Efthimia Vargiami
Overview
Explore the profile of Efthimia Vargiami including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
5
Citations
16
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0
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Recent Articles
1.
Papadimas G, Vargiami E, Dragoumi P, Van Coster R, Smet J, Seneca S, et al.
Acta Myol
. 2020 Sep;
39(2):94-97.
PMID: 32904881
The mitochondrial DNA depletion syndrome (MDDS) is characterized by extensive phenotypic variability and is due to nuclear gene mutations resulting in reduced mtDNA copy number. Thymidine kinase 2 (TK2) mutations...
2.
Athanasiadou E, Vlachou C, Theocharidou A, Tilaveridis I, Vargiami E, Antoniadis K, et al.
Spec Care Dentist
. 2019 Nov;
40(1):113-120.
PMID: 31674703
Background/aim: Osteopetrosis is an inherited disease characterized by increased bone density. Its genetic variability results in various phenotype expressions, whereas clinically are classified in three types: malignant infantile, intermediate and...
3.
Economou M, Teli A, Gourtsa V, Vargiami E, Zafeiriou D
J Pediatr Hematol Oncol
. 2016 May;
38(5):406.
PMID: 27164520
No abstract available.
4.
Dragoumi P, Tzetzi O, Vargiami E, Pavlou E, Krikonis K, Kontopoulos E, et al.
BMC Neurol
. 2013 Dec;
13:206.
PMID: 24350775
Background: Idiopathic epilepsies and epileptic syndromes predominate childhood and adolescence epilepsy. The aim of the present study was to investigate the clinical course and outcome of idiopathic childhood epilepsy and...
5.
Megalopoulos A, Vasiliadis K, Siminas S, Givissis P, Vargiami E, Zafeiriou D, et al.
Surg Today
. 2007 Aug;
37(9):798-801.
PMID: 17713737
Pseudoaneurysms of the popliteal artery (PPA) rarely occur in children. In fact, we found only 10 cases reported in the medical literature. We report the case of a 4-year-old boy...