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Keiko Nomura

Research Profile

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Japan

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X Chromosome

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TOP 3
Keiko Nomura; Asahito Hama; Akihiro Hoshino; Seiji Kojima; Toshio Miyawaki; Hirokazu Kanegane
Neutropenia and myeloid dysplasia in a patient with delayed-onset adenosine deaminase deficiency.
Keisuke Otsubo; Toshio Miyawaki; Keiko Nomura; Hirokazu Kanegane
Nocturnal enuresis as a first manifestation of acute lymphoblastic leukemia.
Hirokazu Kanegane; Tadashi Ariga; Michael S Hershfield; Kohsuke Imai; Keiko Nomura; Ines Santisteban; Hiromichi Taneichi; Taizo Wada; Akihiro Yachie; Toshio Miyawaki
Successful bone marrow transplantation with reduced intensity conditioning in a patient with delayed-onset adenosine deaminase deficiency.

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All Publications

2013: Keiko Nomura; Asahito Hama; Akihiro Hoshino; Seiji Kojima; Toshio Miyawaki; Hirokazu Kanegane
Neutropenia and myeloid dysplasia in a patient with delayed-onset adenosine deaminase deficiency.
Pediatric blood & cancer 2013;60(5):885-6.
2013: Keisuke Otsubo; Toshio Miyawaki; Keiko Nomura; Hirokazu Kanegane
Nocturnal enuresis as a first manifestation of acute lymphoblastic leukemia.
Pediatrics international : official journal of the Japan Pediatric Society 2013;55(1):126-7.
2013: Hirokazu Kanegane; Tadashi Ariga; Michael S Hershfield; Kohsuke Imai; Keiko Nomura; Ines Santisteban; Hiromichi Taneichi; Taizo Wada; Akihiro Yachie; Toshio Miyawaki
Successful bone marrow transplantation with reduced intensity conditioning in a patient with delayed-onset adenosine deaminase deficiency.
Pediatric transplantation 2013;17(1):E29-32.
2012: Keisuke Otsubo; Akihiro Abe; Sadashi Horie; Toshio Miyawaki; Keiko Nomura; Hirokazu Kanegane
Acute promyelocytic leukemia following aleukemic leukemia cutis harboring NPM/RARA fusion gene.
Pediatric blood & cancer 2012;59(5):959-60.
2012: Hideyuki Nakaoka; Keiko Nomura; Shigeaki Nonoyama; Osamu Ohara; Shunichiro Takezaki; Hiromichi Taneichi; Taizo Wada; Akihiro Yachie; Masafumi Yamada; Xi Yang; Tadashi Ariga; Michael S Hershfield; Kohsuke Imai; Chikako Kamae; Hirokazu Kanegane; Kazushi Miya; Toshio Miyawaki
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis.
International journal of hematology 2012;95(6):692-6.
2011: Keiko Nomura; Keisuke Otsubo; Hiroshi Wakiguchi; Hirokazu Kanegane; Yoshihito Kasahara; Yukihiro Noda; Toshio Miyawaki
Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection.
International journal of hematology 2011;93(6):760-4.
2010: Keisuke Otsubo; Hirokazu Kanegane; Mariko Eguchi; Minenori Eguchi-Ishimae; Kentaro Tamura; Keiko Nomura; Akihiro Abe; Eiichi Ishii; Toshio Miyawaki
ETV6-ARNT fusion in a patient with childhood T lymphoblastic leukemia.
Cancer genetics and cytogenetics 2010;202(1):22-6.
2009: Hirokazu Kanegane; Keiko Nomura; Akihiro Abe; Teruhiko Makino; Shin Ishizawa; Tadamichi Shimizu; Tomoki Naoe; Toshio Miyawaki
Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastocytosis.
International journal of hematology 2009;89(1):86-90.
2008: Keisuke Otsubo; Hirokazu Kanegane; Keiko Nomura; Toshio Miyawaki; Shin Ishizawa
Atypical lymphoproliferative disorder in a patient with X-linked thrombocytopenia.
Pediatric blood & cancer 2008;51(3):443-4.
2008: Jiro Ogawa; Hirokazu Kanegane; Koichi tsuneyama; Rika Kanezaki; Takeshi Futatani; Keiko Nomura; Shin Ishizawa; Masakiyo Sasahara; Etsuro Ito; Toshio Miyawaki
Platelet-derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder.
European journal of haematology 2008;81(1):58-64.
2008: Hideo Hamada; Masanori Kurimoto; Nakamasa Hayashi; Shoichi Nagai; Kunikazu Kurosaki; Kazuhiro Nomoto; Hirokazu Kanegane; Keiko Nomura; Shunro Endo
Pilomyxoid astrocytoma in a patient presenting with fatal hemorrhage. Case report.
Journal of neurosurgery. Pediatrics 2008;1(3):244-6.
2007: Hirokazu Kanegane; Sayaka Watanabe; Keiko Nomura; Gang Xu; Etsuro Ito; Toshio Miyawaki
Distinct clones are associated with the development of transient myeloproliferative disorder and acute megakaryocytic leukemia in a patient with Down syndrome.
International journal of hematology 2007;86(3):250-2.
2006: Naoki Yoshimura; Hirohisa Murakami; Shingo Otaka; Kazuhiro Watanabe; Sayaka Watanabe; Keiichiro Uese; Keiko Nomura; Ikuo Hashimoto; Hirokazu Kanegane; Fukiko Ichida; Takuro Misaki
Open heart operation in a child with congenital heart disease and hereditary spherocytosis.
Circulation journal : official journal of the Japanese Circulation Society 2006;70(12):1655-7.
2006: Hiromichi Taneichi; Hirokazu Kanegane; Takeshi Futatani; Keisuke Otsubo; Keiko Nomura; Yuya Sato; Asahito Hama; Seiji Kojima; Urara Kohdera; Takahide Nakano; Hiroki Hori; Hisashi Kawashima; Yoko Inoh; Junji Kamizono; Naoto Adachi; Yuko Osugi; Haruo Mizuno; Noriko Hotta; Hiroshi Yoneyama; Eiji Nakashima; Shiro Ikegawa; Toshio Miyawaki
Clinical and genetic analyses of presumed Shwachman-Diamond syndrome in Japan.
International journal of hematology 2006;84(1):60-2.
2005: Taketoshi Yoshida; Hirokazu Kanegane; Keisuke Otsubo; Keiko Nomura; Shinichiro Hirokawa; Koichi tsuneyama; Hiroto Egawa; Toshio Miyawaki
Acute lymphoblastic leukemia after living donor liver transplantation.
Pediatrics international : official journal of the Japan Pediatric Society 2005;47(5):579-82.
2005: Hirokazu Kanegane; Hiromichi Taneichi; Keiko Nomura; Takeshi Futatani; Toshio Miyawaki
Severe neutropenia in Japanese patients with x-linked agammaglobulinemia.
Journal of clinical immunology 2005;25(5):491-5.
2005: Hirokazu Kanegane; Yoshihito Kasahara; Jun Okamura; Teruaki Hongo; Rieko Tanaka; Keiko Nomura; Seiji Kojima; Toshio Miyawaki
Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
British journal of haematology 2005;129(3):432-4.
2005: Hirokazu Kanegane; Yoshikiyo Ito; Koichi Ohshima; Takeshi Shichijo; Kunio Tomimasu; Keiko Nomura; Takeshi Futatani; Ryo Sumazaki; Toshio Miyawaki
X-linked lymphoproliferative syndrome presenting with systemic lymphocytic vasculitis.
American journal of hematology 2005;78(2):130-3.
2004: Masahito Tsurusawa; Motoaki Chin; Asayuki Iwai; Keiko Nomura; Hideaki Maeba; Takashi Taga; Tatsuo Higa; Tomoko Kuno; Toshinori Hori; Akiko Muto; Miyo Yamagata
L-Asparagine depletion levels and L-asparaginase activity in plasma of children with acute lymphoblastic leukemia under asparaginase treatment.
Cancer chemotherapy and pharmacology 2004;53(3):204-8.
2002: Hirokazu Kanegane; Keiko Nomura; Toshio Miyawaki; Giovanna Tosato
Biological aspects of Epstein-Barr virus (EBV)-infected lymphocytes in chronic active EBV infection and associated malignancies.
Critical reviews in oncology/hematology 2002;44(3):239-49.
2002: Hirokazu Kanegane; Keiko Nomura; Takeshi Futatani; Toshio Miyawaki
[Intravenous immunoglobulin replacement therapy in X-linked agammaglobulinemia].
Nihon Rinshō Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2002;25(4):337-43.
2001: Hirokazu Kanegane; Takeshi Futatani; Yue Wang; Keiko Nomura; K Shinozaki; Hiroyoshi Matsukura; T Kubota; Satoshi Tsukada; Toshio Miyawaki
Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis.
The Journal of allergy and clinical immunology 2001;108(6):1012-20.
2001: Hideyuki Uotani; Shinichiro Hirokawa; F Saito; Katsunori Tauchi; M Shimoda; Shin Ishizawa; Makoto Kawaguchi; Keiko Nomura; Hirokazu Kanegane; Kazuhiro Tsukada
Non-Hodgkin's lymphoma of the ascending colon in a patient with becker muscular dystrophy: report of a case.
Surgery today 2001;31(11):1016-9.
2000: Keiko Nomura; Hirokazu Kanegane; H Karasuyama; Satoshi Tsukada; Kazunaga Agematsu; G Murakami; S Sakazume; M Sako; R Tanaka; Y Kuniya; T Komeno; S Ishihara; K Hayashi; Tadamitsu Kishimoto; Toshio Miyawaki
Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway.
Blood 2000;96(2):610-7.
2000: Hirokazu Kanegane; Satoshi Tsukada; T Iwata; Takeshi Futatani; Keiko Nomura; J Yamamoto; T Yoshida; Kazunaga Agematsu; Atsushi Komiyama; Toshio Miyawaki
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.
Clinical and experimental immunology 2000;120(3):512-7.