Πρωτεύουσες καρτέλες
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Association between iron deficiency and febrile seizures..
Eur J Paediatr Neurol. 19(5), 591-6.
(2015).
Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth..
Iran J Child Neurol. 9(2), 21-8.
(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).
Growth hormone replacement therapy in Costello syndrome..
Growth Horm IGF Res. 24(6), 271-5.
(2014).
Update on transcobalamin deficiency: clinical presentation, treatment and outcome..
J Inherit Metab Dis. 37(3), 461-73.
(2014).
Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014).
Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene..
Pediatr Neurol. 50(6), 622-4.
(2014).
Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome..
J Pediatr Endocrinol Metab. 27(9-10), 967-70.
(2014).
Moyamoya syndrome and neurofibromatosis type 1..
Ital J Pediatr. 40, 59.
(2014).
Brain and spinal MR imaging findings in mucopolysaccharidoses: a review..
AJNR Am J Neuroradiol. 34(1), 5-13.
(2013).
Endothelial activation and inflammation biomarkers in children and adolescents with sickle cell disease..
Int J Hematol. 98(2), 158-63.
(2013).
Incontinentia pigmenti: a skin, brain, and eye matter..
J Pediatr. 163(5), 1520.
(2013).
Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long-term prognosis..
BMC Neurol. 13, 206.
(2013).
Unraveling the brainstem mysteries in late-preterm infants..
Clin Neurophysiol. 123(5), 852-3.
(2012).
Developing treatment options for metachromatic leukodystrophy..
Mol Genet Metab. 105(1), 56-63.
(2012).
Clinical and laboratory data in a sample of Greek children with autism spectrum disorders..
J Autism Dev Disord. 42(7), 1470-6.
(2012).
Subclinical central nervous system involvement and thrombophilic status in young thalassemia intermedia patients of Greek origin..
Blood Coagul Fibrinolysis. 23(3), 195-202.
(2012).
Identification of feeding risk factors for impaired nutrition status in paediatric patients with cerebral palsy..
Acta Paediatr. 101(6), 649-54.
(2012).
Noninvasive ultra high-frequency (1kHz) oscillations' recording: high-fidelity over somatosensory cortex..
Clin Neurophysiol. 123(12), 2323-4.
(2012).
Somatosensory evoked potentials in children with bilateral spastic cerebral palsy..
Pediatr Neurol. 44(3), 177-82.
(2011).
Pandemic influenza A (H1N1) 2009-associated hemolytic uremic syndrome..
Pediatr Nephrol. 26(1), 143-4.
(2011).
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).
Diverse clinical and genetic aspects of craniofrontonasal syndrome..
Pediatr Neurol. 44(2), 83-7.
(2011).