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Journal Articles

Differentiation of Acquired Hemophilia a from Lupus Anticoagulant Using Global Coagulation Assays and Magnesium-Dependent Activated Partial Thromboplastin Time Assay

Yushi Chikasawa, Kagehiro Amano, Keiko Shinozawa, Masato Bingo, Ryui Miyashita, Tomoko Yamaguchi, Akito Ichiki, Ryoko Sekiya, Takashi Muramatsu, Mihoko Yotsumoto, Ayano Mitsuhashi, Takeshi Hagiwara, Hiroshi Inaba, Ei Kinai

Blood (2023) 142 (Supplement 1): 5463.

https://doi.org/10.1182/blood-2023-179884

Published: 2023

Journal Articles

The Genetic Analysis of Hemophilia a: The Application of Next-Generation Sequencing in the Analysis of Causative Variants Deep inside the Intron of the F8 Gene

Hiroshi Inaba, PhD, Keiko Shinozawa, PhD, Kagehiro Amano, MD PhD, Katsuyuki Fukutake, MD PhD

Blood (2016) 128 (22): 1393.

https://doi.org/10.1182/blood.V128.22.1393.1393

Published: 2016

Journal Articles

Severe Factor V Deficiency Caused by a Novel Compound Heterozygous Mutation: Factor V G1617V and 1-Bp Insertion

Keiko Shinozawa, PhD, Yuri Okimoto, MD, PhD, Kagehiro Amano, MD, PhD, Harumi Kakuda, MD, PhD, Takeshi Hagiwara, MD, PhD, Takashi Suzuki, MD, PhD, Hiroshi Inaba, PhD, Katsuyuki Fukutake, MD, PhD

Blood (2011) 118 (21): 2268.

https://doi.org/10.1182/blood.V118.21.2268.2268

Published: 2011

Journal Articles

The Etiology of Hemophilia Hiding Deep Inside the F8 Intronic Sequence

Hiroshi Inaba, PhD, Keiko Shinozawa, PhD, Takeshi Hagiwara, MD, PhD, Kagehiro Amano, MD, PhD, Katsuyuki Fukutake, MD, PhD

Blood (2011) 118 (21): 1223.

https://doi.org/10.1182/blood.V118.21.1223.1223

Published: 2011

Journal Articles

Identification and Characterization of L1-Mediated Large Tandem Duplication, Spanning Exon 4 to 10 of the F13A1 , In a Patient with Congenital Factor XIII Deficiency.

Hiroshi Inaba, PhD, Keiko Shinozawa, PhD, Kagehiro Amano, MD, PhD, Katsuyuki Fukutake, MD, PhD

Blood (2010) 116 (21): 3659.

https://doi.org/10.1182/blood.V116.21.3659.3659

Published: 2010

Journal Articles

The Severity of Bleeding Tendency in 5 Patients with Factor V Deficiency Due to Distinct Kinds of Factor V Mutations.

Keiko Shinozawa, PhD, Kagehiro Amano, MD, PhD, Takashi Suzuki, MD, PhD, Hiroshi Inaba, PhD, Katsuyuki Fukutake, MD, PhD

Blood (2007) 110 (11): 1764.

https://doi.org/10.1182/blood.V110.11.1764.1764

Published: 2007

NARROW

Differentiation of Acquired Hemophilia a from Lupus Anticoagulant Using Global Coagulation Assays and Magnesium-Dependent Activated Partial Thromboplastin Time Assay

The Genetic Analysis of Hemophilia a: The Application of Next-Generation Sequencing in the Analysis of Causative Variants Deep inside the Intron of the F8 Gene

Severe Factor V Deficiency Caused by a Novel Compound Heterozygous Mutation: Factor V G1617V and 1-Bp Insertion

The Etiology of Hemophilia Hiding Deep Inside the F8 Intronic Sequence

Identification and Characterization of L1-Mediated Large Tandem Duplication, Spanning Exon 4 to 10 of the F13A1 , In a Patient with Congenital Factor XIII Deficiency.

The Severity of Bleeding Tendency in 5 Patients with Factor V Deficiency Due to Distinct Kinds of Factor V Mutations.

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ASH Publications

American Society of Hematology

Differentiation of Acquired Hemophilia a from Lupus Anticoagulant Using Global Coagulation Assays and Magnesium-Dependent Activated Partial Thromboplastin Time Assay

The Genetic Analysis of Hemophilia a: The Application of Next-Generation Sequencing in the Analysis of Causative Variants Deep inside the Intron of the F8 Gene

Severe Factor V Deficiency Caused by a Novel Compound Heterozygous Mutation: Factor V G1617V and 1-Bp Insertion

The Etiology of Hemophilia Hiding Deep Inside the F8 Intronic Sequence

Identification and Characterization of L1-Mediated Large Tandem Duplication, Spanning Exon 4 to 10 of the F13A1 , In a Patient with Congenital Factor XIII Deficiency.

The Severity of Bleeding Tendency in 5 Patients with Factor V Deficiency Due to Distinct Kinds of Factor V Mutations.

Email alerts

ASH Publications

American Society of Hematology

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