T. Hagiwara

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.

Chronic kidney disease is related to femoral neck bone loss among HIV-1-infected patients : a retrospective study

T. Muramatsu, K. Amano, K. Fukutake, 2019 .

Acute alveolar haemorrhage in a patient with haemophilia B

K. Amano, K. Fukutake, I. Seita, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of Two Point Mutations in Japanese Patients with Congenital Coagulation Factor XIII A Subunit Deficiencies

S. Yoshida, M. Shima, K. Fukutake, 1998 .

Long-term administration of pegylated liposomal doxorubicin at almost twice the recommended lifetime dose in 10 years without cardiotoxicity in a Japanese patient with HIV-associated Kaposi sarcoma.

K. Amano, K. Fukutake, T. Muramatsu, 2020, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Identification of Missense Mutations in the FVII Gene of Three FVII Deficiencies

K. Amano, K. Fukutake, H. Inaba, 2001 .

The Hemostatic Management by Continuous Infusion of Monoclonal Antibody-Purified Factor VIII Concentrate in the Treatment of Patients with Hemophilia A

S. Yoshida, K. Amano, K. Fukutake, 1996 .

Beta interferon therapy for chronic hepatitis C in patients with haemophilia and other haemorrhagic disorders

K. Fukutake, T. Yamagishi, T. Hagiwara, 1996, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

Inversion in Japanese Patients with Hemophilia A

K. Fukutake, H. Inaba, T. Nagao, 1995, Thrombosis and Haemostasis.

Two double heterozygous mutations in the F7 gene show different manifestations

K. Amano, K. Fukutake, Y. Hatta, 2002, British journal of haematology.

A Novel Mutation Glyl672→Arg in Type 2A and a Homozygous Mutation in Type 2B von Willebrand Disease

S. Yoshida, K. Fukutake, H. Inaba, 1996, Thrombosis and Haemostasis.

Identification of a Novel Point Mutation (Ala94 to Val) in a Hereditary Type I Antithrombin III Deficiency

S. Yoshida, K. Fukutake, H. Inaba, 1996 .

Management of a Patient with Factor XI Deficiency in Total Hip Joint Replacement by Plasma Exchange Transfusion

Kengo Yamamoto, K. Amano, K. Fukutake, 1995 .

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.

Gardner–Diamond syndrome complicated with chronic urticaria successfully treated with antihistamine

T. Hagiwara, K. Harada, 2021, The Journal of dermatology.

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.

Young age is a key determinant of body weight gain after switching from tenofovir disoproxil fumarate to tenofovir alafenamide in Japanese people living with HIV

K. Amano, T. Muramatsu, E. Kinai, 2022, Journal of Infection and Chemotherapy.

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 .