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Journal Articles

Successful Reduced-Intensity Stem Cell Transplantation From Unrelated Cord Blood In Three Patients with X-Linked Severe Combined Immunodeficiency.

Akihiro Iguchi, MD, PhD, Mizuho Ichikawa, MD, PhD, Nobuaki Kawamura, MD, PhD, Shunichiro Takezaki, MD, Yuka Okura, MD, Jun Inamoto, MD, Junjiro Ohshima, MD, PhD, Tomonobu Sato, MD, PhD, Masahide Nakajima, MD, PhD, Makoto Kaneda, MD, Yuko Cho, MD, PhD, Masafumi Yamada, MD, PhD, Ryoji Kobayashi, MD, PhD, Ichiro Kobayashi, MD, PhD, Tadashi Ariga, MD, PhD

Blood (2010) 116 (21): 4571.

https://doi.org/10.1182/blood.V116.21.4571.4571

Published: 2010

Journal Articles

Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression

Koji Yamaguchi, Tadashi Ariga, Masafumi Yamada, David L. Nelson, Ryouji Kobayashi, Chie Kobayashi, Yasushi Noguchi, Yasuhiko Ito, Kenji Katamura, Yoshihisa Nagatoshi, Satoshi Kondo, Hiroyuki Katoh, Yukio Sakiyama

Blood (2002) 100 (4): 1208–1214.

https://doi.org/10.1182/blood-2002-01-0211

Published: 2002

Journal Articles

Flow Cytometric Analysis of Wiskott-Aldrich Syndrome (WAS) Protein in Lymphocytes From WAS Patients and Their Familial Carriers

Masafumi Yamada, Makoto Ohtsu, Ichiro Kobayashi, Nobuaki Kawamura, Kunihiko Kobayashi, Tadashi Ariga, Yukio Sakiyama, David L. Nelson, Satoshi Tsuruta, Michiya Anakura, Nobuyoshi Ishikawa

Blood (1999) 93 (2): 756–758.

https://doi.org/10.1182/blood.V93.2.756

Published: 1999

Journal Articles

A Case of Wiskott-Aldrich Syndrome With Dual Mutations in Exon 10 of the WASP Gene: An Additional De Novo One-Base Insertion, Which Restores Frame Shift Due to an Inherent One-Base Deletion, Detected in the Major Population of the Patient's Peripheral Blood Lymphocytes

Tadashi Ariga, Masafumi Yamada, Yukio Sakiyama, Osamu Tatsuzawa

Blood (1998) 92 (2): 699–701.

https://doi.org/10.1182/blood.V92.2.699

Published: 1998

Journal Articles

Successful Peripheral T-Lymphocyte–Directed Gene Transfer for a Patient With Severe Combined Immune Deficiency Caused by Adenosine Deaminase Deficiency

Masafumi Onodera, Tadashi Ariga, Nobuaki Kawamura, Ichiro Kobayashi, Makoto Ohtsu, Masafumi Yamada, Atsushi Tame, Hirofumi Furuta, Motohiko Okano, Shuzo Matsumoto, Hitoshi Kotani, Gerard J. McGarrity, R. Michael Blaese, Yukio Sakiyama

Blood (1998) 91 (1): 30–36.

https://doi.org/10.1182/blood.V91.1.30

Published: 1998

NARROW

Successful Reduced-Intensity Stem Cell Transplantation From Unrelated Cord Blood In Three Patients with X-Linked Severe Combined Immunodeficiency.

Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression

Flow Cytometric Analysis of Wiskott-Aldrich Syndrome (WAS) Protein in Lymphocytes From WAS Patients and Their Familial Carriers

A Case of Wiskott-Aldrich Syndrome With Dual Mutations in Exon 10 of the WASP Gene: An Additional De Novo One-Base Insertion, Which Restores Frame Shift Due to an Inherent One-Base Deletion, Detected in the Major Population of the Patient's Peripheral Blood Lymphocytes

Successful Peripheral T-Lymphocyte–Directed Gene Transfer for a Patient With Severe Combined Immune Deficiency Caused by Adenosine Deaminase Deficiency

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ASH Publications

American Society of Hematology

Successful Reduced-Intensity Stem Cell Transplantation From Unrelated Cord Blood In Three Patients with X-Linked Severe Combined Immunodeficiency.

Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression

Flow Cytometric Analysis of Wiskott-Aldrich Syndrome (WAS) Protein in Lymphocytes From WAS Patients and Their Familial Carriers

A Case of Wiskott-Aldrich Syndrome With Dual Mutations in Exon 10 of the WASP Gene: An Additional De Novo One-Base Insertion, Which Restores Frame Shift Due to an Inherent One-Base Deletion, Detected in the Major Population of the Patient's Peripheral Blood Lymphocytes

Successful Peripheral T-Lymphocyte–Directed Gene Transfer for a Patient With Severe Combined Immune Deficiency Caused by Adenosine Deaminase Deficiency

Email alerts

ASH Publications

American Society of Hematology

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