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Comparative study of dual energy X-ray absorptiometry and quantitative ultrasonography with the use of biochemical markers of bone turnover in boys with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-01, Vol.17 (1), p.e217-e222

2011

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Urine biochemical markers of early renal dysfunction are associated with iron overload in β-thalassaemia

Clinical and laboratory haematology, 2003-04, Vol.25 (2), p.105-109

2003

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Sequential therapy with activated prothrombin complex concentrate (FEIBA) and recombinant factor VIIa in a patient with severe haemophilia A, inhibitor presence and refractory bleeding

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-03, Vol.14 (2), p.390-391

2008

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The compatible MRI scoring system for staging of haemophilic arthropathy

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-07, Vol.14 (4), p.866-867

2008

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Avascular necrosis of the femoral head among children and adolescents with sickle cell disease in Greece

Haematologica (Roma), 2002-07, Vol.87 (7), p.771

2002

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A case of primary gastric lymphoma in a patient with thalassemia major

Leukemia & lymphoma, 2006-09, Vol.47 (9), p.1979-1981

2006

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A patient with Klinefelter's syndrome and thalassemia intermedia

Journal of Pediatric Endocrinology and Metabolism, 2005-04, Vol.18 (4), p.413

2005

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Yersinia enterocolitica mesenteric adenitis suspected by ultrasound examination

European journal of pediatrics, 1994-04, Vol.153 (4), p.299-299

1994

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Prevalence and severity of liver disease in patients with b thalassemia major. A single-institution fifteen-year experience

Haematologica (Roma), 2005-08, Vol.90 (8), p.1136-1138

2005

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Editor’s Highlights

European journal of obstetrics & gynecology and reproductive biology, 2002-03, Vol.101 (2), p.101-103

2002

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Long term audiological evaluation of beta-thalassemic patients

Acta oto-rhino-laryngologica Belgica, 2004, Vol.58 (2), p.113

2004

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Hearing loss in children with sickle cell disease

Acta oto-rhino-laryngologica Belgica, 2001, Vol.55 (3), p.235

2001

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Urine biochemical markers of early renal dysfunction are associated with iron overload in β-thalassaemia: Renal dysfunction markers in β-thalassaemia

Clinical and laboratory haematology, 2003-04, Vol.25 (2), p.105-109

2003

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Lithiase biliaire chez les patients drépanocytaires. Lˈexpérience grecque

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2002, Vol.9 (8), p.878-878

2002

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Effect of Cetirizine on Circulating Indicators of Persistent Inflammation and Endothelial Cell Activation in Patients With Sickle Cell Disease

Pediatric research, 1999-05, Vol.45, p.755-755

1999

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ELEVATED CIRCULATING INDICATORS OF PERSISTENT INFLAMMATION AND ENDOTHELIAL CELL ACTIVATION IN PATIENTS WITH SICKLE CELL DISEASE. 110

Pediatric research, 1997-05, Vol.41 (5), p.766-766

1997

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Biliary lithiasis in patients with sickle cell anemia. Greek experience

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2002-08, Vol.9 (8), p.878-878

2002

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Sequential therapy with activated prothrombin complex concentrate (FEIBA) and recombinant factor VIIa in a patient with severe haemophilia A, inhibitor presence and refractory bleeding

Haemophilia : the official journal of the World Federation of Hemophilia, 2008, Vol.14 (2), p.390-391

2008

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A case of primary gastric lymphoma in a patient with thalassemia major

Leukemia & lymphoma, 2006, Vol.47 (9), p.1979-1981

2006

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Yersinia enterocolitica mesenteric adenitis suspected by ultrasound examination

European journal of pediatrics, 1994, Vol.153 (4), p.299-299

1994

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Thirty-year experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimisation

European journal of haematology, 2013-04, Vol.90 (4), p.313-322

2013

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Renal Dysfunction in Patients with Beta-Thalassemia Major Receiving Iron Chelation Therapy either with Deferoxamine and Deferiprone or with Deferasirox

Acta haematologica, 2010-01, Vol.123 (3), p.148-152

2010

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Thirty‐year experience in preventing haemoglobinopathies in G reece: achievements and potentials for optimisation

European journal of haematology, 2013-04, Vol.90 (4), p.313-322

2013

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MRI assessment of liver iron content in thalassamic patients with three different protocols: comparisons and correlations

European journal of haematology, 2009-05, Vol.82 (5), p.388-392

2009

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Is liver stiffness really unrelated to liver iron concentration?

British journal of haematology, 2010-07, Vol.150 (2), p.247-248

2010

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Comparative study of dual energy X-ray absorptiometry and quantitative ultrasonography with the use of biochemical markers of bone turnover in boys with haemophilia

Urine biochemical markers of early renal dysfunction are associated with iron overload in β-thalassaemia

Sequential therapy with activated prothrombin complex concentrate (FEIBA) and recombinant factor VIIa in a patient with severe haemophilia A, inhibitor presence and refractory bleeding

The compatible MRI scoring system for staging of haemophilic arthropathy

Avascular necrosis of the femoral head among children and adolescents with sickle cell disease in Greece

A case of primary gastric lymphoma in a patient with thalassemia major

A patient with Klinefelter's syndrome and thalassemia intermedia

Yersinia enterocolitica mesenteric adenitis suspected by ultrasound examination

Prevalence and severity of liver disease in patients with b thalassemia major. A single-institution fifteen-year experience

Editor’s Highlights

Long term audiological evaluation of beta-thalassemic patients

Hearing loss in children with sickle cell disease

Urine biochemical markers of early renal dysfunction are associated with iron overload in β-thalassaemia: Renal dysfunction markers in β-thalassaemia

Lithiase biliaire chez les patients drépanocytaires. Lˈexpérience grecque

Effect of Cetirizine on Circulating Indicators of Persistent Inflammation and Endothelial Cell Activation in Patients With Sickle Cell Disease

ELEVATED CIRCULATING INDICATORS OF PERSISTENT INFLAMMATION AND ENDOTHELIAL CELL ACTIVATION IN PATIENTS WITH SICKLE CELL DISEASE. 110

Biliary lithiasis in patients with sickle cell anemia. Greek experience

Sequential therapy with activated prothrombin complex concentrate (FEIBA) and recombinant factor VIIa in a patient with severe haemophilia A, inhibitor presence and refractory bleeding

A case of primary gastric lymphoma in a patient with thalassemia major

Yersinia enterocolitica mesenteric adenitis suspected by ultrasound examination

Thirty-year experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimisation

Renal Dysfunction in Patients with Beta-Thalassemia Major Receiving Iron Chelation Therapy either with Deferoxamine and Deferiprone or with Deferasirox

Thirty‐year experience in preventing haemoglobinopathies in G reece: achievements and potentials for optimisation

MRI assessment of liver iron content in thalassamic patients with three different protocols: comparisons and correlations

Is liver stiffness really unrelated to liver iron concentration?

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