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Contribution of G71R mutation to Gilbert’s syndrome phenotype in a Greek patient:A case report

World journal of gastrointestinal pharmacology and therapeutics, 2011-10, Vol.2 (5), p.42-45

2011

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Polymorphisms of uridine glucuronosyltransferase gene and irinotecan toxicity: low dose does not protect from toxicity

Ecancermedicalscience, 2014-01, Vol.8, p.428

2014

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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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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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Analysis of the A(TA) nTAA 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, Vol.31 (1), p.38-42

2003

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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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Decreased expression of membrane α4β1, α5β1 integrins and transferrin receptor on erythroblasts in splenectomized patients with β-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Annals of hematology, 2003-09, Vol.82 (9), p.579-584

2003

Volltextzugriff (PDF)

Decreased expression of membrane alpha4beta1, alpha5beta1 integrins and transferrin receptor on erythroblasts in splenectomized patients with beta-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Annals of hematology, 2003-09, Vol.82 (9), p.579-584

2003

Volltextzugriff (PDF)

Amifostine protects normal pluripotent peripheral blood stem cells against the toxicity of idarubicin

Experimental hematology, 2000-07, Vol.28 (7), p.123

2000

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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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Decreased expression of membrane ?4?1, ?5?1 integrins and transferrin receptor on erythroblasts in splenectomized patients with ?-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Annals of hematology, 2003-09, Vol.82 (9), p.579-584

2003

Volltextzugriff (PDF)

Angioid Streaks in Sickle-Thalassemia

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

1994

Volltextzugriff (PDF)

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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Transfusion‐induced hypoxemia in beta‐thalassaemia

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

1996

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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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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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Contribution of G71R mutation to Gilbert’s syndrome phenotype in a Greek patient:A case report

Polymorphisms of uridine glucuronosyltransferase gene and irinotecan toxicity: low dose does not protect from toxicity

Hemothorax due to extramedullary erythropoietic masses

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

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

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)

Decreased expression of membrane α4β1, α5β1 integrins and transferrin receptor on erythroblasts in splenectomized patients with β-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Decreased expression of membrane alpha4beta1, alpha5beta1 integrins and transferrin receptor on erythroblasts in splenectomized patients with beta-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Amifostine protects normal pluripotent peripheral blood stem cells against the toxicity of idarubicin

Amelioration of Painful Crises in Sickle Cell Disease by Venesections

Decreased expression of membrane ?4?1, ?5?1 integrins and transferrin receptor on erythroblasts in splenectomized patients with ?-thalassemia intermedia. Parallel assessment of serum soluble transferrin receptors levels

Angioid Streaks in Sickle-Thalassemia

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

Transfusion‐induced hypoxemia in beta‐thalassaemia

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

Plesiomonas shigelloides Sepsis in a Thalassemia Intermedia Patient

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