Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 20 results:
Συντάκτης [ Τίτλος] Τύπος Έτος Φίλτρα: Συντάκτης is Klonizakis, Philippos [Clear All Filters]
(2011).
Rivaroxaban Use in Patients with Hemoglobinopathies..
Hemoglobin. 41(3), 223-224.
(2017). Pure red cell aplasia and lymphoproliferative disorders: an infrequent association..
ScientificWorldJournal. 2012, 475313.
(2012). Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence..
Acta Haematol. 137(3), 175-182.
(2017). Pre- and Post-transfusion Complement Activation in Transfusion-dependent β-thalassaemia..
Hemasphere. 2(5), e58.
(2018). Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature..
Hemoglobin. 44(3), 221-223.
(2020).
(2012).
High prevalence of Helicobacter pylori infection in Greek patients with myelodysplastic syndromes..
Acta Haematol. 124(3), 141-9.
(2010). Helicobacter pylori's potential association with epilepsy..
Seizure. 21(2), 151.
(2012). Helicobacter pylori might be a potential therapeutic target in epilepsy..
Med Hypotheses. 76(5), 763.
(2011). Helicobacter pylori infection might contribute to esophageal adenocarcinoma progress in subpopulations with gastroesophageal reflux disease and Barrett's esophagus..
Helicobacter. 17(5), 402-3.
(2012). Helicobacter pylori infection may trigger Guillain-Barré syndrome, Fisher syndrome and Bickerstaff brainstem encephalitis..
J Neurol Sci. 305(1-2), 167-8; author reply 169.
(2011). Five Years of Deferasirox Therapy for Cardiac Iron in β-Thalassemia Major..
Hemoglobin. 39(5), 299-304.
(2015). Fatal refractory thrombotic thrombocytopenic purpura complicating systemic lupus erythematosus..
J Clin Rheumatol. 19(7), 412-4.
(2013).
(2009). evidence of complement activation in patients with sickle cell disease..
Haematologica. 102(12), e481-e482.
(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). 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).
(2018).
A Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with Deferiprone..
Hemoglobin. 40(6), 435-437.
(2016).