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Genetic analyses and generation of genetic engineered animals for childhood epilepsy focusing on ion channel abnormalities

Research Project

Project/Area Number 18209035
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionFukuoka University

Principal Investigator

HIROSE Shinichi  Fukuoka University, 医学部, 教授 (60248515)

Co-Investigator(Kenkyū-buntansha) 三角 佳生  福岡大学, 医学部, 准教授 (10148877)
上原 明  福岡大学, 医学部, 准教授 (60140745)
荒木 喜美  熊本大学, 学内共同利用施設, 准教授 (90211705)
斎藤 亮  福岡大学, 薬学部, 講師 (80122696)
高野 行夫  福岡大学, 薬学部, 教授 (50113246)
Co-Investigator(Renkei-kenkyūsha) MISUMI Yoshio  福岡大学, 医学部, 准教授 (10148877)
UEHARA Akira  福岡大学, 医学部, 准教授 (60140745)
ARAKI Kimi  熊本大学, 学内共同利用施設, 准教授 (90211705)
SAITO Ryo  福岡大学, 薬学部, 講師 (80122696)
TAKANO Yukio  福岡大学, 薬学部, 教授 (50113246)
DESHIMARU Masanobu  福岡大学, 理学部, 准教授 (70309889)
Project Period (FY) 2006 – 2008
Project Status Completed (Fiscal Year 2008)
Budget Amount *help
¥43,160,000 (Direct Cost: ¥33,200,000、Indirect Cost: ¥9,960,000)
Fiscal Year 2008: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Fiscal Year 2007: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Fiscal Year 2006: ¥29,900,000 (Direct Cost: ¥23,000,000、Indirect Cost: ¥6,900,000)
Keywords小児神経学 / チャネル / 受容体 / てんかん / 中枢神経 / 遺伝子
Research Abstract

設立・管理するてんかん遺伝子バンクを利用し、脳に発現するイオンチャネルに的を絞り、遺伝子変異をスクリーニングし、あわせて発見された変異チャネルの電気生理学的異常をex vivoで検証する。
さらにヒトで発見されたチャネル変異を持つてんかんモデル動物を作出し、チャネルの異常がてんかんの発症へとつながる過程を明らかにし、てんかんの分子病態をin vivoで明らかにする。

Report

(5 results)
  • 2008 Annual Research Report   Self-evaluation Report ( PDF )   Final Research Report ( PDF )
  • 2007 Annual Research Report
  • 2006 Annual Research Report
  • Research Products

    (88 results)

All 2009 2008 2007 2006

All Journal Article (54 results) (of which Peer Reviewed: 29 results) Presentation (30 results) Patent(Industrial Property Rights) (4 results)

  • [Journal Article] de novo KCNQ2 mutation detected innon-familial benign neonatal convulsions2009

    • Author(s)
      Ishii A, Fukuma G, Uehara A, Miyajima T, MakitaY, Hamachi A, Yasukochi M, Inoue T, Yasumoto S,Okada M, Kaneko S, Mitsudome A, Hirose S
    • Journal Title

      BrainDev 31(1)

      Pages: 27-33

    • Related Report
      2008 Self-evaluation Report
  • [Journal Article] Lack of potassiumcurrent in W309R mutant KCNQ3 channelcausing benign familial neonatalconvulsions (BFNC)2009

    • Author(s)
      Sugiura Y, Nakatsu F, Hiroyasu K, Ishii A, Hirose S, Okada M, Jibiki I, Ohno H,Kaneko S, Ugawa Y
    • Journal Title

      Epilepsy Res 84(1)

      Pages: 82-5

    • Related Report
      2008 Self-evaluation Report
  • [Journal Article] Developmental changes in KCNQ2 and KCNQ3 expression in human brain : possible contribution to the age-dependent etiology of benign familial neonatal convulsions2008

    • Author(s)
      Kanaumi T, Takashima S, Iwasaki H, Itoh M, Mitsudome A, Hirose S.
    • Journal Title

      Brain Dev 30(5)

      Pages: 0-0

    • NAID

      10025577003

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Progress in genetics of severe myoclonic epilepsy in fancy2008

    • Author(s)
      Kurahashi K, Wang J, Ishii A, Fukuma G, Hamachi A, Yonetani M, Ogawa A, Ohfu M, Inoue T, Yasumoto S, Hirose S.
    • Journal Title

      Progress in Epileptic Disorders(In: Fukuyama Y, Takahashi T, editors. Biology of Seizere Susceptibility in Developing Brain. Paris: Editions John Libbey Eurotext Montrouge)

      Pages: 1-3

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] High-Grade mature B-cell lymphoma with Burkitt-like morphology : Results of a clinicopathological study of 72 Japanese patients2008

    • Author(s)
      Nomura Y, Karube K, Suzuki R, Guo Ying, Takeshita M, Hirose S, Nakamura S, Yoshida T, Kikuchi M, Ohshima K.
    • Journal Title

      Cancer Sciense 99(2)

      Pages: 246-52

    • NAID

      10024002025

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Altered KCNQ3 potassium channel function caused by the W309R pore-helix mutation found in human epilepsy2008

    • Author(s)
      Uehara A, Nakamura Y, Shioya T, Hirose S, Yasukochi M, Uehara K.
    • Journal Title

      J Membr Biol 222(2)

      Pages: 55-63

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy2008

    • Author(s)
      Wang JW, Kurahashi H, Ishii A, Kojima T, Ohfu M, Inoue T, Ogawa A, Yasumoto S, Oguni H, Kure 5, Fujii T, Ito M, Okuno T, Shirasaka Y, Natsume J, Hasegawa A, Konagaya A, Kaneko S, Hirose S.
    • Journal Title

      Epilepsia 49(9)

      Pages: 1528-34

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Rats Harboring S284L Chrna4 Mutation Show Attenuation of Synaptic and Extrasynaptic GABAergic Transmission and Exhibit the Nocturnal Frontal Lobe Epilepsy Phenotype2008

    • Author(s)
      Zhu G, Okada M, Yoshida S, Ueno S, Mori F, Takahara T, Saito R, Miura Y, Kishi A, Tomiyama M, Sato A, Kojima T, Fukuma G, Wakabayashi K, Hase K, Ohno H, Kijima H, Takano Y, Mitsudome A, Kaneko S, Hirose S.
    • Journal Title

      J Neurosci 28(47)

      Pages: 12465-76

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Microchromosomal deletions involvingSCN1A and adjacent genes in severe myoclonicepilepsy in infancy2008

    • Author(s)
      Wang JW, Kurahashi H, Ishii A, Kojima T, OhfuM, Inoue T, Ogawa A, Yasumoto S, Oguni H,Kure S, Fujii T, Ito M, Okuno T, Shirasaka Y,Natsume J, Hasegawa A, Konagaya A, Kaneko S,Hirose S
    • Journal Title

      Epilepsia 49(9)

      Pages: 1528-34

    • Related Report
      2008 Self-evaluation Report
  • [Journal Article] Rats Harboring S284LChrna4 Mutation Show Attenuation of Synapticand Extrasynaptic GABAergic Transmission and Exhibit the Nocturnal Frontal Lobe Epilepsy Phenotype2008

    • Author(s)
      Zhu G, Okada M, Yoshida S, Ueno S, Mori F, Takahara T, Saito R, Miura Y, Kishi A, TomiyamaM, Sato A, Kojima T, Fukuma G, Wakabayashi K,Hase K, Ohno H, Kijima H, Takano Y, MitsudomeA, Kaneko S, Hirose S
    • Journal Title

      J Neurosci 28(47)

      Pages: 12465-76

    • Related Report
      2008 Self-evaluation Report
  • [Journal Article] Developmental changes in KCNQ2 and KCNQ3 expression in humanbrain : possible contribution to the age-dependent etiology of benign familial neonatal convulsions2008

    • Author(s)
      Hirose S., et al
    • Journal Title

      Brain Dev 30(5)

      Pages: 362-9

    • NAID

      10025577003

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy.2008

    • Author(s)
      Hirose S., et al
    • Journal Title

      Epilepsia 49(9)

      Pages: 1528-9

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Rats Harboring S284L Chrna4 Mutation Show Attenuation of Synaptic and Extrasynaptic GABAergic Transmission and Exhibit the Nocturnal Frontal Lobe Epilepsy Phenotype.2008

    • Author(s)
      Hirose S., et al
    • Journal Title

      J Neurosci 28(47)

      Pages: 12465-76

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Altered KCNQ3 potassium channel function caused by the W309R pore-helix mutation found in human epilepsy.2008

    • Author(s)
      Hirose S., et al
    • Journal Title

      J Membr Biol 222(2)

      Pages: 55-63

    • Related Report
      2008 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Mutation screening of AP3M2 in Japanese epilepsy patients2007

    • Author(s)
      Huang MC, Okada M, Nakatsu F, Oguni H, Ito M, Morita K, Nagafuji H, Hirose S, Sakaki Y, Kaneko S, Ohno H, Kojima T.
    • Journal Title

      Brain Dev 29(8)

      Pages: 462-7

    • NAID

      10024136602

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Sympathetic skin response in patients with severe motor and intellectual disabilities2007

    • Author(s)
      Ogawa A, Hamamoto K, Hirose S, Fujikawa M, Mitsudome A.
    • Journal Title

      No To Hattatsu 39(5)

      Pages: 347-50

    • NAID

      10019813749

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] A Type I split cord malformation is a significant pathomechanism of spina bifida aperta in neonates2007

    • Author(s)
      Ogawa A, Tomonoh Y, Hayashi H, Ohta E, R. K, Mori T, Utsunomiya H,Hirose S.
    • Journal Title

      Med. Bull. Fukuoka Univ. 34(4)

      Pages: 261-6

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Midazolam for the treatment of neonatal electroencephalography-confirmed seizures2007

    • Author(s)
      Ogawa A., Shirotani G, Hashimoto J, Hayashi H, Ninomiya S, Ohta, E., Kinoshita R. M, T., Hirose S.
    • Journal Title

      Med. Bull. Fukuoka Univ. 34(4)

      Pages: 267-71

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Focal epilepsy resulting from a de novo SCN1A mutation2007

    • Author(s)
      Okumura A, Kurahashi H, Hirose S, Okawa N, Watanabe K.
    • Journal Title

      Neuropediatrics 38(5)

      Pages: 253-6

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Mutation screening of AP3M2 in Japanese epilepsy patients2007

    • Author(s)
      Hirose S, et. al.
    • Journal Title

      Brain Dev 29(8)

      Pages: 462-467

    • NAID

      10024136602

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Type I split cord malfbmlation is a significant pathomechanism of spina bifida aerta in neonates2007

    • Author(s)
      Hirose S, et. al.
    • Journal Title

      Med.Bull.Fukuoka Univ 34(4)

      Pages: 261-266

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Midazolam for the treatment of neonatal electroencephalography-confirmed seizures2007

    • Author(s)
      Hirose S, et. al.
    • Journal Title

      Med.Bull.Fukuoka Univ 34(4)

      Pages: 267-271

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] High-level and functional exprcssion of a recombinant protein of onion trypsin in hibitor2007

    • Author(s)
      Deshimaru M, et. al.
    • Journal Title

      Fukuoka Univ.Sci.Rep 37

      Pages: 37-44

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Identification of novel serum proteins in a Japanese viper: homologs ofinammalian PSP942007

    • Author(s)
      Deshimam M, et. al.
    • Journal Title

      Biochem.Biophys.Res.Commun (330-334) 27

      Pages: 330-334

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Active fragrpents of the antihemorrhagic protein HSF from serum of habu2007

    • Author(s)
      Deshimaru M, et. al.
    • Journal Title

      Toxicon

      Pages: 653-662

    • Related Report
      2007 Annual Research Report
  • [Journal Article] LGR4 Regulates the Postnatal Development and Integrity of Male Reproductive Tracts in Mice2007

    • Author(s)
      Araki, K., et. al.
    • Journal Title

      Biol.Reprod 76

      Pages: 303-313

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] EMcient conversion of ES cells into myogenic lineage using the gene-inducible system2007

    • Author(s)
      Araki, K, et. al.
    • Journal Title

      Biochcm.Biophys.Res.Commun 357

      Pages: 957-963

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] The interaction of two tethering factors, p115 and COG complex, is required for Golgi integrity.2007

    • Author(s)
      Misumi Y., et al.
    • Journal Title

      Y.Traffic 8(3)

      Pages: 270-284

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Active fragments of the antihemorrhagic protein HSF from serum of habu(Trimeresurus flavoviridis)2007

    • Author(s)
      Deshimaru, M., et al.
    • Journal Title

      Toxicon 49

      Pages: 653-662

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Cell membrane-derived lysophosphatidylcholine activates cardiac ryanodine receptor channels.2007

    • Author(s)
      Uehara A,. et al.
    • Journal Title

      Pflugers Arch. 453(4)

      Pages: 455-462

    • Related Report
      2006 Annual Research Report
  • [Journal Article] LGR4 Regulates the Postnatal Development and Integrity of Male Reproductive Tracts in Mice.2007

    • Author(s)
      Araki K., et al.
    • Journal Title

      Biology of Reproduction 76

      Pages: 303-313

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : prognostic factors and characteristics of plasma amino acid profile2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M.
    • Journal Title

      Pediatr Int 48(2)

      Pages: 105-11

    • NAID

      10018195131

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] A new paradigm of channelopathy in epilepsy syndromes : intracellular trafficking abnormality of channel molecules2006

    • Author(s)
      Hirose S.
    • Journal Title

      Epilepsy Res 70 Suppl 1

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Phenotypes and genotypes in epilepsy with febrile seizures plus2006

    • Author(s)
      Ito M, Yamakawa K, Sugawara T, Hirose S,Fukuma G, Kaneko S.
    • Journal Title

      Epilepsy Res 70 Suppl 1

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype2006

    • Author(s)
      Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    • Journal Title

      Pediatr Neurol 34(3)

      Pages: 235-8

    • Related Report
      2008 Final Research Report
  • [Journal Article] Neuropathology of methylmalonic acidemia in a child2006

    • Author(s)
      Kanaumi T, Takashima S,Hirose S, Kodama T, Iwasaki H.
    • Journal Title

      Pediatr Neurol 34(2)

      Pages: 156-9

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Developmental changes in the expression of GABA_A receptor alpha 1 and gamma 2 subunits in human temporal lobe, hippocampus and basal ganglia : an implication for consideration on age-related epilepsy2006

    • Author(s)
      Kanaumi T, Takashima S, Iwasaki H, Mitsudome A, Hirose S.
    • Journal Title

      Epilepsy Res 71(1) :

      Pages: 47-53

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Ictal midline epileptiform discharges in benign familial neonatal convulsions2006

    • Author(s)
      Ogawa A, Hirose S, Yasumoto S, Ohfu M, Mitsudome A.
    • Journal Title

      Med. Bull. Fukuoka Univ. 33(4)

      Pages: 305-7

    • NAID

      110004830503

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] Involvement of Ca^<(2+)>-induced Ca^<2+> releasing system in interleukin-1β-associated adenosine release2006

    • Author(s)
      Zhu G, Okada M, Yoshida S, Mori F, Hirose S, Wakabayashi K, Kaneko S.
    • Journal Title

      Eur J Pharmacol 532(3)

      Pages: 246-52

    • Related Report
      2008 Final Research Report
    • Peer Reviewed
  • [Journal Article] A new paradigm of channelopathy inepilepsy syndromes : intracellular traffickingabnormality of channel molecules2006

    • Author(s)
      Hirose S
    • Journal Title

      Epilepsy Res 70Suppl 1

    • Related Report
      2008 Self-evaluation Report
  • [Journal Article] Neuropathyology of amethylmalonic Acidemia in a Child2006

    • Author(s)
      Hirose S., et al.
    • Journal Title

      Pediatr Neurol 34

      Pages: 156-159

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Involment of Ca2 + -induced Ca2 + releasing system in interleukin-1β-associated adenosine release2006

    • Author(s)
      Hirose S., et al.
    • Journal Title

      European Journal of Pharmacology 532

      Pages: 246-252

    • Related Report
      2006 Annual Research Report
  • [Journal Article] An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype Running title : An infant of MELAS phenotype2006

    • Author(s)
      Hirose S., et al.
    • Journal Title

      Pediatr Neurol 34(3)

      Pages: 235-238

    • Related Report
      2006 Annual Research Report
  • [Journal Article] A new paradigm of channelopathy in epilepsy syndromes : Intracellular trafficking abnormality of channel molecules2006

    • Author(s)
      Hirose S.
    • Journal Title

      Epilepsy Research 70s

      Pages: 206-217

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Modulation of D-Serine levels via ubiquitin-dependent proteasomal degradation of Serine racemase.2006

    • Author(s)
      Misumi Y., et al.
    • Journal Title

      J.Biol.Chem 281(29):

      Pages: 20291-20302

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Na^+/Ca^<2+>交換体のけいれんに対する役割2006

    • Author(s)
      高野行夫, 斎藤亮他
    • Journal Title

      薬学雑誌 126

      Pages: 138-140

    • Related Report
      2006 Annual Research Report
  • [Journal Article] 侵害的刺激および機械性アロディニアに対するムスカリン受容体作動薬McN-A-343の抗侵害作用2006

    • Author(s)
      高野行夫, 斎藤亮他
    • Journal Title

      薬学雑誌 126

      Pages: 132-134

    • Related Report
      2006 Annual Research Report
  • [Journal Article] ヒトてんかんと同じ遺伝子異常を持つモデル動物2006

    • Author(s)
      高野行夫, 斎藤亮
    • Journal Title

      脳と精神の医学 34(3)

      Pages: 235-238

    • Related Report
      2006 Annual Research Report
  • [Journal Article] ラットを用いた簡便な嘔吐測定法2006

    • Author(s)
      高野行夫, 斎藤亮 他
    • Journal Title

      日本薬理学雑誌 127

      Pages: 461-466

    • NAID

      10018061250

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Impaired expression of Importin/karyopherin 1 leads to post-implantation lethality. Biochem. Biophys.2006

    • Author(s)
      Araki K., et al.
    • Journal Title

      Res.Commun 341

      Pages: 132-138

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Enhanced trypsin activity in pancreatic acinar cells deficient for serine protease inhibitor kazal type 3.2006

    • Author(s)
      Araki K., et al.
    • Journal Title

      Pancreas 33

      Pages: 104-106

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.2006

    • Author(s)
      Araki K., et al.
    • Journal Title

      Hum.Mol.Genet 15

      Pages: 2266-2275

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Negative Selection with the Diphtheria toxin A fragment Gene Improves Frequency of Cre-Mediated Cassette Exchange in ES Cells.2006

    • Author(s)
      Araki K., et al.
    • Journal Title

      J.Biochem 140

      Pages: 793-798

    • NAID

      10018840450

    • Related Report
      2006 Annual Research Report
  • [Journal Article] A novel murine gene, Sickle tail (Skt), linked to the Danforth's short tail (Sd) locus, is required for normal development of the intervertebral disc.2006

    • Author(s)
      Araki K., et al.
    • Journal Title

      Genetics 172

      Pages: 445-456

    • Related Report
      2006 Annual Research Report
  • [Presentation] Mutational analysis for repetitive febrile seizuresand sporadic febrile seizures plus in JapaneseHirose, S2009

    • Author(s)
      Hirose S
    • Organizer
      8th European Congress onEpileptology
    • Place of Presentation
      Berlin
    • Related Report
      2008 Self-evaluation Report
  • [Presentation] Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ22008

    • Author(s)
      Hirose s.
    • Organizer
      8th European Congress on Epileptology
    • Place of Presentation
      . Berlin
    • Year and Date
      2008-09-22
    • Related Report
      2008 Annual Research Report
  • [Presentation] Mutational analysis for repetitive febrile seizures and sporadic febrile seizures plus in Japanese2008

    • Author(s)
      Hirose s.
    • Organizer
      8th European Congress on Epileptology
    • Place of Presentation
      . Berlin
    • Year and Date
      2008-09-20
    • Related Report
      2008 Annual Research Report
  • [Presentation] Recent advances in the genetics of epilepsy Joint2008

    • Author(s)
      Hirose s.
    • Organizer
      7^<th> Human Genome Organization (HUGO)
    • Place of Presentation
      セブ、フィリピン
    • Year and Date
      2008-04-05
    • Related Report
      2008 Annual Research Report
  • [Presentation] Recent advances in the genetics of epilepsyJoint2008

    • Author(s)
      Hirose S.
    • Organizer
      7^<th> Human Genome Organization(HUGO)
    • Place of Presentation
      1-7cebu, Philippine
    • Related Report
      2008 Final Research Report
  • [Presentation] A De Novo KCNQ2 Mutation Detected in Benign Neonatal Convulsions : Possible Involvement Of Genes responsible for Rare Inherited Epilepsy in Idiopathic Epilepsy2008

    • Author(s)
      Ishii A., Fukuma G., Uehara A., Yasukochi M., Miyajima T., Makita Y., Hamachi A., Yonetani M., Inoue T., Okada M., Kaneko S., Hirose S.
    • Organizer
      The 4^<th> Congress of Asian Society for Pediatric Research
    • Place of Presentation
      Hawaii, USA
    • Related Report
      2008 Final Research Report
  • [Presentation] Perinatal Characteristics of Early-Onset Sepsis in Neonatal Intensive Care Unit in Recent Years2008

    • Author(s)
      Tsutsumi M., Ohta E., Inoue T., Kinoshita R., Nakamura M., Mori T., Hirose S.
    • Organizer
      The 4^<th> Congress of Asian Society for Pediatric Research
    • Place of Presentation
      Hawaii, USA
    • Related Report
      2008 Final Research Report
  • [Presentation] The Application of Genetic Tests for Epilepsy-are there Guidelines for Clinicians?2008

    • Author(s)
      Hirose S.
    • Organizer
      7^<th> Asian & Oceanian Epilepsy Congress Xiamen, China
    • Place of Presentation
      Xiamen
    • Related Report
      2008 Final Research Report
  • [Presentation] Genome-Wide Identification of Febrile Seizure and Related Epilepsy Phenotype Loci2008

    • Author(s)
      Miyashita A., Kuwano R., Kojima T., Sasaki T., Zhu G, Kanai K., Fujita K., Hirose S., Kaneko S.
    • Organizer
      7^<th> Asian & Oceanian Epilepsy Congress
    • Place of Presentation
      Xiamen, China
    • Related Report
      2008 Final Research Report
  • [Presentation] EEG Findings on Headache with MELAS2008

    • Author(s)
      Ihara Y., Fujita T., Inoue T., Yasumoto S., Mitsudome A., Hirose S.
    • Place of Presentation
      Xiamen, China
    • Related Report
      2008 Final Research Report
  • [Presentation] Myoclonic-Astatic Epilepsy with Focal Spike Discharge may have Unfavourable Prognosis2008

    • Author(s)
      Ideguchi H., Inoue T., Ninomiya S., Fujita T., Nakamura N., Yasumoto S., Hirose S.
    • Place of Presentation
      Xiamen, China
    • Related Report
      2008 Final Research Report
  • [Presentation] Non-convulsive status Lpilepticuso of Temporal Lobe Epilepsy Misdiagnosed as a Psychosomatic Disease2008

    • Author(s)
      Fujita T., Nakamura N., Inoue T., ninomiya S., Ihara Y., Tomonou Y., Ideguchi H., Yasumoto S., Mitsudome A., Hirose S.
    • Place of Presentation
      Xiamen, China
    • Related Report
      2008 Final Research Report
  • [Presentation] Psychomotor Retardation Aggravated by Infantile Non-convulsive Status Epileptics in Angelman Syndrome2008

    • Author(s)
      Ninomiya S., Nakamura N., Fujita T., Ideguchi H., Inoue T., Yasumoto S., Hirose S.
    • Place of Presentation
      Xiamen, China
    • Related Report
      2008 Final Research Report
  • [Presentation] The present Status and Problem of Plenatal Screening of Congenital Heart Defects ; 4 Major Refernal Centers in Kyusyu, Japan2008

    • Author(s)
      Yoshikane Y., Yoshizato T., Maeno Y., Nishibatake M., Kam N., Fusazaki N., Hirose S.
    • Organizer
      The 2^<nd> Asia-Pacific Congress of Pediatrics Cordiology and Cardiac Surgery
    • Place of Presentation
      Korea
    • Related Report
      2008 Final Research Report
  • [Presentation] Retrospective Analysis of Prenatally Detected Congenital Heart Defects : Six-year Experience of 4 Institutions in Japan2008

    • Author(s)
      Yashikane Y., Yoshizato T., Meno Y., Nishibatake M., Kan N., Fusazaki N.,Hirose S.
    • Organizer
      15^<th> Congress of the FAOPS
    • Place of Presentation
      Nagoya
    • Related Report
      2008 Final Research Report
  • [Presentation] Study of Septicemia Due to Enterbacter Cloacae in a Tertiary Neonatal Intensive Care Unit during 1997-20072008

    • Author(s)
      Ohta E., Setoue T., Tsutsumi M., Inoue S., Kinoshita R., Nakamura M., Mori T., Ogawa A., Hirose S.
    • Organizer
      15^<th> Congress of the FAOPS
    • Place of Presentation
      Nagoya
    • Related Report
      2008 Final Research Report
  • [Presentation] Prognoses of the Neonates of Multiple Births Admitted in NICU in recent Years2008

    • Author(s)
      Inoue T., Tsutsumi M., Kinoshita R., Ohta E., Nakamura M., Mori T., Hirose S.
    • Organizer
      15th Congress of the FAOPS
    • Place of Presentation
      Nagoya
    • Related Report
      2008 Final Research Report
  • [Presentation] Mutational analysis for repetitive febrile seizures and sporadic febrile seizures plus in Japanese2008

    • Author(s)
      Hirose, S.
    • Organizer
      8th European Congress on Epileptology
    • Place of Presentation
      Berlin
    • Related Report
      2008 Final Research Report
  • [Presentation] Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2 8th European Congress on Epileptology2008

    • Place of Presentation
      Berlin
    • Related Report
      2008 Final Research Report
  • [Presentation] Update on the genetics of Epilepsy : Potential clinical applications2008

    • Author(s)
      Hirose S
    • Organizer
      Annual meeting for Thai Child Neurology Society
    • Place of Presentation
      Thailand
    • Related Report
      2008 Self-evaluation Report
  • [Presentation] Benign childhood epilepsy with centrotemporalspikes following benign neonatal seizures resultingfrom a mutation of KCNQ2 Hirose, S2008

    • Author(s)
      Hirose S
    • Organizer
      8^<th> European Congress on Epileptology European Congress on Epileptology
    • Place of Presentation
      Berlin
    • Related Report
      2008 Self-evaluation Report
  • [Presentation] The Application of Genetic Tests for Epilepsy-arethere Guidelines for Clinicians?2008

    • Author(s)
      Hirose S
    • Organizer
      7^<th> Asian &amp; Oceanian Epilepsy Congress Xiamen,China
    • Place of Presentation
      Xiamen
    • Related Report
      2008 Self-evaluation Report
  • [Presentation] Recent advances in the genetics of epilepsyJoint/Hirose S2008

    • Author(s)
      Hirose S
    • Organizer
      7^<th> Human Genome Organization(HUGO)
    • Place of Presentation
      セブ,フィリピン
    • Related Report
      2008 Self-evaluation Report
  • [Presentation] A Girl with bronchiolitis obiterans presenting recurrent lobar atelectasis2007

    • Author(s)
      Fujiwara C., Yoshikane Y., Tanaks M., Hiratsuka M., Iwasaki N., Shirakusa T., Yamaguchi S., Hiriose S.
    • Organizer
      25^<th> International Congress of Pediatrics
    • Place of Presentation
      Athenes, Greece
    • Related Report
      2008 Final Research Report
  • [Presentation] Pediarictors of surgical treatment for patient ductus arteriosus in extremely low birth weight infants2007

    • Author(s)
      Yoshikane Y., Mori T., Yukitake K., Hirose S.
    • Organizer
      25^<th> International Congres of Pediatrics
    • Place of Presentation
      Athenes, Greece
    • Related Report
      2008 Final Research Report
  • [Presentation] Fetal infection of Hilicobacter cinaedi manifested by fetal distress and mucous diarrhea at birth2007

    • Author(s)
      Ohta E., Fujiwara C., Mori T., Ogawa A., Adachi M., Obama H., Kawarabayashi T., Yamaguchi S.,Ono J., Hirose S.
    • Organizer
      25^<th> International Congress of Pediatrics
    • Place of Presentation
      Athenes, Greece
    • Related Report
      2008 Final Research Report
  • [Presentation] Micro deletional Mutation of SCN1A in Individuals with Severe Myoclonic Epilepsy in Fancy(SMEI) and Borderline SMEI2007

    • Author(s)
      Wang J., Kurahashi K., Hamachi A., Yonetani M., Inoue T., Ogawa A., Hirose S., Yasumoto S., Kaneko S.
    • Organizer
      27^<th> International Epilepsy Congress
    • Place of Presentation
      Singapole
    • Related Report
      2008 Final Research Report
  • [Presentation] Midazolam for the treatment of neonatal EEG-confirmed seizures2007

    • Author(s)
      Ogawa A., Shiratani G, Hashimoto J., Mori S., Yukitake K., Hirose S.
    • Organizer
      27^<th> International Epilepsy Congress
    • Place of Presentation
      Singapore
    • Related Report
      2008 Final Research Report
  • [Presentation] Mutation screening of AP3M2 in Japanese epilepsy/Ming2007

    • Author(s)
      Hirose S., et. al.
    • Organizer
      HUGO's 12th Human Genome Mceting
    • Place of Presentation
      Montreal
    • Related Report
      2007 Annual Research Report
  • [Presentation] MICRO DELETION OF SCNIA IS ASSOCIAITED NOT ONLY、 WITH SEVERE MYOCL ONIC EPILEPSY INFANCY BUT ALSO、 WITH ITS BODERLINE PHENOTYPE2007

    • Author(s)
      Hirose S., et. al.
    • Organizer
      the International congress of Pediatrics
    • Place of Presentation
      Athens Greece
    • Related Report
      2007 Annual Research Report
  • [Patent(Industrial Property Rights)] てんかんモデル非ヒト哺乳動物2009

    • Inventor(s)
      廣瀬伸一
    • Industrial Property Rights Holder
      (独)科学技術振興機構
    • Filing Date
      2009-02-10
    • Related Report
      2008 Final Research Report
  • [Patent(Industrial Property Rights)] 変異導入遺伝子およびそれを導入したノックイン非ヒト動物2008

    • Inventor(s)
      廣瀬伸一
    • Industrial Property Rights Holder
      (独)科学技術振興機構
    • Industrial Property Number
      2008-273446
    • Filing Date
      2008-10-23
    • Related Report
      2008 Final Research Report
  • [Patent(Industrial Property Rights)] てんかんモデル非ヒト哺乳動物2008

    • Inventor(s)
      廣瀬伸一
    • Industrial Property Rights Holder
      (独)科学技術振興機構
    • Industrial Property Number
      2008-031002
    • Filing Date
      2008-02-12
    • Related Report
      2008 Final Research Report
  • [Patent(Industrial Property Rights)] 変異導入遺伝子およびそれを導入したノックイン非ヒト動物2008

    • Inventor(s)
      廣瀬伸一, 弟子丸正伸, 荒木喜美
    • Industrial Property Rights Holder
      廣瀬伸一
    • Industrial Property Number
      2008-273446
    • Filing Date
      2008-10-23
    • Related Report
      2008 Annual Research Report 2008 Self-evaluation Report

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Published: 2006-04-01   Modified: 2016-04-21  

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