K. Shinozawa

发表

Genotypic and phenotypic features of Japanese patients with mild to moderate hemophilia A

K. Amano, K. Fukutake, H. Inaba, 2013, International journal of hematology.

Coagulation assay discrepancies in Japanese patients with non-severe hemophilia A

S. Nishikawa, S. Nishikawa, K. Amano, 2021, International Journal of Hematology.

Emicizumab‐mediated haemostatic function in patients with haemophilia A is down‐regulated by activated protein C through inactivation of activated factor V

K. Nogami, K. Amano, M. Shima, 2018, British journal of haematology.

Identification and characterization of an adenine to guanine transition within intron 10 of the factor VIII gene as a causative mutation in a patient with mild haemophilia A

K. Amano, K. Fukutake, H. Inaba, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Genotyping analysis of the factor V Nara mutation, Hong Kong mutation, and 16 single-nucleotide polymorphisms, including the R2 haplotype, and the involvement of factor V activity in patients with recurrent miscarriage

K. Fukutake, M. Sugiura-Ogasawara, Y. Ozaki, 2017, Blood Coagulation and Fibrinolysis.

Novel FV mutation (W1920R, FVNara) associated with serious deep vein thrombosis and more potent APC resistance relative to FVLeiden.

Tomoko Matsumoto, K. Nogami, K. Amano, 2014, Blood.

Molecular characterization of 3 factor V mutations, R2174L, V1813M, and a 5-bp deletion, that cause factor V deficiency

K. Amano, K. Fukutake, H. Inaba, 2007 .

IgG antibodies against polyethylene glycol (PEG) in patient with hemophilia A

K. Amano, H. Inaba, E. Kinai, 2021, Japanese Journal of Thrombosis and Hemostasis.

[Inhibitory effect of ulinastatin on the alpha-thrombin activation of factors V and VIII].

K. Fukutake, K. Shinozawa, T. Kobayashi, 1992, Rinsho byori. The Japanese journal of clinical pathology.

Prolonged α-thrombin-related activation and delayed active protein C-associated degradation confer mild phenotype in a patient with severe hemophilia A with F8 p.H118R

K. Amano, H. Inaba, E. Kinai, 2022, International Journal of Hematology.

[Examination of the effect of immunosuppressive therapy on acquired hemophilia A in elderly patients with bloodstream infections].

A. Gotoh, K. Amano, Mitsuru Moriyama, 2022, Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics.

Development of asymptomatic acquired factor V inhibitor after the administration of antibiotics.

Kazuaki Yoshimura, K. Shinozawa, Takashi Suzuki, 2014, [Rinsho ketsueki] The Japanese journal of clinical hematology.

In vitro validation of chromogenic substrate assay for evaluation of surrogate FVIII-activity of emicizumab.

S. Nagatoishi, K. Amano, H. Inaba, 2023, Thrombosis research.

Genetic analysis of carrier status in female members of Japanese hemophilia families

K. Amano, K. Fukutake, H. Inaba, 2021, Journal of thrombosis and haemostasis : JTH.

Clinical conditions and risk factors for inhibitor‐development in patients with haemophilia: A decade‐long prospective cohort study in Japan, J‐HIS2 (Japan Hemophilia Inhibitor Study 2)

J. Takamatsu, S. Ohga, Masao Kobayashi, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Causative mutation and single nucleotide polymorphisms associated with inhibitor development in patients with hemophilia

K. Shinozawa, 2012 .

Early elevation of factor IX level in japanese brothers with Haemophilia B Leyden who are carrying c. ‐35 g > a mutations in the promoter region of F9

K. Amano, K. Fukutake, T. Muramatsu, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic analysis is valuable for diagnostic testing for carrier status with hemophilia

K. Shinozawa, 2015 .

The Prevalence of Co-infection with Hepatitis Viruses in Human Immunodeficiency Virus (HIV) Infected Patients in Japan and the Efficacy of Hepatitis B Virus (HBV) /Hepatitis A Virus (HAV) Vaccination

K. Amano, K. Fukutake, M. Ohtaki, 2007 .

A novel synonymous variant in the F8 gene, p.(Leu40=)/c.120C>A, likely causes mild haemophilia A

K. Amano, K. Fukutake, H. Inaba, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of deep intronic individual variants in patients with hemophilia A by next‐generation sequencing of the whole factor VIII gene

K. Amano, K. Fukutake, H. Inaba, 2017, Research and practice in thrombosis and haemostasis.

Features of factor VIII activity measurement in Arg531His mutant detected in patients with mild hemophilia A

Y. Yatomi, K. Amano, K. Fukutake, 2008 .

Combination therapy with von Willebrand factor concentrate plus recombinant factor VIII during cesarean section in a patient with type 3 von Willebrand disease and a low inhibitor titer: a case report

K. Amano, K. Fukutake, E. Kinai, 2022, International Journal of Hematology.

Factor X M402T: a homozygous missense mutation identified as the cause of cross-reacting material-reduced deficiency

K. Amano, K. Fukutake, H. Inaba, 2014, International Journal of Hematology.

Spectrum of F8 Genotype and Genetic Impact on Inhibitor Development in Patients with Hemophilia A from Multicenter Cohort Studies (J-HIS) in Japan

A. Shirahata, K. Nogami, M. Taki, 2020, Thrombosis and Haemostasis.

Successful Management of Acquired Factor V Inhibitor by Monitoring Factor V Activity, Antigen, and Inhibitor Values during Immunosuppressive Therapy

K. Fukutake, Y. Ogawa, H. Handa, 2019, Acta Haematologica.

Factor VIII haplotypes of Japanese population show similarity to those of Caucasian populations

K. Amano, K. Fukutake, H. Inaba, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Two cases of acquired factor V inhibitor which were initially diagnosed with congenital deficiency by cross mixing tests

K. Amano, K. Fukutake, H. Inaba, 2018 .

Molecular characterization of 3 factor V mutations, R2174L, V1813M, and a 5-bp deletion, that cause factor V deficiency.

K. Amano, K. Fukutake, H. Inaba, 2007, International journal of hematology.

ANALYSIS OF DISCREPANT ASSAY-DETERMINED ACTIVITY LEVELS OF FACTOR VIII ASSOCIATED WITH R531H MUTATION

Y. Yatomi, K. Amano, K. Fukutake, 2007 .

Clinical evaluation of D-dimer testing in disseminated intravascular coagulation (DIC)

K. Fukutake, K. Shinozawa, K. Kuroso, 1993 .