Πρωτεύουσες καρτέλες
Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.
A Time Course of Bevacizumab (Anti-VEGF) Effect on Rat Peritoneum: Relations Between Antiadhesive Action and Fibrin Regulation Enzymes..
Surg Innov. 24(6), 543-551.
(2017).
Evaluation of the Greek TranQol: a novel questionnaire for measuring quality of life in transfusion-dependent thalassemia patients..
Ann Hematol. 96(11), 1937-1944.
(2017).
Hepatitis E in transfusion-dependent thalassaemia patients, in Greece: a single centre experience..
Vox Sang. 112(7), 678-679.
(2017).
evidence of complement activation in patients with sickle cell disease..
Haematologica. 102(12), e481-e482.
(2017).
Rivaroxaban Use in Patients with Hemoglobinopathies..
Hemoglobin. 41(3), 223-224.
(2017).
Association between response rates and survival outcomes in patients with newly diagnosed multiple myeloma. A systematic review and meta-regression analysis.
European Journal of Haematology. 98111125151171328622526459851317339343312102118301141312212432349259292117201512520158233100(6), 563 - 568.
(2017).
Evaluation of the Greek TranQol: a novel questionnaire for measuring quality of life in transfusion-dependent thalassemia patients.
Annals of Hematology. 9635386959511886953716410511460363056271262012394215457(1111435131343Suppl 21151168618233445), 1937 - 1944.
(2017).
Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease..
Hippokratia. 21(1), 43-45.
(2017).
Iron chelation therapy of transfusion-dependent β-thalassemia during pregnancy in the era of novel drugs: is deferasirox toxic?.
Int J Hematol. 103(5), 537-44.
(2016).
The Role of Angiogenesis in Haemophilic Arthropathy: Where Do We Stand and Where Are We Going?.
Turk J Haematol. 33(2), 88-93.
(2016).
A Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with Deferiprone..
Hemoglobin. 40(6), 435-437.
(2016).
A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major..
Osteoporos Int. 27(2), 781-8.
(2016).
Comment on "The correlation of Helicobacter pylori with the development of cholelithiasis and cholecystitis: the results of a prospective clinical study in Saudi Arabia"..
Eur Rev Med Pharmacol Sci. 20(1), 3-4.
(2016).
Accuracy of magnetic resonance imaging in diagnosis of liver iron overload: a systematic review and meta-analysis..
Clin Gastroenterol Hepatol. 13(1), 55-63.e5.
(2015).
Is there a role for low-dose eltrombopag as maintenance therapy in the treatment of immune thrombocytopenia?.
Acta Haematol. 133(1), 78-82.
(2015).
Evaluation of Mental Health and Physical Pain in Patients with β-Thalassemia Major in Northern Greece..
Hemoglobin. 39(3), 169-72.
(2015).
Diffuse gastric plasmacytoma involvement in multiple myeloma..
Endoscopy. 47 Suppl 1 UCTN, E197.
(2015).
Relationship between Helicobacter pylori infection and multiple sclerosis..
Ann Gastroenterol. 28(3), 353-356.
(2015).
Five Years of Deferasirox Therapy for Cardiac Iron in β-Thalassemia Major..
Hemoglobin. 39(5), 299-304.
(2015).
Combined chelation therapy with deferoxamine and deferiprone in β-thalassemia major: compliance and opinions of young thalassemic patients..
Hemoglobin. 38(2), 111-4.
(2014).
Successful Outcome of Chronic Intrahepatic Cholestasis in an Adult Patient with Sickle Cell/ β (+) Thalassemia..
Case Rep Hematol. 2014, 213631.
(2014).
Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene..
Pediatr Neurol. 50(6), 622-4.
(2014).
Primary gallbladder small lymphocytic lymphoma as a rare postcholecystectomy finding..
Case Rep Hematol. 2014, 716071.
(2014).
Thrombotic thrombocytopenic purpura or immune thrombocytopenia in a sickle cell/β+-thalassemia patient: a rare and challenging condition..
Transfus Apher Sci. 51(2), 175-7.
(2014).