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Curriculum Vitae

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Athanasios Evangeliou

Professor, School of Medicine

Personal Information

aeevange@auth.gr
Scopus ID6601972696
PubMed IDEvangeliou+A

Course Work

Courses of Winter semester of 2018–19 academic year

	TMĪMA IATRIKĪS
IA0378	Neurophysiology of Sensory Organs
ΙΑ0323	Paediatrics

	PROGRAMMA METAPTYCΗIAKŌN SPOUDŌN "EREUNĪTIKĪ METHODOLOGIA STĪN IATRIKĪ KAI STIS EPISTĪMES YGEIAS"
ΙΜΓ063

Courses of Spring semester of 2018–19 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics
ΙΑ0325	Paediatrics I

Theses Supervised

Student Theses within AUTh

In progress

Kalamitsou Serafeia. Χορήγηση της κρεατίνης ως επικουρική θεραπεία στην κετογονική δίαιτα σε παιδιά και εφήβους με ανθεκτική επιληψία
Papadopoulou Maria.
Dragoumi Maria. Οι διακυμάνσεις των επιπέδων της μελατονίνης και της κοπεπτίνης, στον ορό σε νεογνά, σε βρέφη και παιδιά, κατά τη διάρκεια του χειρουργικού stress
Aspragkathou Despoina. Χορήγηση αμινοξέων διακλαδιζόμενης αλύσου σε παιδιά με διάχυτη αναπτυξιακή διαταραχή

2011–2012

Doulioglou Vai. Χορήγηση τωναμινοξέων διακλαδιζόμενης αλύσου ως επικουρική θεραπεία της κετογονικής δίαιτας σε παιδιά με ανθεκτική επιληψία
Varlamis Sotirios. Η σημασία του μεταβολισμού της γλυκόζης στην παθοφυσιολογία των φαρμακοανθεκτικών επιληψιών στην παιδική ηλικία

Research Projects

2017–2019	Κετογονική δίαιτα
2016–2018	Ομιλίες – Συμβουλευτικές υπηρεσίες πάνω σε θέματα παιδικής νευρολογίας και μεταβολισμού.
2016–2017	Έρευνα και θεραπεία οζώδους σκλήρυνσης και νεοεκφυλιστικών νοσημάτων και νευρογενετικών νοσημάτων
2013–2014	Νεώτερα στη νόσο του Pompe και λυσωσωμιακών
2012–2015	Ερευνητικές δραστηριότητες Δ' Παιδιατρικής Κλινικής Α.Π.Θ.
2011–2011	Νοσος του Niemann Pick Type C: Το μονοπατι της διάγνωσης

Publications

2017

Without Type

Papathemeli Despoina, Mataftsi Asimina, Patsatsi Aikaterini, Sotiriadis Dimitrios, Samouilidou Maria, Chondromatidou S, Evangeliou Athanasios (2017). Atypical Presentation of Sjögren-Larsson Syndrome. Case reports in Pediatrics. vol. 17.

2015

Without Type

Barthélémy Florian, Navarro Claire, Fayek Racha, Da Silva Nathalie, Roll Patrice, Sigaudy Sabine, Oshima Junko, Bonne Gisèle, Papadopoulou-Legmpelou Kyriaki, Evangeliou Athanasios, Spilioti Martha, et al (2015). Truncated prelamin A expression in HGPS-like patients: a transcriptional study. European Journal of Human Genetics. vol.23 no.8 p.1051-1061.

2013

Without Type

Spilitoti Martha, Evangeliou Athanasios, Tramma Despoina, Theodoridou Zoi, Metaxas-Armodoros Spyridon, Michailidi Eleni, Bonti Eleni, Frysira Helen, Haidopoulou Katerina, Asprangathou Despoina, Tsalkidis Aggelos, et al (2013). Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD). Frontiers in Human Neuroscience. no.7 p. 858.

2012

Without Type

Spilitoti Martha, Tramma Despoina, Michailidi E, Spanou Sofia, Frysira Helen, Haidopoulou Katerina, Metaxas-Armodoros Spyridon, Asprangathou Despoina, Bonti Eleni, Tsalkidis Aggelos, Kardaras Panagiotis, et al (2012). Inborn errors of metabolism (IEM) and associated metabolic disturbances detected in a cohort of greek patients with autism spectrum disorder (ASD). Journal of Inherited Metabolic Diseases. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism. Birmingham - UK. Vol. 35 S.1 p.1–182.

2011

Without Type

Karagianni Paraskevi, Tsakalidis Christos, Kyriakidou M, Mitsiakos Georgios, Chatziioanidis H, Porpodi M, Evangeliou Athanasios, Nikolaidis Nikolaos (2011). Neuromotor outcomes in infants with bronchopulmonary dysplasia. Pediatric Neurology. vol.44 no.1 p.40-46.

2010

Without Type

Evangeliou Athanasios, Gourgiotis D, Karagianni C, Markouri M, Anogianaki N, Mamoulakis D, Maropoulos G, Tsakalidis Christos, Frentzayias A, Nicolaidou P (2010). Carnitine status and lactate increase in patients with type I juvenile diabetes. Minerva pediatrica. vol.62 no.6 p.551-557.
Evangeliou Athanasios, Doulioglou Vai, Haidopoulou Katerina, Aptouramani Maria, Spiliotou Martha, Varlamis Georgios (2010). Ketogenic diet in a patient with Angelman syndrome. Pediatrics International. vol.52 no.5 p.831-834.
Galli-Tsinopoulou Assimoula, Kyrgios I, Giannopoulou E. Z, Gourgoulia S, Maggana I, Katechaki E, Chatzidimitriou Dimitrios, Evangeliou Athanasios (2010). Acquired toxoplasmosis accompanied by facial nerve palsy in an immunocompetent 5-year-old child. Journal of Child Neurology. vol.25 no.12 p.1525-1528.
Karagianni Paraskevi, Kyriakidou M, Mitsiakos Georgios, Chatzioanidis H, Koumbaras E, Evangeliou Athanasios, Nikolaidis Nikolaos (2010). Neurological outcome in preterm small for gestational age infants compared to appropriate for gestational age preterm at the age of 18 months: a prospective study. Journal of Child Neurology. vol.25 no.2 p.165-170.
Leen W. G, Klepper J, Verbeek M. M, Leferink M, Hofste T, vanE, Wevers R. A, Arthur T, Bahi-Buisson N, Ballhausen D, Bekhof J, et al (2010). Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. Brain. vol.133 no.Pt 3 p.655-670.
Rogalidou Maria, Evangeliou Athanasios, Stiakaki Eftichia, Giahnakis Emmanuel, Kalmanti Maria (2010). Serum carnitine levels in childhood leukemia. Journal of Pediatric Hematology/Oncology. vol.32 no.2 p.e61-9.

2009

Without Type

Evangeliou Athanasios, Vasilaki K, Karagianni Paraskevi, Nikolaidis Nikolaos (2009). Clinical applications of creatine supplementation on paediatrics. Current Pharmaceutical Biotechnology. vol.10 no.7 p.683-690.
Evangeliou Athanasios, Spiliotou Martha, Doulioglou Vai, Kalaidopoulou Panagiota, Ilias Anestis, Skarpalezou Astrinia, Katsanika Irini, Kalamitsou Serafia, Vasilaki Konstantina, Chatziioanidis Ilias, Garganis Kiriakos, et al (2009). Branched chain amino acids as adjunctive therapy to ketogenic diet in epilepsy: pilot study and hypothesis. Journal of Child Neurology. vol.24 no.10 p.1268-1272.
Lefeber D. J, Schönberger J, Morava E, Guillard M, Huyben K. M, Verrijp K, Grafakou O, Evangeliou Athanasios, Preijers F. W, Manta P, Yildiz J, et al (2009). Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. The American Journal of Human Genetics. vol.85 no.1 p.76-86.
Mantadakis E, Tsalkidis A, Paraskakis E, Papadopoulou-Legmpelou Kyriaki, Varlamis Georgios, Evangeliou Athanasios, Chatzimichael A (2009). Anticonvulsant hypersensitivity syndrome closely mimicking Kawasaki disease. BMJ Case Rep. vol.2009.

2008

Without Type

Contopoulos-Ioannidis Despina, Evangeliou Athanasios, ter Laak Henk, de Vries Bert, Pfundt Rolph, Scheffer Hans, Smeitink Jan, Tzoufi Meropi, Makis Alexandros, Marinos Evangelos, Hess Richard, et al (2008). Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency. American Journal of Medical Genetics A. vol.146A no.23 p.3100-3103.
Raissaki Maria, Spiliotou Martha, Kalaidopoulou Panagiota, Iliaki Olga, Mavrokosta Maria, Nikolaidis Nikolaos, Evangeliou Athanasios (2008). Strabismus and nystagmus in a 4-year-old boy. Pediatric Annals. vol.37 no.9 p.590-593.
Sakellaris Georgios, Nasis George, Kotsiou Maria, Tamiolaki Maria, Charissis Giorgios, Evangeliou Athanasios (2008). Prevention of traumatic headache, dizziness and fatigue with creatine administration. A pilot study. Acta Paediatrica. vol.97 no.1 p.31-34.

2007

Without Type

Evangeliou Athanasios, Papadopoulou-Legmpelou Kyriaki, Daphnis E, Ganotakis E, Vavouranakis I, Michailidou H, Chitoglou-Makedou Areti, Nicolaidou P, Wevers R, Varlamis Georgios (2007). Cardiac manifestations of inborn errors of metabolism. Minerva Pediatric. vol.59 no.3 p.215-218.

Aktualisiert: 2018-11-01