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: Keyword is Age of Onset [Clear All Filters]
APOE ε2 allele is associated with larger regional cortical thicknesses and volumes..
Dement Geriatr Cogn Disord. 30(3), 229-37.
(2010). Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas..
Clin Endocrinol (Oxf). 69(4), 621-7.
(2008). Association between solar insolation and a history of suicide attempts in bipolar I disorder..
J Psychiatr Res. 113, 1-9.
(2019). Central nervous system tumours among adolescents and young adults (15-39 years) in Southern and Eastern Europe: Registration improvements reveal higher incidence rates compared to the US..
Eur J Cancer. 86, 46-58.
(2017). Characteristics of psoriasis in Greece: an epidemiological study of a population in a sunny Mediterranean climate..
Eur J Dermatol. 20(2), 189-95.
(2010). Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases..
Ann Rheum Dis. 78(10), 1405-1411.
(2019). Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long-term prognosis..
BMC Neurol. 13, 206.
(2013). Clinical picture and treatment of 2212 patients with common variable immunodeficiency..
J Allergy Clin Immunol. 134(1), 116-26.
(2014). Comorbidity of obsessive-compulsive disorder with obsessive-compulsive personality disorder: Does it imply a specific subtype of obsessive-compulsive disorder?.
Psychiatry Res. 177(1-2), 156-60.
(2010). Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece..
Neurosci Lett. 452(2), 87-9.
(2009). Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease..
Acta Neuropathol. 134(3), 475-487.
(2017). Dissecting the damage in Northern Greek patients with childhood-onset systemic lupus erythematosus: a retrospective cohort study..
Rheumatol Int. 35(7), 1225-32.
(2015). Dupuytren in a Child: Rare Presentation of a Rare Clinical Entity..
J Hand Surg Am. 41(12), e477-e479.
(2016). Early onset degenerative dementias: demographic characteristics and etiologic classification in a tertiary referral center..
Acta Neurol Belg. 115(1), 27-31.
(2015). Familial aggregation of moderate to severe plaque psoriasis..
Clin Exp Dermatol. 39(7), 801-5.
(2014). Genetic assessment of familial and early-onset Parkinson's disease in a Greek population..
Eur J Neurol. 21(7), 963-8.
(2014). Genetic screening in adolescents with steroid-resistant nephrotic syndrome..
Kidney Int. 84(1), 206-13.
(2013). Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder..
Brain. 133(Pt 3), 655-70.
(2010). The Greek version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR)..
Rheumatol Int. 38(Suppl 1), 219-226.
(2018). Increased levels of proinflammatory cytokines in children with family history of coronary artery disease..
Clin Cardiol. 33(4), E6-10.
(2010). Influence of age, disease onset and ApoE4 on visual medial temporal lobe atrophy cut-offs..
J Intern Med. 275(3), 317-30.
(2014). Influence of birth cohort on age of onset cluster analysis in bipolar I disorder..
Eur Psychiatry. 30(1), 99-105.
(2015). Influence of light exposure during early life on the age of onset of bipolar disorder..
J Psychiatr Res. 64, 1-8.
(2015). Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations..
Neuromolecular Med. 19(1), 69-80.
(2017). Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease..
Neurosci Lett. 323(1), 81-3.
(2002).