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Pediatric Pulmonology|October 14, 2004
Can chest X-ray predict pneumonia severity?Olga Grafakou, Maria Moustaki, Maria Tsolia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 28, 2016
Valproate effect on ketosis in children under ketogenic dietMartha Spilioti, Evangelos Pavlou, Maria Gogou, et al.
Pediatric Pulmonology|March 12, 2003
Mesenteric lymphadenopathy as a cause of abdominal pain in children with lobar or segmental pneumoniaMaria Moustaki, Petros M Zeis, Maria Katsikari, et al.
BMC Medical Genomics|March 26, 2024
A novel large intragenic DPYD deletion causing dihydropyrimidine dehydrogenase deficiency: a case reportAnna Malekkou, Marios Tomazou, Gavriella Mavrikiou, et al.
European Journal of Pediatrics|August 20, 2003
Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutationOlga Grafakou, Konrad Oexle, Lambert van den Heuvel, et al.
Molecular Genetics and Metabolism Reports|November 25, 2024
A case series of Cypriot patients with CblC defect: Clinical, biochemical and molecular characteristicsTheodoros Georgiou, Olga Grafakou, Anna Malekkou, et al.
Molecular Genetics and Metabolism Reports|August 21, 2023
<i>GAA</i> variants associated with reduced enzymatic activity but lack of Pompe-related symptoms, incidentally identified by exome sequencingAnna Malekkou, Athina Theodosiou, Angelos Alexandrou, et al.
Journal of Inherited Metabolic Disease|April 21, 2025
YME1L1 Dysfunction Associated With 3-Methylglutaconic AciduriaAnthi Demetriadou, Olga Grafakou, Theodoros Georgiou, et al.
Molecular Genetics and Metabolism Reports|May 2, 2024
Inherited metabolic disorders in CyprusTheodoros Georgiou, Petros P Petrou, Anna Malekkou, et al.
Epilepsy & Behavior Reports|September 27, 2021
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromesIoannis Zaganas, Pelagia Vorgia, Martha Spilioti, et al.
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