y Tabara, T Miki, T Matsuishi, Kondo, I
BRAIN & DEVELOPMENT 27 ( 3 ) 211 - 217 2005.4
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Relationship between severity of epilepsy and developmental outcome in Angelman syndrome Reviewed
Y Ohtsuka, K Kobayashi, H Yoshinaga, T Ogino, I Ohmori, K Ogawa, E Oka
BRAIN & DEVELOPMENT 27 ( 2 ) 95 - 100 2005.3
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Relation between typical and borderline severe myoclonic epilepsy in infancy. Reviewed
Y Ohtsuka, Ohmori, I, T Ogino, K Kobayashi, E Oka
EPILEPSIA 46 11 - 12 2005
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EEG in childhood absence epilepsy Reviewed
H Yoshinaga, Y Ohtsuka, K Tamai, Tamura, I, M Ito, Ohmori, I, E Oka
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY 13 ( 5 ) 296 - 302 2004.7
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Clinical and electroencephalographic characteristics of children with febrile seizures plus Reviewed
K Kobayashi, Y Ohtsuka, I Ohmori, Y Nishio, M Fujiwara, M Ito, E Oka
BRAIN & DEVELOPMENT 26 ( 4 ) 262 - 268 2004.6
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Initiation of treatment and selection of antiepileptic drugs in childhood epilepsy Reviewed
E Oka, T Murakami, T Ogino, T Kobayashi, Ohmori, I, T Akiyama, M Ito
EPILEPSIA 45 17 - 19 2004
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Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations? Reviewed
Ohmori, I, Y Ohtsukaa, M Ouchida, T Ogino, S Maniwa, K Shimizu, E Oka
BRAIN & DEVELOPMENT 25 ( 7 ) 488 - 493 2003.10
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Paroxysmal movement disorders in severe myoclonic epilepsy in infancy Reviewed
Y Ohtsuka, Ohmori, I, T Ogino, M Ouchida, K Shimizu, E Oka
BRAIN & DEVELOPMENT 25 ( 6 ) 401 - 405 2003.9