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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 38 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Syndrome  [Clear All Filters]
2019
Vittas, S., Efstathiou G., Tsakalidis C., Malamaki C., Antari V., Chatzitoliou E., et al. (2019).  De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome.. Cytogenet Genome Res. 158(1), 32-37.
Apalla, Z., Lallas A., Markakis K., Delli F., & Ioannides D. (2019).  Psoriasis, arthritis, and pyoderma gangrenosum: an autoinflammatory syndrome or a coincidence?. Int J Dermatol. 58(12), e240-e241.
2017
Tsoutsou, E., Tzetis M., Giannikou K., Braoudaki M., Mitrakos A., Amenta S., et al. (2017).  Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.. Pediatr Res. 82(2), 253-260.
Konstantinidis, I., Tsakiropoulou E., Chatziavramidis A., Ikonomidis C., & Markou K. (2017).  Intranasal trigeminal function in patients with empty nose syndrome.. Laryngoscope. 127(6), 1263-1267.
2016
Moschopoulos, N. P., Kaprinis S., & Nimatoudis J. (2016).  [Cotard's syndrome: Case report and a brief review of literature].. Psychiatriki. 27(4), 296-302.
Tsepis, K., Tragiannidis A., Gombakis N., & Hatzistilianou M. (2016).  Early-onset SMART Syndrome in an 11-Year-old Child With Acute Lymphoblastic Leukemia.. J Pediatr Hematol Oncol. 38(3), 248.
Hasan, R., Firwana B., Elraiyah T., Domecq J. Pablo, Prutsky G., Nabhan M., et al. (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.
Tragiannidis, A., Papageorgiou M., Stamou M., Hatzipantelis E., Papageorgiou T., Giannopoulos A., et al. (2016).  Tumor lysis-like syndrome in a child during treatment for visceral leishmaniasis.. Int J Immunopathol Pharmacol. 29(3), 458-60.
2014
Veros, K., Blioskas S., Karapanayiotides T., Psillas G., Markou K., & Tsaligopoulos M. (2014).  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.
Galli-Tsinopoulou, A., & Stergidou D. (2014).  Polythelia: simple atavistic remnant or a suspicious clinical sign for investigation?. Pediatr Endocrinol Rev. 11(3), 290-7.
Tsilogianni, Z., Grapatsas K., Papanikolaou Z., Kokkini-Paschou A., Tsantilas A., Tsiligiris V., et al. (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.
Karapanayiotides, T., Anastasiou A., Barmpas N., Grigoriadis N., & Karacostas D. (2014).  A 'posterior circulation stroke' that benefits from vitamins.. Am J Med. 127(2), e1-2.
Vargiami, E., Ververi A., Kyriazi M., Papathanasiou E., Gioula G., Gerou S., et al. (2014).  Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome.. Am J Med Genet A. 164A(3), 764-8.
2012
Kazakos, K., Kotsa K., Yavropoulou M., Dionyssopoulos A., Grabs R., Yovos J., et al. (2012).  Familial clustering strongly suggests that the phenotypic variation of the 8344 A>G lys mitochondrial tRNA mutation is encoded in cis.. Ann Hum Genet. 76(4), 296-300.
Vakalopoulos, I., Kampantais S., Dimopoulos P., Papastavros C., & Katsikas V. (2012).  Treatment of obstructive uropathy in one of three young brothers suffering from Gorlin-Cohen syndrome: a case report.. BMC Urol. 12, 2.
2011
Lagoudis, A., & Bozikas V. (2011).  [Charles Bonnet syndrome: case reports and short review].. Psychiatriki. 22(1), 68-72.
Efthimiadis, C., Kosmidis C., Grigoriou M., Anthimidis G., Vasiliadou K., Baka S., et al. (2011).  The stapled hemorrhoidopexy syndrome: a new clinical entity?. Tech Coloproctol. 15 Suppl 1, S95-9.
Fountoulakis, K. N., Samara M., Siapera M., & Iacovides A. (2011).  Tardive Tourette-like syndrome: a systematic review.. Int Clin Psychopharmacol. 26(5), 237-42.
2010
Vargiami, E. G., & Zafeiriou D. I. (2010).  Eponym: the Lemierre syndrome.. Eur J Pediatr. 169(4), 411-4.
Galanis, I. N., Dragoumis D. M., Christopoulos P. N., Galanis N. N., & Atmatzidis K. S. (2010).  Giant villous adenoma and McKittrick-Wheelock syndrome in an incarcerated rectal prolapse.. Colorectal Dis. 12(4), 382-4.
Leen, W. G., Klepper J., Verbeek M. M., Leferink M., Hofste T., van Engelen B. G., et al. (2010).  Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.. Brain. 133(Pt 3), 655-70.
Tryfon, S., Angelis N., Klein L., Tsirikos-Karapanos N., Karipidis E., Antoniadis A., et al. (2010).  Lady Windermere syndrome after cardiac surgery procedure: a case of Mycobacterium avium complex pneumonia.. Ann Thorac Surg. 89(4), 1296-9.
Karkos, P. D., Karkos C. D., Leong S. C., Sivaji N., Papadopoulos D., & Assimakopoulos A. D. (2010).  Lemierre syndrome: no delays in management.. Am J Emerg Med. 28(7), 844.e1-2.
Vargiami, E. G., Farmaki E., Tasiopoulou D., Zafeiriou D. I., Badouraki M., Anastasiou A., et al. (2010).  A patient with Lemierre syndrome.. Eur J Pediatr. 169(4), 491-3.
Perrault, I., Hanein S., Gerard X., Delphin N., Fares-Taie L., Gerber S., et al. (2010).  Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype.. Hum Mutat. 31(3), E1241-50.

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