Search Results - "Serbis, Anastasios"

The Molecular Basis of Neonatal Diabetes Mellitus and Transient Hyperglycemia in the Neonate.

Authors: Dermitzaki, Niki Serbis, Anastasios Baltogianni, Maria et al.

Source: Applied Sciences (2076-3417); Mar2026, Vol. 16 Issue 6, p2649, 22p

Molecular Genetics of Primary Congenital Hypothyroidism: Established and Emerging Contributors to Thyroid Dysgenesis.

Authors: Dermitzaki, Niki Serbis, Anastasios Baltogianni, Maria et al.

Source: International Journal of Molecular Sciences. Nov2025, Vol. 26 Issue 22, p10849. 19p.

Decoding Mini-Puberty and Its Clinical Significance: A Narrative Review.

Authors: Serbis, Anastasios Kosmeri, Chrysoula Atzemoglou, Natalia et al.

Source: Endocrines. Jun2025, Vol. 6 Issue 2, p28. 14p.

Permanent or Transient Congenital Hypothyroidism: A Diagnostic Dilemma.

Authors: Dermitzaki, Niki Serbis, Anastasios Baltogianni, Maria et al.

Source: Acta Paediatrica. Jan2026, Vol. 115 Issue 1, p43-54. 12p.

Predictive Factors for Pediatric Craniopharyngioma Recurrence: An Extensive Narrative Review.

Authors: Serbis, Anastasios Tsinopoulou, Vasiliki Rengina Papadopoulou, Anastasia et al.

Source: Diagnostics (2075-4418). May2023, Vol. 13 Issue 9, p1588. 20p.

Monogenic Defects of Beta Cell Function: From Clinical Suspicion to Genetic Diagnosis and Management of Rare Types of Diabetes.

Authors: Serbis, Anastasios Kantza, Evanthia Siomou, Ekaterini et al.

Source: International Journal of Molecular Sciences. Oct2024, Vol. 25 Issue 19, p10501. 18p.

Reply to commentary on "Predictive factors of permanent versus transient congenital hypothyroidism: a pragmatic cohort study".

Authors: Dermitzaki, Niki Giapros, Vasileios Deligeorgopoulou, Marianna et al.

Source: Annals of Pediatric Endocrinology & Metabolism. Aug2025, Vol. 30 Issue 4, p225-226. 2p.

Wolfram Syndrome 1: A Pediatrician's and Pediatric Endocrinologist's Perspective.

Authors: Serbis, Anastasios Rallis, Dimitrios Giapros, Vasileios et al.

Source: International Journal of Molecular Sciences. Feb2023, Vol. 24 Issue 4, p3690. 14p.

Which Diabetes Patients Will Benefit the Most from Once-Weekly Basal Insulin Analogs? A Review with a Special Focus on Type 1 Diabetes Patients.

Authors: Kosmeri, Chrysoula Baltogianni, Maria Giapros, Vasileios et al.

Source: Endocrines. Jun2024, Vol. 5 Issue 2, p214-224. 11p.

Predictive factors of permanent versus transient congenital hypothyroidism: a pragmatic cohort study.

Authors: Dermitzaki, Niki Giapros, Vasileios Deligeorgopoulou, Marianna et al.

Source: Annals of Pediatric Endocrinology & Metabolism. Jun2025, Vol. 30 Issue 3, p149-156. 8p.

Application of Advanced Molecular Methods to Study Early-Onset Neonatal Sepsis.

Authors: Kosmeri, Chrysoula Giapros, Vasileios Serbis, Anastasios et al.

Source: International Journal of Molecular Sciences. Feb2024, Vol. 25 Issue 4, p2258. 12p.

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin.

Authors: Tsinopoulou, Assimina Galli Serbis, Anastasios Kotanidou, Eleni P. et al.

Source: Journal of Clinical Research in Pediatric Endocrinology. Mar2018, Vol. 10 Issue 1, p74-78. 5p.

Cellular Localization of Orexin 1 Receptor in Human Hypothalamus and Morphological Analysis of Neurons Expressing the Receptor.

Authors: Vraka, Konstantina Mytilinaios, Dimitrios Katsenos, Andreas P. et al.

Source: Biomolecules (2218-273X). Apr2023, Vol. 13 Issue 4, p592. 16p.

The Prognostic Significance of BRAF Gene Analysis in Children and Adolescents with Papillary Thyroid Carcinoma: A Systematic Review and Meta-Analysis.

Authors: Kotanidou, Eleni P Giza, Styliani Tsinopoulou, Vasiliki Rengina et al.

Source: Diagnostics (2075-4418). Mar2023, Vol. 13 Issue 6, p1187. 18p.

Masked severe stenosing ureteritis: a rare complication of Henoch-Schönlein purpura.

Authors: Siomou, Ekaterini Serbis, Anastasios Salakos, Christos et al.

Source: Pediatric Nephrology. May2008, Vol. 23 Issue 5, p821-825. 5p. 1 Color Photograph, 1 Black and White Photograph, 1 Chart.

aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome.

Authors: Siomou, Ekaterini Gkoutsias, Athanasios Serbis, Anastasios et al.

Source: Pediatric Nephrology. Mar2016, Vol. 31 Issue 3, p513-517. 5p. 1 Graph.

Methylation haplotypes of the insulin gene promoter in children and adolescents with type 1 diabetes: Can a dimensionality reduction approach predict the disease?

Authors: Kotanidou, Eleni P. Kosvyra, Alexandra Mouzaki, Konstantina et al.

Source: Experimental & Therapeutic Medicine. Oct2023, Vol. 26 Issue 4, pN.PAG-N.PAG. 1p.

Osteoprotegerin increases parallel to insulin resistance in obese adolescents.

Authors: Kotanidou, Eleni P. Kotanidis, Christos P. Giza, Styliani et al.

Source: Endocrine Research. Feb-May2019, Vol. 44 Issue 1/2, p9-15. 7p. 4 Charts.

Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes.

Authors: Mouzaki, Konstantina Kotanidou, Eleni P. Fragou, Aikaterini et al.

Source: Biomedical Reports. Oct2020, Vol. 13 Issue 4, pN.PAG-N.PAG. 1p.

Genetically confirmed coexistence of neurofibromatosis type 1 and Cherubism in a pediatric patient.

Authors: Sarantou, Sofia Marinakis, Nikolaos M. Traeger-Synodinos, Joanne et al.

Source: Molecular biology reports 1/28/2024; Vol. 51 (1).

Journal Info: Publisher: Springer Nature ISSN: 0301-4851