Δημοσιεύσεις

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

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Φίλτρα: Keyword is Syndrome  [Clear All Filters]
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A
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.
C
Pagourelias, E. D., Koumaras C., Kakafika A. I., Tziomalos K., Zorou P. G., Athyros V. G., et al. (2009).  Cardiorenal anemia syndrome: do erythropoietin and iron therapy have a place in the treatment of heart failure?. Angiology. 60(1), 74-81.
Mitsiakos, G., Giougi E., Tsakalidis C., Kourti M., Chatziionnidis H., Karagianni P., et al. (2009).  A case of Adams-Oliver syndrome following in vitro fertilization.. Hum Reprod. 24(6), 1529-30.
Psarras, K., Ballas K. D., Pavlidis T. E., Rafailidis S., Symeonidis N., Marakis G. N., et al. (2009).  A case of Mirizzi's syndrome mimicking carcinoma: the role of CBD-stenting for easy surgical management.. J Laparoendosc Adv Surg Tech A. 19(4), 513-6.
Lagoudis, A., & Bozikas V. (2011).  [Charles Bonnet syndrome: case reports and short review].. Psychiatriki. 22(1), 68-72.
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.
Moschopoulos, N. P., Kaprinis S., & Nimatoudis J. (2016).  [Cotard's syndrome: Case report and a brief review of literature].. Psychiatriki. 27(4), 296-302.
D
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.
E
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.
Vargiami, E. G., & Zafeiriou D. I. (2010).  Eponym: the Lemierre syndrome.. Eur J Pediatr. 169(4), 411-4.
F
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.
Galli-Tsinopoulou, A., Emmanouilidou E., Karagianni P., Grigoriadou M., Kirkos J., & Varlamis G. S. (2008).  A female infant with Silver Russell Syndrome, mesocardia and enlargement of the clitoris.. Hormones (Athens). 7(1), 77-81.
G
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.
H
Prassopoulos, P. K., Raissaki M. T., & Gourtsoyiannis N. C. (1996).  Hepatodiaphragmatic interposition of the colon in the upright and supine position.. J Comput Assist Tomogr. 20(1), 151-3.
I
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.
L
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.
Karkos, P. D., Asrani S., Karkos C. D., Leong S. C., Theochari E. G., Alexopoulou T. D., et al. (2009).  Lemierre's syndrome: A systematic review.. Laryngoscope. 119(8), 1552-9.
Karkos, P. D., Karkanevatos A., Panagea S., Dingle A., & Davies J. E. (2004).  Lemierre's syndrome: how a sore throat can end in disaster.. Eur J Emerg Med. 11(4), 228-30.
Kouidou, S., Malousi A., & Maglaveras N. (2009).  Li-Fraumeni and Li-Fraumeni-like syndrome mutations in p53 are associated with exonic methylation and splicing regulatory elements.. Mol Carcinog. 48(10), 895-902.
M
Chatzopoulos, D., Iakovou I., & Moralidis E. (2007).  Marine-Lenhart syndrome and radioiodine-131 treatment.. Thyroid. 17(4), 373-4.
Tsalis, K. G., Zacharakis E., Kirou I. E., Sapidis N., Vagios I., Kalfadis S., et al. (2009).  Mirizzi syndrome with a fistula at the confluence of the hepatic ducts.. Med Sci Monit. 15(3), CS54-7.
N
Lazaridou, E., Apalla Z., Patsatsi A., Trigoni A., & Ioannides D. (2009).  Netherton's syndrome: successful treatment with isotretinoin.. J Eur Acad Dermatol Venereol. 23(2), 210-2.
P
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.

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