Euthymia Vargìami

Aristotle University of Thessaloniki — Greece

Medicine · Health Sciences

15h-index860citations44works0.02yr avg
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Research Topics

Neonatal and fetal brain pathology(6), Metabolism and Genetic Disorders(5), Lysosomal Storage Disorders Research(4), Neurofibromatosis and Schwannoma Cases(4), Epilepsy research and treatment(3)

Publications44 total

Two Novel Mutations in the PSAP Gene Causing a Metachromatic Leukodystrophy (MLD)-like Phenotype and a Review of the Literature
Neurology India·2025Open Access
Phenotype assessment in neurologically impaired paediatric patients: Impact of a nutrition intervention protocol
Clinical Nutrition·2021· 5 cited
Transient Severe Liver Injury: A Unique Presentation of COVID-19 Disease in a Pediatric Patient
The Pediatric Infectious Disease Journal·2021· 12 cited
Hemolytic Uremic Syndrome Due to Methylmalonic Acidemia and Homocystinuria in an Infant: A Case Report and Literature Review
Children·2021· 8 citedOpen Access
Primitive Reflexes
The Encyclopedia of Child and Adolescent Development·2020
Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder
Molecular Genetics and Metabolism·2018· 34 citedOpen Access
Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension
Case Reports in Pediatrics·2018· 2 citedOpen Access
Clinical Aspects of Pediatric Brain Tumors
Journal of Pediatric Neuroradiology·2016
Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature
Urology·2016· 12 cited
Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome
Case Reports in Genetics·2016· 7 citedOpen Access
Cerebral embolism secondary to atrial myxoma in a child
Journal of Pediatric Neurology·2015
Cranial nerve palsies as presenting feature of acute lymphoblastic leukemia
Journal of Pediatric Neurology·2015· 1 cited
Association between iron deficiency and febrile seizures
European Journal of Paediatric Neurology·2015· 34 cited
Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth.
PubMed·2015· 22 citedOpen Access
Growth hormone replacement therapy in Costello syndrome
Growth Hormone & IGF Research·2014· 7 cited
High-fidelity over the somatosensory cortex revisited: Back to basics
Clinical Neurophysiology·2014· 1 cited
Moyamoya syndrome and neurofibromatosis type 1
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics·2014· 30 citedOpen Access
Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome
Journal of Pediatric Endocrinology and Metabolism·2014· 6 cited
Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome
American Journal of Medical Genetics Part A·2013· 54 cited
Incontinentia Pigmenti: A Skin, Brain, and Eye Matter
The Journal of Pediatrics·2013· 2 cited
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Frequent Co-authors

Dimitrios Zafeiriou(43), Athina Ververi(7), Maria Kyriazi(6), Athanasia Anastasiou(5), N. Gombakis(5), Spyros Batzios(4), Spyridon Gerou(3), E. Kontopoulos(3), Marina Economou(3), Panagiota Triantafyllou(3), Nikoleta Printza(3), Georgia Gioula(2), H Al-Mutawa(2), Marios Kambouris(2), Τhomai Karagiozoglou‐Lampoudi(2), Efstratia Daskalou(2), Ron A. Wevers(2), Fenella J. Kirkham(2), Helen Michelakakis(2), Fotiοs Papachristou(2)