Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome..
Cytogenet Genome Res. 158(1), 32-37.
(2019). Psoriasis, arthritis, and pyoderma gangrenosum: an autoinflammatory syndrome or a coincidence?.
Int J Dermatol. 58(12), e240-e241.
(2019). Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly..
Pediatr Res. 82(2), 253-260.
(2017). Intranasal trigeminal function in patients with empty nose syndrome..
Laryngoscope. 127(6), 1263-1267.
(2017). [Cotard's syndrome: Case report and a brief review of literature]..
Psychiatriki. 27(4), 296-302.
(2016). Early-onset SMART Syndrome in an 11-Year-old Child With Acute Lymphoblastic Leukemia..
J Pediatr Hematol Oncol. 38(3), 248.
(2016). A systematic review and meta-analysis of glycemic control for the prevention of diabetic foot syndrome..
J Vasc Surg. 63(2 Suppl), 22S-28S.e1-2.
(2016). Tumor lysis-like syndrome in a child during treatment for visceral leishmaniasis..
Int J Immunopathol Pharmacol. 29(3), 458-60.
(2016). Clinically isolated syndrome manifested as acute vestibular syndrome: bedside neuro-otological examination and suppression of transient evoked otoacoustic emissions in the differential diagnosis..
Am J Otolaryngol. 35(5), 683-6.
(2014). Polythelia: simple atavistic remnant or a suspicious clinical sign for investigation?.
Pediatr Endocrinol Rev. 11(3), 290-7.
(2014). Popliteal artery entrapment syndrome: a common cause of a rare clinical entity--critical leg ischemia in the young..
Mil Med. 179(1), e124-6.
(2014). A 'posterior circulation stroke' that benefits from vitamins..
Am J Med. 127(2), e1-2.
(2014). Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014).
(2012).
(2012).
[Charles Bonnet syndrome: case reports and short review]..
Psychiatriki. 22(1), 68-72.
(2011). The stapled hemorrhoidopexy syndrome: a new clinical entity?.
Tech Coloproctol. 15 Suppl 1, S95-9.
(2011). Tardive Tourette-like syndrome: a systematic review..
Int Clin Psychopharmacol. 26(5), 237-42.
(2011). Eponym: the Lemierre syndrome..
Eur J Pediatr. 169(4), 411-4.
(2010). Giant villous adenoma and McKittrick-Wheelock syndrome in an incarcerated rectal prolapse..
Colorectal Dis. 12(4), 382-4.
(2010). Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder..
Brain. 133(Pt 3), 655-70.
(2010). Lady Windermere syndrome after cardiac surgery procedure: a case of Mycobacterium avium complex pneumonia..
Ann Thorac Surg. 89(4), 1296-9.
(2010). Lemierre syndrome: no delays in management..
Am J Emerg Med. 28(7), 844.e1-2.
(2010). A patient with Lemierre syndrome..
Eur J Pediatr. 169(4), 491-3.
(2010). Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype..
Hum Mutat. 31(3), E1241-50.
(2010).