Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης [ Τίτλος] Τύπος Έτος Φίλτρα: Συντάκτης is Papadopoulou-Alataki, Efimia [Clear All Filters]
Altered Expression of TLR2 and TLR4 on Peripheral CD14+ Blood Monocytes in Children with Urinary Tract Infection..
Biomed Res Int. 2016, 6052891.
(2016). Cardiac complications and immunophenotypic profile of infectious mononucleosis syndrome in children..
Indian Pediatr. 49(3), 195-8.
(2012). Clinical and biochemical manifestations of syndrome X in obese children..
Eur J Pediatr. 163(10), 573-9.
(2004). Clinical Applications of Intravenous Immunoglobulins in Child Neurology..
Curr Pharm Biotechnol. 18(8), 628-637.
(2017). Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases..
Ann Rheum Dis. 78(10), 1405-1411.
(2019). Clinical picture and treatment of 2212 patients with common variable immunodeficiency..
J Allergy Clin Immunol. 134(1), 116-26.
(2014). Development of the autoinflammatory disease damage index (ADDI)..
Ann Rheum Dis. 76(5), 821-830.
(2017).
(2019).
Familial Mediterranean fever and atherosclerosis in childhood and adolescence..
Rheumatol Int. 40(1), 1-8.
(2020). Hereditary angioedema in Greek families caused by novel and recurrent mutations..
Hum Immunol. 70(11), 925-9.
(2009). Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager..
Case Reports Immunol. 2020, 8846827.
(2020). Juvenile Recurrent Parotitis: The Role of Sialendoscopy..
Int J Inflam. 2019, 7278907.
(2019). Molecular diagnosis and management of hereditary angioedema in a Greek family..
Int Arch Allergy Immunol. 147(2), 166-70.
(2008). The multiple faces of Langerhans cell histiocytosis in childhood: A gentle reminder..
Mol Clin Oncol. 8(3), 489-492.
(2018). Performance of Different Diagnostic Criteria for Familial Mediterranean Fever in Children with Periodic Fevers: Results from a Multicenter International Registry..
J Rheumatol. 43(1), 154-60.
(2016). Prevalence of selective immunoglobulin A deficiency in Greek children and adolescents with type 1 diabetes..
World J Pediatr. 12(4), 470-476.
(2016). Prevention of infection in children and adolescents with primary immunodeficiency disorders..
Asian Pac J Allergy Immunol. 30(4), 249-58.
(2012). Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies..
J Immunol Res. 2017, 1514294.
(2017). Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children..
Ann Rheum Dis. 73(4), 662-7.
(2014). The role of PTPN22 C1858T gene polymorphism in diabetes mellitus type 1: first evaluation in Greek children and adolescents..
Biomed Res Int. 2013, 721604.
(2013).
(2019). Spine pathology in a girl with upper limb pain: A co-incidence or a causal relationship?.
Sudan J Paediatr. 17(1), 57-60.
(2017). Succinic Semialdehyde Dehydrogenase Deficiency Presenting as Autism Spectrum Disorder..
Indian J Pediatr. 83(9), 1036-7.
(2016). Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection..
Curr Issues Mol Biol. 44(7), 2811-2824.
(2022). TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies..
J Clin Immunol. 31(4), 550-9.
(2011).