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Curriculum Vitae

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Athanasios Evangeliou

Professor, School of Medicine

Personal Information

aeevange@auth.gr

Course Work

Courses of Winter semester of 2016–17 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics

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

Courses of Spring semester of 2016–17 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics
ΙΑ0325	Paediatrics I

Theses Supervised

Student Theses within AUTh

2011–2012

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

In progress

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

Research Projects

2016–2016	Έρευνα και θεραπεία οζώδους σκλήρυνσης και νεοεκφυλιστικών νοσημάτων και νευρογενετικών νοσημάτων
2013–2014	Νεώτερα στη νόσο του Pompe και λυσωσωμιακών
2011–2011	Νοσος του Niemann Pick Type C: Το μονοπατι της διάγνωσης

Publications

2015

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

Spilitoti Martha, Evangeliou Athanasios, Tramma Despoina, Theodoridou Zoi, Metaxas-Armodoros Spyridon, Michailidi E, Bonti Eleni, Frysira E, Haidopoulou Katerina, Asprangathou Despoina, Tsalkidis A, 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.

2011

Karagianni P, Tsakalidis C, Kyriakidou M, Mitsiakos G, Chatziioanidis H, Porpodi M, Evangeliou A, Nikolaides N (2011). Neuromotor outcomes in infants with bronchopulmonary dysplasia. Pediatr Neurol. vol.44 no.1 p.40-46.

2010

Evangeliou A, Gourgiotis D, Karagianni C, Markouri M, Anogianaki N, Mamoulakis D, Maropoulos G, Tsakalidis C, Frentzayias A, Nicolaidou P (2010). Carnitine status and lactate increase in patients with type I juvenile diabetes. Minerva Pediatr. vol.62 no.6 p.551-557.
Evangeliou Athanasios, Doulioglou V, Haidopoulou Katerina, Aptouramani M, 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. J Child Neurol. vol.25 no.12 p.1525-1528.
Karagianni P, Kyriakidou M, Mitsiakos G, Chatzioanidis H, Koumbaras E, Evangeliou A, Nikolaides N (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. J Child Neurol. 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 M, Evangeliou A, Stiakaki E, Giahnakis E, Kalmanti M (2010). Serum carnitine levels in childhood leukemia. J Pediatr Hematol Oncol. vol.32 no.2 p.e61-9.

2009

Evangeliou A, Vasilaki K, Karagianni P, Nikolaidis N (2009). Clinical applications of creatine supplementation on paediatrics. Curr Pharm Biotechnol. vol.10 no.7 p.683-690.
Evangeliou A, Spilioti M, Doulioglou V, Kalaidopoulou P, Ilias A, Skarpalezou A, Katsanika I, Kalamitsou S, Vasilaki K, Chatziioanidis I, Garganis K, et al (2009). Branched chain amino acids as adjunctive therapy to ketogenic diet in epilepsy: pilot study and hypothesis. J Child Neurol. vol.24 no.10 p.1268-1272.
Lefeber D. J, Schönberger J, Morava E, Guillard M, Huyben K. M, Verrijp K, Grafakou O, Evangeliou A, 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. Am J Hum Genet. vol.85 no.1 p.76-86.
Mantadakis E, Tsalkidis A, Paraskakis E, Papadopoulou-Legbelou K, Varlamis G, Evangeliou A, Chatzimichael A (2009). Anticonvulsant hypersensitivity syndrome closely mimicking Kawasaki disease. BMJ Case Rep. vol.2009.

2008

Contopoulos-Ioannidis D, Evangeliou A, terL.H, deV.B, Pfundt R, Scheffer H, Smeitink J, Tzoufi M, Makis A, Marinos E, Hess R, et al (2008). Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency. Am J Med Genet A. vol.146A no.23 p.3100-3103.
Raissaki M, Spilioti M, Kalaidopoulou P, Iliaki O, Mavrokosta M, Nikolaidis N, Evangeliou A (2008). Strabismus and nystagmus in a 4-year-old boy. Pediatr Ann. vol.37 no.9 p.590-593.
Sakellaris G, Nasis G, Kotsiou M, Tamiolaki M, Charissis G, Evangeliou A (2008). Prevention of traumatic headache, dizziness and fatigue with creatine administration. A pilot study. Acta Paediatr. vol.97 no.1 p.31-34.

2007

Evangeliou A, Papadopoulou-Legbelou K, Daphnis E, Ganotakis E, Vavouranakis I, Michailidou H, Hitoglou-Makedou A, Nicolaidou P, Wevers R, Varlamis G (2007). Cardiac manifestations of inborn errors of metabolism. Minerva Pediatr. vol.59 no.3 p.215-218.

2012

Spilitoti Martha, Tramma Despoina, Michailidi E, Spanou Sofia, Frysira E, Haidopoulou Katerina, Metaxas-Armodoros Spyridon, Asprangathou Despoina, Bonti Eleni, Tsalkidis A, 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 (Suppl 1):S1 – S182.

Aggiornato: 2017-08-06