Δημοσιεύσεις

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

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Συντάκτης Τίτλος [ Τύπος(Asc)] Έτος
Φίλτρα: Συντάκτης is Serbis, Anastasios  [Clear All Filters]
Journal Article
Serbis, A., Tsinopoulou V. Regina, Mouzaki K., Kotanidou E. P., Giza S., & Galli-Tsinopoulou A. (2018).  Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita.. Ann Pediatr Endocrinol Metab. 23(3), 162-165.
Kotanidou, E. P., Kotanidis C. P., Giza S., Serbis A., Tsinopoulou V-R., Karalazou P., et al. (2018).  Osteoprotegerin increases parallel to insulin resistance in obese adolescents.. Endocr Res. 1-7.
Kotanidou, E., Kosvyra A., Mouzaki K., Giza S., Tsinopoulou V., Serbis A., et al. (2023).  Methylation haplotypes of the insulin gene promoter in children and adolescents with type 1 diabetes: Can a dimensionality reduction approach predict the disease?. Experimental and Therapeutic Medicine. 26(4), 
Serbis, A., Giapros V., Galli-Tsinopoulou A., & Siomou E. (2020).  Metabolic Syndrome in Children and Adolescents: Is There a Universally Accepted Definition? Does it Matter?. Metab Syndr Relat Disord.
Mouzaki, K., Kotanidou E. P., Fragou A., Kyrgios I., Giza S., Kleisarchaki A., et al. (2020).  Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes.. Biomed Rep. 13(4), 31.
Mouzaki, K., Kotanidou E., Fragou A., Kyrgios I., Giza S., Kleisarchaki A., et al. (2020).  Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes. Biomedical Reports.
Serbis, A., Polyzos S. A., Paschou S. A., Siomou E., & Kiortsis D. N. (2024).  Diet, exercise, and supplements: what is their role in the management of the metabolic dysfunction-associated steatotic liver disease in children?. Endocrine.
Siomou, E., Gkoutsias A., Serbis A., Kollios K., Chaliasos N., & Frémeaux-Bacchi V. (2016).  aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome.. Pediatr Nephrol. 31(3), 513-7.
Galli-Tsinopoulou, A., Serbis A., Kotanidou E. P., Litou E., Dokousli V., Mouzaki K., et al. (2018).  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.

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Τμήμα Ιατρικής, Πανεπιστημιούπολη ΑΠΘ, T.K. 54124, Θεσσαλονίκη
 

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