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Keiko Shinozawa

Tokyo Medical University

H指数:9

被引数:301

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Assay Discrepancy in Factor IX Activity in Haemophilia B and the Unique Assay Characteristics of FIX: p.Ala74Pro

血友病B中因子IX活性测定差异及FIX：p.Ala74Pro的独特测定特征

IF3

2025-05-270

PRE

Trisomy X conferring moderate hemophilia A by extremely skewed X-chromosome inactivation

RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS

IF3.4

2023-10-011

OAAI

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

THROMBOSIS RESEARCH

IF3.4

2023-02-014

OAAI

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)

IF3

2022-06-113

PRE

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

JOURNAL OF THROMBOSIS AND HAEMOSTASIS

IF5

2021-06-015

OAAI

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

IF3

2021-01-112

PREAI

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

THROMBOSIS AND HAEMOSTASIS

IF4.3

2020-11-308

PREAI

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

IF3

2018-07-130

PREAI

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

RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS

IF3.4

2017-10-0119

OAAI

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

IF3

2012-07-0928

OAAI

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

IF3

2011-12-192

PREAI