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 I [Clear All Filters]
Association between iron deficiency and febrile seizures..
Eur J Paediatr Neurol. 19(5), 591-6.
(2015). The brainstem in late preterm birth: Born small-for-gestational-age is the "tip of the iceberg"..
Clin Neurophysiol. 127(9), 3178-3179.
(2016). Childhood autism and auditory system abnormalities..
Pediatr Neurol. 42(5), 309-14.
(2010). Clinical and laboratory data in a sample of Greek children with autism spectrum disorders..
J Autism Dev Disord. 42(7), 1470-6.
(2012).
(2013).
(2015). Developing treatment options for metachromatic leukodystrophy..
Mol Genet Metab. 105(1), 56-63.
(2012). Diverse clinical and genetic aspects of craniofrontonasal syndrome..
Pediatr Neurol. 44(2), 83-7.
(2011). 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). Growth hormone replacement therapy in Costello syndrome..
Growth Horm IGF Res. 24(6), 271-5.
(2014). High-fidelity over the somatosensory cortex revisited: back to basics..
Clin Neurophysiol. 126(2), 223-4.
(2015). Incontinentia pigmenti: a skin, brain, and eye matter..
J Pediatr. 163(5), 1520.
(2013). L-2-Hydroxyglutaric aciduria: pattern of MR imaging abnormalities in 56 patients..
Radiology. 251(3), 856-65.
(2009). Moyamoya syndrome and neurofibromatosis type 1..
Ital J Pediatr. 40, 59.
(2014). Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome..
Case Rep Genet. 2016, 3056053.
(2016). Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene..
Pediatr Neurol. 50(6), 622-4.
(2014). Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature..
Urology. 97, 194-196.
(2016). Noninvasive ultra high-frequency (1kHz) oscillations' recording: high-fidelity over somatosensory cortex..
Clin Neurophysiol. 123(12), 2323-4.
(2012). An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study..
Hum Mutat. 31(4), 380-90.
(2010). Parental reports of health-related quality of life in greek children with neurofibromatosis type 1..
J Pediatr. 155(3), 453; author reply 454.
(2009). Paroxysmal tonic upward gaze of childhood "plus": an oculomotor channelopathy?.
Eur J Paediatr Neurol. 19(3), 278-9.
(2015). Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014). Somatosensory evoked potentials in children with bilateral spastic cerebral palsy..
Pediatr Neurol. 44(3), 177-82.
(2011). Stroke and Hypertension in Children and Adolescents..
J Child Neurol. 32(4), 408-417.
(2017). Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis..
Brain. 133(Pt 6), 1810-22.
(2010).