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).
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).
DNA hypermethylation of PTPN22 gene promoter in children and adolescents with Hashimoto thyroiditis..
J Endocrinol Invest.
(2020).
Diagnosis and management of Endocrine hypertension in children and adolescents..
Curr Pharm Des.
(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).
DNA methylation analysis within the IL2RA gene promoter in youth with autoimmune thyroid disease..
Eur J Clin Invest. 50(3), e13199.
(2020).
OPG/RANK/RANKL signaling axis in patients with type I diabetes: Associations with parathormone and vitamin D..
Ital J Pediatr. 45(1), 161.
(2019).
A novel FGF8 mutation in a female patient with isolated congenital anosmia..
Hormones (Athens). 18(2), 241-244.
(2019).
Decreased cortisol response to low-dose Synacthen test in pediatric patients with type 1 diabetes..
J Diabetes. 11(9), 773-774.
(2019).
De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome..
Cytogenet Genome Res. 158(1), 32-37.
(2019).
Could vitamin D deficiency influence left heart ventricular geometry in youngsters with type 1 diabetes mellitus?.
Hippokratia. 23(1), 9-14.
(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).
Unilateral renal agenesis as an early marker for genetic screening in Kallmann syndrome..
Hormones (Athens). 18(1), 103-105.
(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).
Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita..
Ann Pediatr Endocrinol Metab. 23(3), 162-165.
(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).
Seasonality of month of birth in children and adolescents with autoimmune thyroiditis: a continuing conundrum..
J Pediatr Endocrinol Metab. 31(10), 1123-1131.
(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).
Osteoprotegerin increases parallel to insulin resistance in obese adolescents..
Endocr Res. 1-7.
(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).
Exercise testing and adipokine levels for the evaluation of overweight and obesity in children..
Hippokratia. 21(3), 124-129.
(2017).
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