 石川暢恒SHIKAWA,Nobutsune |
・Nobutsune Ishikawa, Yoshiyuki Kobayashi, Masao Kobayashi. A case of frontal lobe epilepsy in which amplitude-integrated EEG combined with conventional EEG was useful for evaluating clusters of seizures. Epilepsy & Behaviour; 18: 485-487, 2010 |
| ・Nobutsune Ishikawa , Masao Kobayashi. Recurrent acute cerebellar ataxia associated with anti-cardiolipin antibodies. Brain & Development; 32: 588-591, 2010 | |
| ・石川暢恒、小林正夫．HAX1遺伝子変異を有する重症先天性好中球減少症に合併する中枢神経症状の検討．脳と発達; 41: 415-419, 2009 | |
| ・Nobutsune Ishikawa, Go Tajima, Hiroaki Ono, Masao Kobayashi. Different neuroradiological findings during two stroke-like episodes in a patient with a congenital disorder of glycosylation type Ia. Brain & Development; 31: 240-243, 2009 | |
| ・Nobutsune Ishikawa, Go Tajima, Masao Kobayashi. Epileptic spasms after stem cell transplantation for chronic Epstein-Barr virus infection. Pediatric Neurology; 40: 404-407, 2009 | |
| ・石川暢恒、川口浩史、宮河真一郎、佐藤貴、西村真一郎、小林正夫．Posterior reversible encephalopathy syndromeと考えられた７例の検討．小児科学会雑誌; 113: 64-68, 2009 | |
| ・石川暢恒、但馬剛、小林正夫．失語症状の改善後ミオクロニー発作を呈するLandau-Kleffner症候群の１例．臨床脳波; 51: 316-319, 2009 | |
| ・Nobutsune Ishikawa, Satoshi Okada, Mizuka Miki, Kenichiro Shirao, Hirotaka Kihara, Miyuki Tsumura, Kazuhiro Nakamura, Hiroshi Kawaguchi, Motoaki Ohtsubo, Shinユichiro Yasunaga, Kousaku Matsubara, Masahiro Sako, Junichi Hara, Masaaki Shiohara, Seiji Kojima, Takashi Sato, Yoshihiro Takihara, Masao Kobayashi. Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene. Journal of Medical Genetics; 45: 802-807, 2008 | |
| ・Yoko Hiraki, Miyuki Moriuchi, Nobuhiko Okamoto, Nobutsune Ishikawa, yosuke Sugimoto, Kuniki Eguchi, Haruya Sakai, Hirotomo Saitsu, Takeshi Mizuguchi, Naoki Harada, Naomichi Matsumoto. Craniosynostosis in a patient with a de novo 15q15-q22 deletion. Amrican Journal of Medical Genetics part A; 146A: 1462-1465, 2008 | |
| ・Ohtsubo M, Yasunaga S, Ohno Y, Tsumura M, Okada S, Ishikawa N, Shirao K, Kikuchi A, Nishitani H, Kobayashi M, Takihara Y. Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity. Proc Natl Acad Sci U S A; 105: 10396-10401, 2008 | |
| ・Nobutsune Ishikawa, Go Tajima, Sumio Hyodo, Yukitoshi Takahashi, Masao Kobayashi. Detection of autoantibodies against NMDA-type glutamate receptor in a patient with recurrent optic neuritis and transient cerebral lesions. Neuropediatrics; 38: 257-260, 2007 | |
| ・Nobutsune Ishikawa, Satoshi Okada, Takashi Sato, Shin'ichiro Yasunaga, Motoaki Ohtsubo, Yoshihiro Takihara, Masao Kobayashi. A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients. Blood Coagulation and Fibrinolysis; 18:519-523, 2007 | |
| ・Satoshi Okada, Nobutsune Ishikawa, Kenichiro Shirao, Hiroshi Kawaguchi, Miyuki Tsumura, Yoshinori Ohno, Shin'ichiro Yasunaga, Motoaki Ohtsubo, Yoshihiro Takihara, Masao Kobayashi. The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-gamma receptor 1 and has a dominant-negative effect on interferon-gamma signal transduction. Journal of Medical Genetics; 44: 485-491, 2007 | |
| ・Nobutsune Ishikawa, Go Tajima, Noriko Yofune, Shinichiro Nishimura, Masao Kobayashi. Moyamoya syndrome after cranial irradiation for bone marrow transplantation in a patient with acute leukemia. Neuropediatrics; 37:1-3, 2006 | |
| ・Yasuhiko Sera, Hiroshi Kawaguchi, Kazuhiro Nakamura, Takashi Sato, Masakazu Habara, Satoshi Okada, Nobutsune Ishikawa, Seji Kojima, Osamu Katoh, Masao Kobayashi. A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia. Haematologica; 90: 1032-1041, 2005 | |
| ・石川暢恒 木原裕貴、大西博之．HBV DNA定量が有用であった母子感染によるB型急性肝炎の１乳児例．小児科臨床；57：459-462，2004 | |
| ・石川暢恒、木原裕貴、大西博之．幼児期に痙攣重積で発症した家族性脳内海綿状血管種の１例．小児科；44：１556-1572，2003 |