The molecular Basis of Thalassemia Syndromes

Haema 2011; 2(3): 225-234

by Joanne Traeger-Synodinos1, Christina Vrettou1,2, Manousos Papadakis3, Emmanuel Kanavakis1,2

1Laboratory of Medical Genetics, University of Athens, Choremeio Research Laboratory,
2Research Institute for the Study of Genetic and Malignant Disorders in Childhood, Aghia Sophia’s Children’s Hospital, Athens,
3Laboratory for Prenatal Diagnosis, Laiko Hospital, Athens, Greece

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Cytogenetic abnormalities in myelodysplastic syndromes: Clinical and prognostic impact

Haema 2011; 2(2): 177-186

by Charikleia Κelaidi1, Constantina Sabani2

1Department of Haematology and Bone Marrow Transplantation, G. Papanikolaou Hospital, Thessaloniki, Greece
2Laboratory of Health Physics & Environmental Health, National Center for Scientific Research “Demokritos”, Athens, Greece.

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Pathogenetic aspects of MDS: the role of apoptosis

Haema 2011; 2(2): 153-161

by Agapi Parcharidou1, Panagiota Tsoplou2, Αrgiris Symeonidis3

13rd Dept of Internal Medicine, Korgialeneio-Benakeio Hospital of Athens,
2BIOIATRIKI Laboratories, Dept of Human Genetics, Athens,
3Hematology Division, Dept of Internal Medicine, University of Patras Medical School, Patras.

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The role of monoclonal antibodies in the treatment of primary immune thrombocytopenia

Haema 2010; 1(2): 195-203

by Stavroula Masouridi MD and Photis Beris MD.

University Hematology Clinic, Laikon General Hospital, School of Medicine, National and Kapodistrian University of Athens – Greece.

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Novel thrombopoietic agents in the treatment of primary immune thrombocytopenia

Haema 2010; 1(2): 183-194

by Charalampos Pontikoglou

Heamatology Department, University of Crete School of Medicine, Heraklion, Greece, Establishment Français du Sang Centre-Atlantique, Research Dept, EA3855. GECSoM, Tours, France.

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