Euthymia Vargìami

Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome

Euthymia Vargìami, Athina Ververi, Maria Kyriazi et al. · American Journal of Medical Genetics Part A · 2013 · 54 citations

Identification of feeding risk factors for impaired nutrition status in paediatric patients with cerebral palsy

Τhomai Karagiozoglou‐Lampoudi, Efstratia Daskalou, Euthymia Vargìami et al. · Acta Paediatrica · 2012 · 40 citations

3-Hydroxy-3-Methylglutaryl Coenzyme A Lyase Deficiency with Reversible White Matter Changes after Treatment

Dimitrios Zafeiriou, Euthymia Vargìami, Ertan Mayapetek et al. · Pediatric Neurology · 2007 · 38 citations

Natural Sciences, Molecular Biology, Biochemistry

Association between iron deficiency and febrile seizures

Valia Papageorgiou, Euthymia Vargìami, E. Kontopoulos et al. · European Journal of Paediatric Neurology · 2015 · 34 citations

Electrolyte Disorder, Neurological Disorder, Iron Metabolism +6

Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder

Christos Chinopoulos, Spyros Batzios, Lambertus P. van den Heuvel et al. · Molecular Genetics and Metabolism · 2018 · 34 citations · Full text

Neurodegenerative Diseases, Suclg2 Protein, Molecular Neuroscience +11