Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency
Ichiyama, Masako, Ohga, Shouichi, Ochiai, Masayuki, Fukushima, Kotaro, Ishimura, Masataka, Torio, Michiko, Urata, Michiyo, Hotta, Taeko, Kang, Dongchon, Hara, Toshiro
Published in Brain & development (Tokyo. 1979) (01.02.2016)
Published in Brain & development (Tokyo. 1979) (01.02.2016)
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Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection
Okuzono, Sayaka, Ishimura, Masataka, Kanno, Shunsuke, Sonoda, Motoshi, Kaku, Noriyuki, Motomura, Yoshitomo, Nishio, Hisanori, Oba, Utako, Hanada, Masuo, Fukushi, Jun-Ichi, Urata, Michiyo, Kang, Dongchon, Takada, Hidetoshi, Ohga, Shouichi
Published in Annals of clinical microbiology and antimicrobials (09.07.2018)
Published in Annals of clinical microbiology and antimicrobials (09.07.2018)
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Toxic myopathy with multiple deletions in mitochondrial DNA associated with long‐term use of oral anti‐viral drugs for hepatitis B: A case study
Fujii, Takayuki, Takase, Kei‐ichiro, Honda, Hiroyuki, Kawamura, Nobutoshi, Yamasaki, Ryo, Urata, Michiyo, Uchiumi, Takeshi, Iwaki, Toru, Kira, Jun‐ichi
Published in Neuropathology (01.04.2019)
Published in Neuropathology (01.04.2019)
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A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period
Unal, Sule, Gumruk, Fatma, Yigit, Sule, Tuncer, Murat, Tavil, Betul, Cil, Onur, Takci, Sahin, Urata, Michiyo, Hotta, Taeko, Kang, Dongchon, Cetin, Mualla
Published in Pediatric blood & cancer (01.04.2014)
Published in Pediatric blood & cancer (01.04.2014)
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Journal Article
High-Sensitivity Detection of the A3243G Mutation of Mitochondrial DNA by a Combination of Allele-Specific PCR and Peptide Nucleic Acid-Directed PCR Clamping
Urata, Michiyo, Wada, Yui, Kim, Sang Ho, Chumpia, Worawan, Kayamori, Yuzo, Hamasaki, Naotaka, Kang, Dongchon
Published in Clinical chemistry (Baltimore, Md.) (01.11.2004)
Published in Clinical chemistry (Baltimore, Md.) (01.11.2004)
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Journal Article
Factor XII gene (F12) -4C/C polymorphism in combination with low protein S activity is associated with deep vein thrombosis
Kanaji, Taisuke, Watanabe, Kumiko, Hattori, Sachiko, Urata, Michiyo, Iida, Hiroko, Kinoshita, Sachiko, Kayamori, Yuzo, Kang, Dongchon, Hamasaki, Naotaka
Published in Thrombosis and haemostasis (01.12.2006)
Published in Thrombosis and haemostasis (01.12.2006)
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Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan
Ikematsu, Hideyuki, Chong, Yong, Shirane, Kenjiro, Toh, Hidehiro, Sasaki, Hiroyuki, Koga, Yui, Urata, Michiyo, Hotta, Taeko, Uchiumi, Takeshi, Kang, Donchon
Published in Fukuoka igaku zasshi = Hukuoka acta medica (01.01.2015)
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Published in Fukuoka igaku zasshi = Hukuoka acta medica (01.01.2015)
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A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene
Iida, H, Ishii, E, Nakahara, M, Urata, M, Wakiyama, M, Kurihara, M, Watanabe, K, Kai, T, Ihara, K, Kinoshita, S, Hamasaki, N
Published in Thrombosis and haemostasis (01.07.2000)
Published in Thrombosis and haemostasis (01.07.2000)
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Journal Article
The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene
Inoue, Hirofumi, Terachi, Shin‐ichi, Uchiumi, Takeshi, Sato, Tetsuji, Urata, Michiyo, Ishimura, Masataka, Koga, Yui, Hotta, Taeko, Hara, Toshiro, Kang, Dongchon, Ohga, Shouichi
Published in Pediatric blood & cancer (01.07.2017)
Published in Pediatric blood & cancer (01.07.2017)
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Journal Article
The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene: Inoue et al
Inoue, Hirofumi, Terachi, Shin-ichi, Uchiumi, Takeshi, Sato, Tetsuji, Urata, Michiyo, Ishimura, Masataka, Koga, Yui, Hotta, Taeko, Hara, Toshiro, Kang, Dongchon, Ohga, Shouichi
Published in Pediatric blood & cancer (01.07.2017)
Published in Pediatric blood & cancer (01.07.2017)
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Journal Article
A basic study of determination matrix metalloproteinase-3 and carbohydrate in rheumatoid factor in serum for diagnosis of rheumatoid arthritis
Urata, Michiyo, Nakamura, Nobuko, Kinoshita, Sachiko, Kayamori, Yuzo, Hamasaki, Naotaka
Published in Rinsho byori. The Japanese journal of clinical pathology (01.08.2003)
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Published in Rinsho byori. The Japanese journal of clinical pathology (01.08.2003)
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Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy
Ishimura, Masataka, Saito, Mitsumasa, Ohga, Shouichi, Hoshina, Takayuki, Baba, Haruhisa, Urata, Michiyo, Kira, Ryutaro, Takada, Hidetoshi, Kusuhara, Koichi, Kang, Dongchon, Hara, Toshiro
Published in European journal of pediatrics (01.06.2009)
Published in European journal of pediatrics (01.06.2009)
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Journal Article
Protein S deficiency in three patients with thrombosis
Minami, R, Urata, M, Kurihara, M, Hara, K, Abe, Y, Muta, K, Nawata, H
Published in Rinshō ketsueki (01.08.2001)
Published in Rinshō ketsueki (01.08.2001)
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Journal Article
Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: Effects on secretion and anticoagulant activity of protein S
Tsuda, Hiroko, Urata, Michiyo, Tsuda, Tomohide, Wakiyama, Machiko, Iida, Hiroko, Nakahara, Mutsuko, Kinoshita, Sachiko, Hamasaki, Naotaka
Published in Thrombosis research (01.02.2002)
Published in Thrombosis research (01.02.2002)
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Journal Article
Successful therapy with argatroban for superior mesenteric vein thrombosis in a patient with congenital antithrombin deficiency
Muta, Tsuyoshi, Okamura, Takashi, Kawamoto, Masahiko, Ichimiya, Hitoshi, Yamanaka, Motoko, Wada, Yui, Urata, Michiyo, Kayamori, Yuzo, Hamasaki, Naotaka, Kato, Koji, Eto, Testuya, Gondo, Hisashi, Shibuya, Tsunefumi
Published in European journal of haematology (01.08.2005)
Published in European journal of haematology (01.08.2005)
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Journal Article
Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency
Tsuda, Hiroko, Urata, Michiyo, Tsuda, Tomohide, Wakiyama, Machiko, Iida, Hiroko, Nakahara, Mutsuko, Kinoshita, Sachiko, Hamasaki, Naotaka
Published in Thrombosis research (01.02.2002)
Published in Thrombosis research (01.02.2002)
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Journal Article
New sensitive method for the detection of the A3243G mutation of human mitochondrial deoxyribonucleic acid in diabetes mellitus patients by ligation-mediated polymerase chain reaction
Urata, Michiyo, Wakiyama, Machiko, Iwase, Masanori, Yoneda, Makoto, Kinoshita, Sachiko, Hamasaki, Naotaka, Kang, Dongchon
Published in Clinical chemistry (Baltimore, Md.) (01.10.1998)
Published in Clinical chemistry (Baltimore, Md.) (01.10.1998)
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Journal Article
Failure in the Detection of Aberrant mRNA from the Heterozygotic Splice Site Mutant Allele for Protein S in a Patient with Protein S Deficiency
Iida, Hiroko, Nakahara, Mutsuko, Komori, Kimihiro, Fujise, Masako, Wakiyama, Machiko, Urata, Michiyo, Kinoshita, Sachiko, Tsuda, Hiroko, Sugimachi, Keizo, Hamasaki, Naotaka
Published in Thrombosis research (01.05.2001)
Published in Thrombosis research (01.05.2001)
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