Πρωτεύουσες καρτέλες
Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.
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).
Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager..
Case Reports Immunol. 2020, 8846827.
(2020).
Familial Mediterranean fever and atherosclerosis in childhood and adolescence..
Rheumatol Int. 40(1), 1-8.
(2020).
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases..
Ann Rheum Dis. 78(10), 1405-1411.
(2019).
Juvenile Recurrent Parotitis: The Role of Sialendoscopy..
Int J Inflam. 2019, 7278907.
(2019).
The multiple faces of Langerhans cell histiocytosis in childhood: A gentle reminder..
Mol Clin Oncol. 8(3), 489-492.
(2018).
Intavenous immunoglobulin for the management of intractable epilepsy in a boy..
Hippokratia. 21(1), 55-57.
(2017).
Development of the autoinflammatory disease damage index (ADDI)..
Ann Rheum Dis. 76(5), 821-830.
(2017).
Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies..
J Immunol Res. 2017, 1514294.
(2017).
Clinical Applications of Intravenous Immunoglobulins in Child Neurology..
Curr Pharm Biotechnol. 18(8), 628-637.
(2017).
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).
Valproate effect on ketosis in children under ketogenic diet..
Eur J Paediatr Neurol. 20(4), 555-9.
(2016).
Altered Expression of TLR2 and TLR4 on Peripheral CD14+ Blood Monocytes in Children with Urinary Tract Infection..
Biomed Res Int. 2016, 6052891.
(2016).
Prevalence of selective immunoglobulin A deficiency in Greek children and adolescents with type 1 diabetes..
World J Pediatr. 12(4), 470-476.
(2016).
Apelin and G212A apelin receptor gene polymorphism in obese and diabese youth..
Pediatr Obes. 10(3), 213-9.
(2015).
Evaluation and management of juvenile recurrent parotitis in children from northern Greece..
Hippokratia. 19(4), 356-9.
(2015).
Clinical picture and treatment of 2212 patients with common variable immunodeficiency..
J Allergy Clin Immunol. 134(1), 116-26.
(2014).
Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review..
Ann Rheum Dis. 72(5), 678-85.
(2013).
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).
Cardiac complications and immunophenotypic profile of infectious mononucleosis syndrome in children..
Indian Pediatr. 49(3), 195-8.
(2012).