Search Results - "Fukuda, Kazuyoshi"

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  1. 1

    Involvement of the ADAMTS13-VWF axis in acute Kawasaki disease and effects of intravenous immunoglobulin by Tsujii, Nobuyuki, Nogami, Keiji, Matsumoto, Masanori, Yoshizawa, Hiroyuki, Takase, Toshio, Tanaka, Ichiro, Sakai, Toshiyuki, Fukuda, Kazuyoshi, Hayakawa, Masaki, Sakai, Kazuya, Isonishi, Ayami, Matsuura, Kayoko, Fujimura, Yoshihiro, Shima, Midori

    Published in Thrombosis research (01-07-2019)
    “…ADAMTS13 modulates shear-dependent platelet thrombus formation (PTF) by limited proteolysis of von Willebrand factor (VWF). A high-plasma-ratio of VWF antigen…”
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    Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation by TAMAMORI, Akiko, OKANO, Yoshiyuki, OZAKI, Hajime, FUJIMOTO, Akie, KAJIWARA, Masue, FUKUDA, Kazuyoshi, KOBAYASHI, Keiko, SAHEKI, Takeyori, TAGAMI, Yasuko, YAMANO, Tsunekazu

    Published in European journal of pediatrics (01-11-2002)
    “…Adult-onset type 2 citrullinaemia (CTLN2) is caused by a deficiency of the citrin protein encoded by the SLC25A13 gene. Citrin, an aspartate glutamate carrier…”
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    Journal Article
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    A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis by Sakakibara, Takafumi, Takahashi, Yukihiro, Fukuda, Kazuyoshi, Inoue, Tomomi, Kurosawa, Tomoko, Nishikubo, Toshiya, Shima, Midori, Taoka, Toshiaki, Aida, Noriko, Tsujino, Seiichi, Kanazawa, Naomi, Yoshioka, Akira

    Published in Brain & development (Tokyo. 1979) (01-09-2007)
    “…We encountered a male infant with infantile Alexander disease presenting with megalencephaly and hydrocephalus as a neonate and subtle seizures at 3 months of…”
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    Postoperative vesico ureteral reflux recurrence diagnosed by positioning the instillation of contrast cystography : a case report by Fukui, Shinji, Aoki, Katsuya, Nakai, Yasushi, Matsumoto, Yoshihiro, Kagebayashi, Yoriaki, Fukuda, Kazuyoshi, Samma, Shoji

    Published in Hinyokika kiyo. Acta urologica Japonica (01-11-2013)
    “…A 5-year-old boy was diagnosed with febrile urinary tract infection (UTI) at the age of 2 months. Voiding cystourethrography (VCUG) showed grade IV reflux on…”
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    Inversions of the factor VIII gene in Japanese patients with severe hemophilia A by FUKUDA, Kazuyoshi, NAKA, Hiroyuki, MORICHIKA, Shogo, SHIBATA, Masaru, TANAKA, Ichiro, SHIMA, Midori, YOSHIOKA, Akira

    Published in International journal of hematology (01-04-2004)
    “…Hemophilia A is genetically very heterogeneous because disease-causing mutations involving deletions, point mutations, insertions, and inversions are scattered…”
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  8. 8

    Assessment of Platelet Thrombus Formation under Flow Conditions in Patients with Acute Kawasaki Disease by Tsujii, Nobuyuki, Nogami, Keiji, Yoshizawa, Hiroyuki, Sakai, Toshiyuki, Fukuda, Kazuyoshi, Ishiguro, Akira, Shima, Midori

    Published in The Journal of pediatrics (01-11-2020)
    “…To assess platelet thrombus formation (PTF) under flow conditions in patients with Kawasaki disease. Previously available platelet activation data were limited…”
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    ROTEM could be useful for lupus anticoagulant hypoprothrombinemia syndrome by Yamada, Koyo, Nakajima, Yuto, Ogiwara, Kenichi, Sakai, Toshiyuki, Fukuda, Kazuyoshi, Nogami, Keiji

    Published in Pediatrics international (01-01-2024)
    “…Lupus anticoagulant-hypoprothrombinemia syndrome (LAHPS) is a rare disease caused by acquired factor II (FII) deficiency and lupus anticoagulant. Patients with…”
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    Anesthetic management of a patient with congenital plasminogen activator inhibitor-1 deficiency by Kajihara, Atsuhisa, Kurehara, Hiroyoshi, Kitaguchi, Katsuyasu, Furuya, Hitoshi, Morimoto, Yoshinari, Kirita, Tadaaki, Fukuda, Kazuyoshi, Takahashi, Yukihiro

    “…Congenital plasminogen activator inhibitor-1 (PAI-1) deficiency is an extremely rare disorder characterized by a bleeding diathesis due to hyperfibrinolysis as…”
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    Association of anti-idiotypic antibodies with immune tolerance induction for the treatment of hemophilia A with inhibitors by Sakurai, Y, Shima, M, Tanaka, I, Fukuda, K, Yoshida, K, Yoshioka, A

    Published in Haematologica (Roma) (01-06-2004)
    “…Department of Pediatrics, Nara Medical University, Nara, Japan. ysakurai@naramed-u.ac.jp BACKGROUND AND OBJECTIVES: Hemophilia A patients with inhibitors can…”
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    A 4-year-old girl with autosomal dominant polycystic kidney disease complicated by a ruptured intracranial aneurysm by KUBO, Satomi, NAKAJIMA, Mitsuru, FUKUDA, Kazuyoshi, NOBAYASHI, Misato, SAKAKI, Toshisuke, AOKI, Katsuya, HIRAO, Yoshihiko, YOSHIOKA, Akira

    Published in European journal of pediatrics (01-11-2004)
    “…In patients with autosomal dominant polycystic kidney disease (ADPKD), intracranial aneurysms (ICAs) are extrarenal manifestations and may result in serious…”
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    Pb-210, Bi-210, and Po-210 in meteoric precipitation and the residence time of tropospheric aerosol by Tsunogai, Shizuo, Fukuda, Kazuyoshi

    Published in GEOCHEMICAL JOURNAL (1974)
    “…The concentrations of 210Pb, 210Bi and 210Po in rain and snow were determined. Extremely high concentrations of 210Pb, e.g. 190dpm/l, were observed for snow…”
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  17. 17

    Immunological Characterization of Factor VIII Autoantibodies in Patients with Acquired Hemophilia A in the Presence or Absence of Underlying Disease by Matsumoto, Tomoko, Shima, Midori, Fukuda, Kazuyoshi, Nogami, Keiji, Giddings, John C, Murakami, Tomohiko, Tanaka, Ichiro, Yoshioka, Akira

    Published in Thrombosis research (15-12-2001)
    “…The development of a factor VIII autoantibody results in a severe hemorrhagic diathesis known as acquired hemophilia A. Underlying pathologies, such as…”
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