Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης [ Τίτλος] Τύπος Έτος Φίλτρα: Συντάκτης is Zafeiriou, Dimitrios [Clear All Filters]
Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly..
Pediatr Res. 82(2), 253-260.
(2017). Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension..
Case Rep Pediatr. 2018, 5957987.
(2018).
(2014). Bayley-III scales at 12 months of corrected age in preterm infants: Patterns of developmental performance and correlations to environmental and biological influences..
Res Dev Disabil. 45-46, 110-9.
(2015). Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population..
J Neurosci Rural Pract. 6(4), 545-8.
(2015). Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth..
Iran J Child Neurol. 9(2), 21-8.
(2015). Exome Sequencing and the Management of Neurometabolic Disorders..
N Engl J Med. 374(23), 2246-55.
(2016). Identification of feeding risk factors for impaired nutrition status in paediatric patients with cerebral palsy..
Acta Paediatr. 101(6), 649-54.
(2012). Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece..
Am J Med Genet A. 155A(1), 58-68.
(2011). Mortality After Pediatric Arterial Ischemic Stroke..
Pediatrics. 141(5),
(2018). Neurological outcome at 6 and 12 months corrected age in hospitalised late preterm infants -a prospective study..
Eur J Paediatr Neurol. 22(4), 602-609.
(2018). Neurophysiologic evaluation of infants with congenital hypothyroidism before and after treatment..
Acta Neurol Belg. 115(2), 129-36.
(2015). Pandemic influenza A (H1N1) 2009-associated hemolytic uremic syndrome..
Pediatr Nephrol. 26(1), 143-4.
(2011). Pediatric Optic Pathway Gliomas: A Report From Northern Greece..
J Pediatr Hematol Oncol. 45(8), 445-451.
(2023).
(2022). Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome..
Eur J Paediatr Neurol. 22(3), 419-426.
(2018). Sleep disorders and executive function in children and adolescents with chronic kidney disease..
Sleep Med. 55, 33-39.
(2019). The Spectrum of Niemann-Pick Type C Disease in Greece..
JIMD Rep. 36, 41-48.
(2017). Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype..
Hum Mutat. 31(3), E1241-50.
(2010). Stüve-Wiedemann syndrome in a neonate..
Pediatr Int. 57(2), 302-4.
(2015). Subclinical central nervous system involvement and thrombophilic status in young thalassemia intermedia patients of Greek origin..
Blood Coagul Fibrinolysis. 23(3), 195-202.
(2012). Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection..
Curr Issues Mol Biol. 44(7), 2811-2824.
(2022).