Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 18 results:
Συντάκτης Τίτλος Τύπος [ Έτος] Φίλτρα: Συντάκτης is Economou, Marina [Clear All Filters]
Safety and Efficacy of Eltrombopag in Children and Adults with Immune Thrombocytopenia: a Systematic Review and Meta-analysis.:.
Cardiovascular & Hematological Agents in Medicinal Chemistry. 18,
(2020).
(2019).
(2018).
(2018).
Association between iron deficiency and febrile seizures..
Eur J Paediatr Neurol. 19(5), 591-6.
(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). Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene..
Pediatr Neurol. 50(6), 622-4.
(2014). Successful management of a small infant with Kasabach-Merritt phenomenon using vincristine: a case report..
Blood Coagul Fibrinolysis. 25(7), 777-9.
(2014). FcγRIIa and FcγRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome..
Blood Coagul Fibrinolysis. 24(1), 35-9.
(2013). Restrictive pulmonary dysfunction and its predictors in young patients with β-thalassaemia major..
Pediatr Pulmonol. 47(8), 801-7.
(2012). Subclinical central nervous system involvement and thrombophilic status in young thalassemia intermedia patients of Greek origin..
Blood Coagul Fibrinolysis. 23(3), 195-202.
(2012). Fok-I gene polymorphism of vitamin D receptor in patients with beta-thalassemia major and its effect on vitamin D status..
Hematology. 16(1), 54-8.
(2011). Fok-I polymorphism of vitamin D receptor gene and the presence of renal dysfunction in patients with β-thalassemia major..
Pediatr Hematol Oncol. 28(6), 509-16.
(2011). Elevated serum parathormone levels are associated with myocardial iron overload in patients with beta-thalassaemia major..
Eur J Haematol. 84(1), 64-71.
(2010). Haematuria in a young patient with severe haemophilia and inhibitor presence receiving prophylactic treatment with recombinant factor VIIa..
Blood Coagul Fibrinolysis. 21(6), 611-3.
(2010). Increased osteoclastic activity as shown by increased sRANK-L/OPG ratio in boys with hemophilia..
Ann Hematol. 89(8), 837-8.
(2010).
(2010). MRI assessment of liver iron content in thalassamic patients with three different protocols: comparisons and correlations..
Eur J Haematol. 82(5), 388-92.
(2009).