Search Results - "Litou, Eleni"

The Prognostic Significance of BRAF Gene Analysis in Children and Adolescents with Papillary Thyroid Carcinoma: A Systematic Review and Meta-Analysis by Kotanidou, Eleni P, Giza, Styliani, Tsinopoulou, Vasiliki Rengina, Margaritis, Kosmas, Papadopoulou, Anastasia, Sakellari, Eleni, Kolanis, Savvas, Litou, Eleni, Serbis, Anastasios, Galli-Tsinopoulou, Assimina

“…Thyroid cancer represents the prominent endocrine cancer in children. Papillary thyroid cancer (PTC) constitutes its most frequent (>90%) pediatric…”
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Predictive Factors for Pediatric Craniopharyngioma Recurrence: An Extensive Narrative Review by Serbis, Anastasios, Tsinopoulou, Vasiliki Rengina, Papadopoulou, Anastasia, Kolanis, Savvas, Sakellari, Eleni I, Margaritis, Kosmas, Litou, Eleni, Ntouma, Stergianna, Giza, Styliani, Kotanidou, Eleni P, Galli-Tsinopoulou, Assimina

“…Despite being classified as benign tumors, craniopharyngiomas (CPs) are associated with significant morbidity and mortality due to their location, growth…”
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46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin by Galli-Tsinopoulou, Assimina, Serbis, Anastasios, Kotanidou, Eleni P, Litou, Eleni, Dokousli, Vaia, Mouzaki, Konstantina, Fanis, Pavlos, Neocleous, Vassos, Skordis, Nicos

“…17-beta hydroxysteroid dehydrogenase type 3 (17βHSD-3) enzyme catalyzes the conversion of androstenedione (Δ4) to testosterone (T) in the testes of the…”
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Psychological Aspects of Androgen Insensitivity Syndrome: Two Cases Illustrating Therapeutical Challenges by Galli-Tsinopoulou, Assimina, Goulis, Dimitrios G., Mouzaki, Konstantina, Litou, Eleni, Kotanidou, Eleni P., Kyrgios, Ioannis, Kanakis, Georgios A., Pritsini, Filippa, Kleisarchaki, Aggeliki

“…Androgen Insensitivity Syndrome (AIS) and its heterogeneous phenotypes comprise the pieces of a challenging clinical problem. The lack of standardized…”
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Pseudohypoparathyroidism Type 1A with Normocalcaemia, due to the Novel C.389A>G Variant of Exon 5 of the Guanine Nucleotide-Binding Protein, α-Stimulating Gene by Kotanidou, Eleni P, Tsinopoulou, Vasiliki-Rengina, Serbis, Anastasios, Litou, Eleni, Galli-Tsinopoulou, Assimina

“…Pseudohypoparathyroidism type 1A (PHP1A) is a rare disease caused by molecular defects in the maternally-inherited allele of the guanine nucleotide-binding…”
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Permanent damage of the sciatic nerve in an 8-year-old girl with newly diagnosed type 1 diabetes by Giza, Styliani, Litou, Eleni, Kotanidou, Eleni P, Kleisarchaki, Angeliki N, Koliatos, Panagiotis, Tzirtzipis, Tasos, Tsinopoulou, Vasiliki Rengina, Tychalas, Athanasios, Evangeliou, Athanasios, Galli-Tsinopoulou, Assimina

“…Neuropathy, a complication of type 1 diabetes (T1D), is a heterogeneous group, and chronic polyneuropathy is the most common form in adults. Αn 8-year-old girl…”
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Permanent damage of the sciatic nerve in an 8-year-old girl with newly diagnosed type 1 diabetes by Giza, Styliani, Litou, Eleni, Kotanidou, Eleni P., Kleisarchaki, Angeliki N., Koliatos, Panagiotis, Tzirtzipis, Tasos, Tsinopoulou, Vasiliki Rengina, Tychalas, Athanasios, Evangeliou, Athanasios, Galli-Tsinopoulou, Assimina

“…Neuropathy, a complication of type 1 diabetes (T1D), is a heterogeneous group, and chronic polyneuropathy is the most common form in adults. Αn 8-year-old girl…”
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Psychological Aspects of Androgen Insensitivity Syndrome: Two Cases Illustrating Therapeutical Challenges by Pritsini, Filippa, Kanakis, Georgios A, Kyrgios, Ioannis, Kotanidou, Eleni P, Litou, Eleni, Mouzaki, Konstantina, Kleisarchaki, Aggeliki, Goulis, Dimitrios G, Galli-Tsinopoulou, Assimina

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