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Curriculum Vitae

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Efthymia Vargiami

Associate Professor, School of Medicine

Personal Information

evargiam@auth.gr
Scopus IDs56653344300, 6506811588
PubMed IDVargiami+E
Επιστημονική Ειδίκευση:
- Υγεία
- Ιατρική
- Ιατρικές υπηρεσίες

Education

Προπτυχιακές Σπουδές

1992	Ιατρική Α.Π.Θ. Greece Παιδίατρος-Παιδονευρολόγος

Διδακτορικό Δίπλωμα

2006	PhD Ιατρική Α.Π.Θ. Greece Παιδιατρική-Παιδονευρολογία

Μετεκπαίδευση

Great Ormond Street Hospital-London

Course Work

Courses of Winter semester of 2018–19 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics

Courses of Spring semester of 2018–19 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics
ΙΑ0324	Paediatric Development and Social Paediatrics
ΙΑ0325	Paediatrics I

Theses Supervised

Student Theses within AUTh

In progress

Sidira Christina-Spyridoula.
Katseni Vasiliki.

Research Projects

2018–2018	Καρδιά-Μυς-Ήπαρ: συνδέονται σε μια κοινή κλινική οντότητα
2015–2015	Αποκρυπτογραφώντας την Οζώδη σκλήρυνση στην παιδική ηλικία: απο το συμπτώματα στη διάγνωση
2014–2015	Παρουσίαση και συζήτηση σχετικά με την πολυσακχαρίδωση τύπου 1 (MPS.1)
2013–2013	Διαγνωστικός αλγόριθμος της όψιμης έναρξης της νόσου POMPE. Είναι εφαρμόσιμος στην Ελλάδα?

Publications

2016

Without Type

Vargiami Efthymia, Printza Nikoleta, Papadimiditriou Eleni, Batzios Spyros, Kyriazi Maria, Papachristou Fotios, Zafeiriou Dimitrios (2016). Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature. Urology. vol.97 p.194-196.

2012

Without Type

Printza Nikoleta, Ververi A, Bandouraki M, Vargiami Efthymia, Gidaris D, Papachristou Fotios (2012). Life-threatening hyponatremia and acute renal failure due to iatrogenic neonatal bladder rupture. Urologia Internationalis. Vol.88 no.2.
Zafeiriou Dimitrios, Papachristou Fotios, Ververi Athina, Printza Nikoleta, Mavridou Irini, Vargiami Efthymia, Giza Styliani, Michelakakis Helen (2012). A case of galactosialidosis with renal failure and hippocampal sclerosis. Journal of Pediatric Neurology. vol.10 no.1 p.45-48.

2011

Without Type

Batzios SP, Zafeiriou Dimitrios, Vargiami Efthymia, Karakiulakis George, Papakonstantinou Eleni (2011). Differential expression of matrix metalloproteinases in the serum of patients with mucopolysaccharidoses. Journal of Inherited Metabolic Disease. vol.3 p.59-66.
Teflioudi E. P, Zafeiriou Dimitrios, Vargiami Efthymia, Kontopoulos Eleftherios, Tsikoulas Ioannis (2011). Somatosensory evoked potentials in children with bilateral spastic cerebral palsy. Pediatric Neurology. vol.44 no.3 p.177-182.
Zafeiriou Dimitrios, Pavlidou E. L, Vargiami Efthymia (2011). Diverse clinical and genetic aspects of craniofrontonasal syndrome. Pediatric Neurology. vol.44 no.2 p.83-87.

2010

Without Type

Vargiami Efthymia, Zafeiriou Dimitrios (2010). Eponym: the Lemierre syndrome. European Journal of Pediatrics. vol.169 no.4 p.411-414.
Vargiami Efthymia, Farmaki Evangelia, Tasiopoulou D, Zafeiriou Dimitrios, Badouraki M, Anastasiou Athanasios, Karkos Christos, Gompakis Nikolaos, Athanasiou-Metaxa Miranta (2010). A patient with Lemierre syndrome. European Journal of Pediatrics. vol. 169 p. 491 – 493.

2009

Without Type

Vardarinos A, Zafeiriou Dimitrios, Vargiami Efthymia, Pratsidou-Gertsi P, Kontopoulos Eleftherios, Kanakoudi-Tsakalidou Florentia, Kozeis N, Mavromatis Ioannis (2009). Parental reports of health-related quality of life in greek children with neurofibromatosis type 1. The Journal of pediatrics. vol.155 no.3 p.453; author reply 454.
Zafeiriou Dimitrios, Willemsen M. A, Verbeek M. M, Vargiami Efthymia, Ververi A, Wevers R (2009). Tyrosine hydroxylase deficiency with severe clinical course. Molecular Genetics and Metabolism. vol.97 no.1 p.18-20.
Zafeiriou Dimitrios, Ververi A, Vargiami Efthymia (2009). The serotonergic system: its role in pathogenesis and early developmental treatment of autism. Curr Neuropharmacol. vol.7 no.2 p.150-157.
Zafeiriou Dimitrios, Lehmann-Horn F, Vargiami Efthymia, Teflioudi E, Ververi A, Jurkat-Rott K (2009). Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation. European Journal of Paediatric Neurology. vol.13 no.2 p.191-193.

2008

Without Type

Vargiami Efthymia, Zafeiriou Dimitrios, Gompakis Nikolaos, Kirkham F. J, Athanasiou-Metaxa Miranta (2008). Hemolytic anemia presenting with idiopathic intracranial hypertension. Pediatric Neurology. vol.38 no.1 p.53-54.
Verbeek M. M, Willemsen M, Wevers R. A, Lagerwerf A. J, Abeling N, Blau N, Thöny B, Vargiami Efthymia, Zafeiriou Dimitrios (2008). Two Greek siblings with sepiapterin reductase deficiency. Molecular Genetics and Metabolism. vol.94 no.4 p.403-409.
Zafeiriou Dimitrios, Ververi A, Salomons G. S, Vargiami Efthymia, Haas D, Papadopoulou V, Kontopoulos Eleftherios, Jakobs C (2008). L-2-Hydroxyglutaric aciduria presenting with severe autistic features. Brain Development. vol.30 no.4 p.305-307.
Zafeiriou Dimitrios, Vargiami Efthymia, Papadopoulou-Legmpelou Kyriaki, Dimitriou E, Mavridou I, Santamaria R, Canals I, Michelakakis H (2008). Serial magnetic resonance imaging and neurophysiological studies in multiple sulphatase deficiency. Eur J Paediatr Neurol. vol.12 no.3 p.190-194.

2007

Without Type

Megalopoulos A, Vasiliadis Konstantinos, Siminas S, Givissis Panagiotis, Vargiami Efthymia, Zafeiriou Dimitrios, Botsios Dimitrios, Betsis Dimitrios (2007). Pseudoaneurysm of the popliteal artery complicated by peroneal mononeuropathy in a 4-year-old child: report of a case. Surgery Today. vol.37 no.9 p.798-801.
Megalopoulos Angelos, Vasiliadis Konstantinos, Siminas Sotirios, Givissis Panagiotis, Vargiami Efthymia, Zafeiriou Dimitrios, Botsios Dimitrios, Betsis Dimitrios (2007). Pseudoaneurysm of the popliteal artery complicated by peroneal mononeuropathy in a 4- year-old-child: report of a case. Surgery Today. Vol.37 no.9 p.798-801.
Zafeiriou Dimitrios, Ververi A, Vargiami Efthymia (2007). Childhood autism and associated comorbidities. Brain Development. vol.29 no.5 p.257-272.
Zafeiriou Dimitrios, Vargiami Efthymia, Mayapetek E, Avgoustidou-Savvopoulou Persefoni, Mitchell G. A (2007). 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment. Pediatric Neurology. vol.37 no.1 p.47-50.
Zafeiriou Dimitrios, Avgoustidou-Savvopoulou Persefoni, Haas D, Smet J, Triantafyllou P, Vargiami Efthymia, Tamiolaki M, Gompakis Nikolaos, vanC.R, Sewell A. C, Vianey-Saban C, et al (2007). Ethylmalonic encephalopathy: clinical and biochemical observations. Neuropediatrics. vol.38 no.2 p.78-82.

Mis à jour: 2018-10-06