E. Premetis

发表

Evaluation of liver fibrosis in patients with thalassemia: the important role of hyaluronic acid.

I. Papassotiriou, M. Papastamataki, P. Delaporta, 2010, Blood cells, molecules & diseases.

The effect of red cell shape on the measurement of red cell volume. A proposed method for the comparative assessment of this effect among various haematology analysers.

Nikolaos Laoutaris, G. Paterakis, D. Loukopoulos, 2008, Clinical and laboratory haematology.

Quantification of liver iron overload by T2 quantitative magnetic resonance imaging in thalassemia: impact of chronic hepatitis C on measurements.

A. Gouliamos, L. Nakopoulou, O. Papakonstantinou, 1999, Journal of pediatric hematology/oncology.

Effect of inflammation induced by prolonged exercise on circulating erythroid progenitors and markers of erythropoiesis

I. Papassotiriou, A. Margeli, M. Tsironi, 2010, Clinical chemistry and laboratory medicine.

Osteoporosis and osteosclerosis in sickle cell/beta-thalassemia: the role of the RANKL/osteoprotegerin axis.

I. Papassotiriou, E. Terpos, E. Voskaridou, 2006, Haematologica.

Erythropoietin Levels in Children and Adolescents With Inflammatory Bowel Disease

I. Papassotiriou, E. Roma, A. Tsitsika, 2005, Journal of pediatric hematology/oncology.

Unusual phenotypic observations associated with a rare HbH disease genotype (‐ ‐Med/αTSaudiα): implications for clinical management

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2002 .

Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β‐thalassaemia

I. Papassotiriou, G. Vassilopoulos, M. Marden, 1995 .

Terpos Osteoporosis and osteosclerosis in sickle cell / β-thalassemia : the role of the RANKL / osteoprotegerin axis

Evangelos, I. Papassotiriou, E. Voskaridou, 2006 .

A case of successful management with splenectomy of intractable ascites due to congenital dyserythropoietic anemia type II-induced cirrhosis.

A. Antoniadis, N. Nikolaidis, O. Giouleme, 2006, World journal of gastroenterology.

Arterial elastorrhexis in β‐thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis

E. Premetis, C. Fragodimitri, F. Karabatsos, 2001, European journal of haematology.

Iron overload and urinary lysosomal enzyme levels in β-thalassaemia major

H. Michelakakis, E. Dimitriou, E. Premetis, 1997, European Journal of Pediatrics.

The Impact of Neocyte Transfusion in the Management of Thalassaemia

I. Papassotiriou, C. Kattamis, E. Premetis, 1996, Vox sanguinis.

Ineffective erythropoiesis underlies the clinical heterogeneity of congenital dyserythropoietic anemia type II (CDA II)

I. Papassotiriou, S. Haidas, E. Premetis, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

Age, beta thalassaemia trait, and iron-deficient anaemia significantly affect reticulocyte indices in pre-school children

G. Chouliaras, E. Premetis, A. Stamoulakatou, 2010, European Journal of Pediatrics.

Erythropoiesis: Hereditary Spherocytosis in Greece: Collective Data on a Large Number of Patients.

D. Loukopoulos, E. Premetis, A. Stamoulakatou, 1999, Hematology.

Iron overload and urinary lysosomal enzyme levels in beta-thalassaemia major.

H. Michelakakis, E. Dimitriou, E. Premetis, 1997, European journal of pediatrics.

Serum transferrin receptors: Distribution and diagnostic performance in pre-school children.

I. Papassotiriou, G. Chouliaras, E. Premetis, 2009, Blood cells, molecules & diseases.

Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE.

I. Papassotiriou, D. Contopoulos-Ioannidis, I. Asproudis, 2006, Blood cells, molecules & diseases.

Rare thalassemic syndrome caused by interaction of Hb Questembert (α1 codon 131, TCT>CCT, Ser>Pro) with an α-thalassemia-2 deletion: implications for diagnosis and management

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2004 .