Πρωτεύουσες καρτέλες
Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.
Pediatric Optic Pathway Gliomas: A Report From Northern Greece..
J Pediatr Hematol Oncol. 45(8), 445-451.
(2023).
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).
Sleep disorders and executive function in children and adolescents with chronic kidney disease..
Sleep Med. 55, 33-39.
(2019).
Correspondence regarding the systematic review entitled 'Evidence-based treatment of multicystic dysplastic kidney: a systematic review'..
J Pediatr Urol. 15(3), 291-292.
(2019).
Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease..
Blood Cells Mol Dis. 68, 203-208.
(2018).
Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome..
Eur J Paediatr Neurol. 22(3), 419-426.
(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).
Mortality After Pediatric Arterial Ischemic Stroke..
Pediatrics. 141(5),
(2018).
Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension..
Case Rep Pediatr. 2018, 5957987.
(2018).
Stroke and Hypertension in Children and Adolescents..
J Child Neurol. 32(4), 408-417.
(2017).
The Spectrum of Niemann-Pick Type C Disease in Greece..
JIMD Rep. 36, 41-48.
(2017).
Investigation of the motor system in two siblings with Canavan's disease: a combined transcranial magnetic stimulation (TMS) - diffusion tensor imaging (DTI) study..
Metab Brain Dis. 32(2), 307-310.
(2017).
Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly..
Pediatr Res. 82(2), 253-260.
(2017).
Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature..
Urology. 97, 194-196.
(2016).
Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome..
Case Rep Genet. 2016, 3056053.
(2016).
Exome Sequencing and the Management of Neurometabolic Disorders..
N Engl J Med. 374(23), 2246-55.
(2016).
The brainstem in late preterm birth: Born small-for-gestational-age is the "tip of the iceberg"..
Clin Neurophysiol. 127(9), 3178-3179.
(2016).
Neuroradiological, neurophysiological and molecular findings in infantile Krabbe disease: two case reports..
Balkan J Med Genet. 19(1), 85-90.
(2016).
High-fidelity over the somatosensory cortex revisited: back to basics..
Clin Neurophysiol. 126(2), 223-4.
(2015).
Neurophysiologic evaluation of infants with congenital hypothyroidism before and after treatment..
Acta Neurol Belg. 115(2), 129-36.
(2015).
Paroxysmal tonic upward gaze of childhood "plus": an oculomotor channelopathy?.
Eur J Paediatr Neurol. 19(3), 278-9.
(2015).
Stüve-Wiedemann syndrome in a neonate..
Pediatr Int. 57(2), 302-4.
(2015).