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 Galli-Tsinopoulou, Assimina [Clear All Filters]
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).
(2020).
DNA methylation analysis within the IL2RA gene promoter in youth with autoimmune thyroid disease..
Eur J Clin Invest. 50(3), e13199.
(2020). Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes..
Biomed Rep. 13(4), 31.
(2020). Metabolic Syndrome in Children and Adolescents: Is There a Universally Accepted Definition? Does it Matter?.
Metab Syndr Relat Disord.
(2020). Permanent damage of the sciatic nerve in an 8-year-old girl with newly diagnosed type 1 diabetes..
Paediatr Int Child Health. 40(1), 69-71.
(2020). De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome..
Cytogenet Genome Res. 158(1), 32-37.
(2019). Decreased cortisol response to low-dose Synacthen test in pediatric patients with type 1 diabetes..
J Diabetes. 11(9), 773-774.
(2019). l-selenomethionine supplementation in children and adolescents with autoimmune thyroiditis: A randomized double-blind placebo-controlled clinical trial..
J Clin Pharm Ther. 44(1), 102-108.
(2019). OPG/RANK/RANKL signaling axis in patients with type I diabetes: Associations with parathormone and vitamin D.
Italian Journal of Pediatrics. 453833713766225100202014162242852624771201315327557932511108646804835812323519351(1Suppl 129105),
(2019). OPG/RANK/RANKL signaling axis in patients with type I diabetes: Associations with parathormone and vitamin D..
Ital J Pediatr. 45(1), 161.
(2019). 46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin..
J Clin Res Pediatr Endocrinol. 10(1), 74-78.
(2018). Growth, the Mediterranean diet and the buying power of adolescents in Greece..
J Pediatr Endocrinol Metab. 31(7), 773-780.
(2018). The Intervention of Parents in Supporting of Diabetes Type 1 in Adolescents..
Mater Sociomed. 30(2), 98-102.
(2018). The multiple faces of Langerhans cell histiocytosis in childhood: A gentle reminder..
Mol Clin Oncol. 8(3), 489-492.
(2018). A Novel Variant c.97C>T of the Growth Hormone Releasing Hormone Receptor Gene Causes Isolated Growth Hormone Deficiency Type Ib.
J Clin Res Pediatr Endocrinol. 10(3), 284-288.
(2018).
(2018). Seasonality of month of birth in children and adolescents with autoimmune thyroiditis: a continuing conundrum..
J Pediatr Endocrinol Metab. 31(10), 1123-1131.
(2018). Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita..
Ann Pediatr Endocrinol Metab. 23(3), 162-165.
(2018). Impaired glucose metabolism and bronchial hyperresponsiveness in obese prepubertal asthmatic children..
Pediatr Pulmonol. 52(2), 160-166.
(2017). Psychological Aspects of Androgen Insensitivity Syndrome: Two Cases Illustrating Therapeutical Challenges..
Case Rep Endocrinol. 2017, 8313162.
(2017). Malnutrition in Hospitalized Pediatric Patients: Assessment, Prevalence, and Association to Adverse Outcomes..
J Am Coll Nutr. 35(4), 372-80.
(2016). Prevalence of selective immunoglobulin A deficiency in Greek children and adolescents with type 1 diabetes..
World J Pediatr. 12(4), 470-476.
(2016). Secondary nocturnal enuresis related to central diabetes insipidus as an early manifestation of intracranial germinomatous germ cell tumors in a series of male youngsters..
Ann Endocrinol (Paris). 76(1), 67-70.
(2015). Supplementation with long chain polyunsaturated fatty acids (LCPUFA) to breastfeeding mothers for improving child growth and development..
Cochrane Database Syst Rev. CD007901.
(2015).