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Shigeru Tsuchiya

Showing results (61-70 of 110) with videos related to

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Epilepsy Research|April 21, 2009
Reduced levels of interleukin-1 receptor antagonist in the cerebrospinal fluid in patients with West syndromeKazuhiro Haginoya, Rie Noguchi, Yajuan Zhao, et al.
Journal of Child Neurology|March 7, 2009
Smith-Magenis syndrome with West syndrome in a 5-year-old girl: a long-term follow-up studyNaomi Hino-Fukuyo, Kazuhiro Haginoya, Mitsugu Uematsu, et al.
The Journal of Molecular Diagnostics : JMD|February 1, 2005
Consensus JH gene probes with conjugated 3'-minor groove binder for monitoring minimal residual disease in acute lymphoblastic leukemiaMichihiro Uchiyama, Chihaya Maesawa, Akiko Yashima-Abo, et al.
Human Genetics|February 20, 2003
Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese familiesNorimoto Kobayashi, Kazunaga Agematsu, Kanji Sugita, et al.
Journal of Pediatric Hematology/Oncology|November 23, 2006
The first infant case with hepatosplenic gammadelta T-cell lymphoma after acute disseminated encephalomyelitis (ADEM)-like exacerbationShinichiro Y Koga, Satoru Kumaki, Ryo Ichinohasama, et al.
Journal of Child Neurology|February 3, 2009
Ictal vomiting as an initial symptom of severe myoclonic epilepsy in infancy: a case reportNaomi Hino-Fukuyo, Kazuhiro Haginoya, Noriko Togashi, et al.
The Journal of Experimental Medicine|February 9, 2011
Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cellsMasako Saito, Masayuki Nagasawa, Hidetoshi Takada, et al.
Endocrinology|December 16, 2006
All-trans retinoic acid induces in vitro angiogenesis via retinoic acid receptor: possible involvement of paracrine effects of endogenous vascular endothelial growth factor signalingAkiko Saito, Akira Sugawara, Akira Uruno, et al.
Human Mutation|May 28, 2010
Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndromeTojo Nakayama, Ikuo Ogiwara, Koichi Ito, et al.
British Journal of Haematology|July 9, 2002
Treatment responses of childhood aplastic anaemia with chromosomal aberrations at diagnosisShouichi Ohga, Akira Ohara, Shigeyoshi Hibi, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Epilepsy Research|April 21, 2009
Reduced levels of interleukin-1 receptor antagonist in the cerebrospinal fluid in patients with West syndromeKazuhiro Haginoya, Rie Noguchi, Yajuan Zhao, et al.
Journal of Child Neurology|March 7, 2009
Smith-Magenis syndrome with West syndrome in a 5-year-old girl: a long-term follow-up studyNaomi Hino-Fukuyo, Kazuhiro Haginoya, Mitsugu Uematsu, et al.
The Journal of Molecular Diagnostics : JMD|February 1, 2005
Consensus JH gene probes with conjugated 3'-minor groove binder for monitoring minimal residual disease in acute lymphoblastic leukemiaMichihiro Uchiyama, Chihaya Maesawa, Akiko Yashima-Abo, et al.
Human Genetics|February 20, 2003
Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese familiesNorimoto Kobayashi, Kazunaga Agematsu, Kanji Sugita, et al.
Journal of Pediatric Hematology/Oncology|November 23, 2006
The first infant case with hepatosplenic gammadelta T-cell lymphoma after acute disseminated encephalomyelitis (ADEM)-like exacerbationShinichiro Y Koga, Satoru Kumaki, Ryo Ichinohasama, et al.
Journal of Child Neurology|February 3, 2009
Ictal vomiting as an initial symptom of severe myoclonic epilepsy in infancy: a case reportNaomi Hino-Fukuyo, Kazuhiro Haginoya, Noriko Togashi, et al.
The Journal of Experimental Medicine|February 9, 2011
Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cellsMasako Saito, Masayuki Nagasawa, Hidetoshi Takada, et al.
Endocrinology|December 16, 2006
All-trans retinoic acid induces in vitro angiogenesis via retinoic acid receptor: possible involvement of paracrine effects of endogenous vascular endothelial growth factor signalingAkiko Saito, Akira Sugawara, Akira Uruno, et al.
Human Mutation|May 28, 2010
Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndromeTojo Nakayama, Ikuo Ogiwara, Koichi Ito, et al.
British Journal of Haematology|July 9, 2002
Treatment responses of childhood aplastic anaemia with chromosomal aberrations at diagnosisShouichi Ohga, Akira Ohara, Shigeyoshi Hibi, et al.
Pageof 11