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Journal Articles

Association of Neurodevelopmental Abnormalities Is a Common Clinical Character in Japanese Patients with Severe Congenital Neutropenia Due to HAX1 Deficiency.

Satoshi Okada, MD, Nobutsune Ishikawa, M.D., Kenichiro Shirao, M.D., Miyuki Tsumura, M.Sc., Takashi Satoh, M.D., Yoshinori Ohno, M.Sc., Shin’ichiro Yasunaga, Ph.D., Motoaki Ohtsubo, Ph.D., Yoshihiro Takihara, Ph.D., Masao Kobayashi, M.D.

Blood (2007) 110 (11): 665.

https://doi.org/10.1182/blood.V110.11.665.665

Published: 2007

Journal Articles

Abnormal Localization of Neutrophil Elastase in Patients with Severe Congenital Neutropenia.

Takashi Sato, MD, Masakazu Habara, MD, Hiroki Kihara, MD, Hiroshi Kawaguchi, MD, Mizuka Miki, MD, Kazuhiro Nakamura, MD, Satoshi Okada, MD, Nobutsune Ishikawa, MD, Norioki Ohno, MD, Masao Kobayashi

Blood (2006) 108 (11): 1279.

https://doi.org/10.1182/blood.V108.11.1279.1279

Published: 2006

Journal Articles

A Novel Mutation 774del4 in IFNGR1 , Which Produces Truncated Form of Interferon γ Receptor 1, Causes a Dominant-Negative Effect on Interferon γ Signal Transduction.

Satoshi Okada, MD, Nobutsune Ishikawa, M.D., Kenichirou Shirao, M.D., Hiroshi Kawaguchi, M.D., Miyuki Tsumura, Ph.D., Yoshinori Ohno, Ph.D., Shin’ichiro Yasunaga, Ph.D., Motoaki Ohtsubo, Ph.D., Yoshihiro Takihara, Ph.D., Masao Kobayashi, M.D.

Blood (2006) 108 (11): 1246.

https://doi.org/10.1182/blood.V108.11.1246.1246

Published: 2006

Journal Articles

Compound Heterozygosity for a Novel Mutation Combined with G Insertion in Exon 13 Causes Severe Factor XI Deficiency in Patients of Japanese Origin.

Nobutsune Ishikawa, Shinichiro Yasunaga, Motoaki Ohtsubo, Yoshihiro Takihara, Takashi Sato, Masao Kobayashi

Blood (2005) 106 (11): 4087.

https://doi.org/10.1182/blood.V106.11.4087.4087

Published: 2005

Journal Articles

Neutrophil Elastase Modulates Granulopoiesis through the Interaction of G-CSF and G-CSF Receptor.

Takashi Sato, MD, Masakazu Habara, MD, Hiroki Kihara, MD, Hiroshi Kawaguchi, MD, Kazuhiro Nakamura, MD, Satoshi Okada, MD, Nobutsune Ishikawa, MD, Norioki Ohno, MD, Masao Kobayashi, MD

Blood (2005) 106 (11): 3066.

https://doi.org/10.1182/blood.V106.11.3066.3066

Published: 2005

NARROW

Association of Neurodevelopmental Abnormalities Is a Common Clinical Character in Japanese Patients with Severe Congenital Neutropenia Due to HAX1 Deficiency.

Abnormal Localization of Neutrophil Elastase in Patients with Severe Congenital Neutropenia.

A Novel Mutation 774del4 in IFNGR1 , Which Produces Truncated Form of Interferon γ Receptor 1, Causes a Dominant-Negative Effect on Interferon γ Signal Transduction.

Compound Heterozygosity for a Novel Mutation Combined with G Insertion in Exon 13 Causes Severe Factor XI Deficiency in Patients of Japanese Origin.

Neutrophil Elastase Modulates Granulopoiesis through the Interaction of G-CSF and G-CSF Receptor.

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ASH Publications

American Society of Hematology

Association of Neurodevelopmental Abnormalities Is a Common Clinical Character in Japanese Patients with Severe Congenital Neutropenia Due to HAX1 Deficiency.

Abnormal Localization of Neutrophil Elastase in Patients with Severe Congenital Neutropenia.

A Novel Mutation 774del4 in IFNGR1 , Which Produces Truncated Form of Interferon γ Receptor 1, Causes a Dominant-Negative Effect on Interferon γ Signal Transduction.

Compound Heterozygosity for a Novel Mutation Combined with G Insertion in Exon 13 Causes Severe Factor XI Deficiency in Patients of Japanese Origin.

Neutrophil Elastase Modulates Granulopoiesis through the Interaction of G-CSF and G-CSF Receptor.

Email alerts

ASH Publications

American Society of Hematology

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