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High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome

Leukemia, 2006-04, Vol.20 (4), p.627-634

2006

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Investigation on apoptosis in paroxysmal nocturnal hemoglobinuria (PNH) granulocytes

Rinsho byori. The Japanese journal of clinical pathology, 2001-10, Vol.49 (10), p.986

Shichishima, T

2001

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Paroxysmal nocturnal hemoglobinuria: pathogenesis and diversity of clinical manifestations

Rinshō ketsueki, 2001-02, Vol.42 (2), p.68

Shichishima, T

2001

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P-63 Effects of alternative splicing and nonsense-mediated mRNA decay on the expression of a variant of GM-CSF receptor beta chain in myelodysplastic syndromes

Leukemia research, 2005, Vol.29, p.S48-S48

2005

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Complement sensitivity of erythrocytes in a patient with inherited complete deficiency of CD59 or with the Inab phenotype

British journal of haematology, 1999-02, Vol.104 (2), p.303-306

1999

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Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan

Medicine (Baltimore), 2004-05, Vol.83 (3), p.193-207

2004

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P-51 Phosphatidylinositol glycan-class a (PIG-A) gene mutations in patients with aplastic anemia (AA) and myelodysplastic syndrome (MDS)

Leukemia research, 2005, Vol.29, p.S43-S44

2005

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Prospective measurement of Epstein-Barr virus–DNA in plasma and peripheral blood mononuclear cells of extranodal NK/T-cell lymphoma, nasal type

Blood, 2011-12, Vol.118 (23), p.6018-6022

2011

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Diagnosis and therapy of paroxysmal nocturnal hemoglobinuria

Nihon Naika Gakkai zasshi, 1999-06, Vol.88 (6), p.1022-1028

1999

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The frequency of HLA class I alleles in Japanese patients with bone marrow failure

Haematologica (Roma), 2006-06, Vol.91 (6), p.856-857

2006

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PS1115 THE RELATIONSHIP BETWEEN THE PRETREATMENT PNH CLONE SIZE AND CLINICAL COURSE IN PATIENTS WITH BONE MARROW FAILURE SYNDROMES: INTERIM ANALYSIS OF JAPANESE MULTICENTER PROSPECTIVE STUDY

HemaSphere, 2019-06, Vol.3 (S1), p.504-505

2019

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Glycosylphosphatidylinositol (GPI)-anchored membrane proteins in clinical pathophysiology of paroxysmal nocturnal hemoglobinuria (PNH)

Fukushima journal of medical science, 1995-06, Vol.41 (1), p.1

Shichishima, T

1995

Volltextzugriff (PDF)

Complement sensitivity of erythroblasts and erythropoietic precursors in paroxysmal nocturnal haemoglobinuria (PNH)

British journal of haematology, 1989-08, Vol.72 (4), p.578-583

1989

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Collection of MNCs and progenitor cells by two separators for PBPC transplantation: a randomized crossover trial

Transfusion (Philadelphia, Pa.), 2003-06, Vol.43 (6), p.814-819

2003

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HLA class II haplotype and quantitation of WT1 RNA in Japanese patients with paroxysmal nocturnal hemoglobinuria

Blood, 2002-07, Vol.100 (1), p.22-28

2002

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Effective treatment combining antithymocyte globulin, cyclosporin A, and granulocyte colony-stimulating factor for atypical paroxysmal nocturnal hemoglobinuria accompanied by bone marrow hypoplasia

Rinshō ketsueki, 1999-03, Vol.40 (3), p.240

1999

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Myositis caused by hydroxyurea in a patient with chronic myelogenous leukemia

Rinshō ketsueki, 1998-09, Vol.39 (9), p.676

1998

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Myelodysplastic syndrome with multiple chromosome aberrations in a patient with Werner's syndrome

Rinshō ketsueki, 1996-08, Vol.37 (8), p.725

1996

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Immune thrombocytopenia in an elderly patient treated successfully by pulse therapy with cyclophosphamide

Fukushima journal of medical science, 2001, Vol.47 (1), p.33-38

2001

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Fatal pulmonary thromboembolism in a patient with paroxysmal nocturnal hemoglobinuria

Rinshō ketsueki, 1998-02, Vol.39 (2), p.150

1998

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Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation

Blood, 2001-05, Vol.97 (9), p.2667-2672

2001

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Complete donor chimaerism of Langerhans cells in lymph node early after allogeneic bone marrow transplantation

European journal of haematology, 2006-03, Vol.76 (3), p.261-264

2006

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Minimally Differentiated Erythroleukemia: Recognition of Erythroid Precursors and Progenitors

Internal Medicine, 2000, Vol.39(10), pp.761-762

SHICHISHIMA, Tsutomu

2000

Volltextzugriff (PDF)

Surface expression of complement regulatory proteins, decay-accelerating factor (DAF) and CD59, on cultured human endothelial cells

Fukushima journal of medical science, 1998-12, Vol.44 (2), p.69

1998

Volltextzugriff (PDF)

Sweet's syndrome in a patient with chronic myeloproliferative disorder during recombinant human granulocyte colony stimulating factor therapy

Rinshō ketsueki, 1995-04, Vol.36 (4), p.353

1995

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High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome

Investigation on apoptosis in paroxysmal nocturnal hemoglobinuria (PNH) granulocytes

Paroxysmal nocturnal hemoglobinuria: pathogenesis and diversity of clinical manifestations

P-63 Effects of alternative splicing and nonsense-mediated mRNA decay on the expression of a variant of GM-CSF receptor beta chain in myelodysplastic syndromes

Complement sensitivity of erythrocytes in a patient with inherited complete deficiency of CD59 or with the Inab phenotype

Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan

P-51 Phosphatidylinositol glycan-class a (PIG-A) gene mutations in patients with aplastic anemia (AA) and myelodysplastic syndrome (MDS)

Prospective measurement of Epstein-Barr virus–DNA in plasma and peripheral blood mononuclear cells of extranodal NK/T-cell lymphoma, nasal type

Diagnosis and therapy of paroxysmal nocturnal hemoglobinuria

The frequency of HLA class I alleles in Japanese patients with bone marrow failure

PS1115 THE RELATIONSHIP BETWEEN THE PRETREATMENT PNH CLONE SIZE AND CLINICAL COURSE IN PATIENTS WITH BONE MARROW FAILURE SYNDROMES: INTERIM ANALYSIS OF JAPANESE MULTICENTER PROSPECTIVE STUDY

Glycosylphosphatidylinositol (GPI)-anchored membrane proteins in clinical pathophysiology of paroxysmal nocturnal hemoglobinuria (PNH)

Complement sensitivity of erythroblasts and erythropoietic precursors in paroxysmal nocturnal haemoglobinuria (PNH)

Collection of MNCs and progenitor cells by two separators for PBPC transplantation: a randomized crossover trial

HLA class II haplotype and quantitation of WT1 RNA in Japanese patients with paroxysmal nocturnal hemoglobinuria

Effective treatment combining antithymocyte globulin, cyclosporin A, and granulocyte colony-stimulating factor for atypical paroxysmal nocturnal hemoglobinuria accompanied by bone marrow hypoplasia

Myositis caused by hydroxyurea in a patient with chronic myelogenous leukemia

Myelodysplastic syndrome with multiple chromosome aberrations in a patient with Werner's syndrome

Immune thrombocytopenia in an elderly patient treated successfully by pulse therapy with cyclophosphamide

Fatal pulmonary thromboembolism in a patient with paroxysmal nocturnal hemoglobinuria

Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation

Complete donor chimaerism of Langerhans cells in lymph node early after allogeneic bone marrow transplantation

Minimally Differentiated Erythroleukemia: Recognition of Erythroid Precursors and Progenitors

Surface expression of complement regulatory proteins, decay-accelerating factor (DAF) and CD59, on cultured human endothelial cells

Sweet's syndrome in a patient with chronic myeloproliferative disorder during recombinant human granulocyte colony stimulating factor therapy

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