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Bone marrow transplantation for patients with chronic myeloid leukaemia: T-cell depletion with Campath-1 reduces the incidence of graft-versus-host disease but may increase the risk of leukaemic relapse

Bone marrow transplantation (Basingstoke), 1986-05, Vol.1 (1), p.53-66

1986

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Angioid Streaks in Sickle-Thalassemia

American journal of ophthalmology, 1994-05, Vol.117 (5), p.589-592

1994

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Hemothorax due to extramedullary erythropoietic masses

The Annals of thoracic surgery, 2004, Vol.77 (1), p.323-324

2004

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Transfusion‐induced hypoxemia in beta‐thalassaemia

American journal of hematology, 1996-11, Vol.53 (3), p.206-206

1996

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Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report

Minerva pediatrica, 2008-08, Vol.60 (4), p.469

2008

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Erythropoietin levels and microcytosis in heterozygous beta-thalassaemia

Acta haematologica, 1997, Vol.98 (3), p.147

1997

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The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients

Haematologica (Roma), 2004-04, Vol.89 (4), p.490

2004

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Development of plasma cell tumors during treatment of multiple myeloma

Annals of hematology, 1996-05, Vol.72 (5), p.317-320

1996

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Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease

Blood cells, molecules, & diseases, 2003-07, Vol.31 (1), p.38-42

2003

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Chelation therapy in patients with thalassemia using the orally active iron chelator deferiprone (L1)

Haematologica (Roma), 2000-02, Vol.85 (2), p.115

2000

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Evaluation of the clinical relevance of the expression and function of P-glycoprotein, multidrug resistance protein and lung resistance protein in patients with primary acute myelogenous leukemia

Leukemia research, 2002-02, Vol.26 (2), p.143-154

2002

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Spleen size in beta-thalassaemia heterozygotes

Haematologia, 1995, Vol.26 (4), p.205

1995

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Randomized clinical trial comparing ceftriaxone/amikacin versus ceftazidime/amikacin as initial therapy of febrile episodes in neutropenic patients

Chemotherapy (Basel), 1991, Vol.37 (5), p.376

1991

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Amelioration of Painful Crises in Sickle Cell Disease by Venesections

Blood cells, molecules, & diseases, 2002-03, Vol.28 (2), p.283-287

2002

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Immunological reconstitution after bone marrow transplant with Campath-1 treated bone marrow

Clinical and experimental immunology, 1987, Vol.67 (1), p.142-150

1987

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HIV infection due to a platelet transfusion after allogeneic bone marrow transplantation

European journal of haematology, 1987-08, Vol.39 (2), p.185-189

1987

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Multiple myeloma in sickle cell syndromes

Haematologia, 2001-01, Vol.31 (2), p.153

2001

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Detection of "PNH Red Cell" Populations in Hematological Disorders Using the Sephacryl Gel Test Micro Typing System

Leukemia & lymphoma, 1997, Vol.28 (1-2), p.177-182

1997

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Clinical improvement of β‐thal‐HbS anemia by iron deficiency

American journal of hematology, 1995-09, Vol.50 (1), p.68-69

1995

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Iron stores in multi-transfused thalassaemic patients seem not to be influenced by the HLA system

Haematologia, 2000-01, Vol.30 (4), p.319

2000

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Plesiomonas shigelloides Sepsis in a Thalassemia Intermedia Patient

Scandinavian journal of infectious diseases, 2002, Vol.34 (9), p.687-689

2002

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HIV infection due to a platelet transfusion after allogenic bone marrow transplantation

European journal of haematology, 1987, Vol.39 (2), p.185-189

1987

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Reduced incidence of GVHD in recipients of t-cell depleted marrow

Leukemia research, 1986, Vol.10 (1), p.122-122

1986

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HIV infection due to a platelet transfusion after allogeneic bone marrow transplantation

European Journal of Haematology, 1987, Vol.39 (2), p.185-189

1987

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Hemoglobinosis E in Greece

Sangre (Zaragoza), 1960, Vol.31, p.1

1960

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Bone marrow transplantation for patients with chronic myeloid leukaemia: T-cell depletion with Campath-1 reduces the incidence of graft-versus-host disease but may increase the risk of leukaemic relapse

Angioid Streaks in Sickle-Thalassemia

Hemothorax due to extramedullary erythropoietic masses

Transfusion‐induced hypoxemia in beta‐thalassaemia

Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report

Erythropoietin levels and microcytosis in heterozygous beta-thalassaemia

The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients

Development of plasma cell tumors during treatment of multiple myeloma

Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease

Chelation therapy in patients with thalassemia using the orally active iron chelator deferiprone (L1)

Evaluation of the clinical relevance of the expression and function of P-glycoprotein, multidrug resistance protein and lung resistance protein in patients with primary acute myelogenous leukemia

Spleen size in beta-thalassaemia heterozygotes

Randomized clinical trial comparing ceftriaxone/amikacin versus ceftazidime/amikacin as initial therapy of febrile episodes in neutropenic patients

Amelioration of Painful Crises in Sickle Cell Disease by Venesections

Immunological reconstitution after bone marrow transplant with Campath-1 treated bone marrow

HIV infection due to a platelet transfusion after allogeneic bone marrow transplantation

Multiple myeloma in sickle cell syndromes

Detection of "PNH Red Cell" Populations in Hematological Disorders Using the Sephacryl Gel Test Micro Typing System

Clinical improvement of β‐thal‐HbS anemia by iron deficiency

Iron stores in multi-transfused thalassaemic patients seem not to be influenced by the HLA system

Plesiomonas shigelloides Sepsis in a Thalassemia Intermedia Patient

HIV infection due to a platelet transfusion after allogenic bone marrow transplantation

Reduced incidence of GVHD in recipients of t-cell depleted marrow

HIV infection due to a platelet transfusion after allogeneic bone marrow transplantation

Hemoglobinosis E in Greece

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