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Journal Articles

Molecular Diagnosis of Hemophilia B Leyden in Japanese Brothers Reveals Spontaneous Amelioration in Early Childhood with c. -35 G>A Onecut Binding Site Mutation

Akihiro Tamura, MD, Daiichiro Hasegawa, MD PhD, Sayaka Nakamura, MD, Takahiro Fujiwara, MD, Teppei Tahara, MD, Nobuyuki Yamamoto, MD PhD, Atsuro Saito, MD, Aiko Kozaki, MD, Kenji Kishimoto, MD, Toshiaki Ishida, MD PhD, Keiko Shinozawa, PhD, Kagehiro Amano, MD PhD, Katsuyuki Fukutake, MD PhD, Yoshiyuki Kosaka, MD, PhD

Blood (2017) 130 (Supplement 1): 3680.

https://doi.org/10.1182/blood.V130.Suppl_1.3680.3680

Published: 2017

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

Mechanism of the Potent Activated Protein C Resistance of Novel Factor V Mutation with W1920R (FV Nara) Relative to R506Q (FV Leiden)

Kenichi Ogiwara, MD, PhD, Keiko Shinozawa, PhD, Keiji Nogami, MD, PhD, Tomoko Matsumoto, Katsumi Nishiya, MD, PhD, Nobuyuki Tsujii, MD, Koji Yada, MD, Katsuyuki Fukutake, MD, PhD, Midori Shima, MD, PhD

Blood (2011) 118 (21): 537.

https://doi.org/10.1182/blood.V118.21.537.537

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

Molecular Diagnosis of Hemophilia B Leyden in Japanese Brothers Reveals Spontaneous Amelioration in Early Childhood with c. -35 G>A Onecut Binding Site Mutation

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

Mechanism of the Potent Activated Protein C Resistance of Novel Factor V Mutation with W1920R (FV Nara) Relative to R506Q (FV Leiden)

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

Molecular Diagnosis of Hemophilia B Leyden in Japanese Brothers Reveals Spontaneous Amelioration in Early Childhood with c. -35 G>A Onecut Binding Site Mutation

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

Mechanism of the Potent Activated Protein C Resistance of Novel Factor V Mutation with W1920R (FV Nara) Relative to R506Q (FV Leiden)

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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