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 Vargiami, Euthymia [Clear All Filters]
Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension..
Case Rep Pediatr. 2018, 5957987.
(2018). 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). 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). Identification of feeding risk factors for impaired nutrition status in paediatric patients with cerebral palsy..
Acta Paediatr. 101(6), 649-54.
(2012). Incontinentia pigmenti: a skin, brain, and eye matter..
J Pediatr. 163(5), 1520.
(2013). Life-threatening hyponatremia and acute renal failure due to iatrogenic neonatal bladder rupture..
Urol Int. 88(2), 238-40.
(2012). 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). 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). Parental reports of health-related quality of life in greek children with neurofibromatosis type 1..
J Pediatr. 155(3), 453; author reply 454.
(2009). 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). Unraveling the brainstem mysteries in late-preterm infants..
Clin Neurophysiol. 123(5), 852-3.
(2012).