Δημοσιεύσεις

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

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Συντάκτης Τίτλος [ Τύπος(Desc)] Έτος
Φίλτρα: Συντάκτης is Kalinderi, Kallirhoe  [Clear All Filters]
Journal Article
Chatzikyriakidou, A., Aidinidou L., Giannopoulos A., Papadopoulou-Legbelou K., Kalinderi K., & Fidani L. (2015).  Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients.. Cardiol Young. 25(4), 681-3.
Kara, E., Xiromerisiou G., Spanaki C., Bozi M., Koutsis G., Panas M., et al. (2014).  Assessment of Parkinson's disease risk loci in Greece.. Neurobiol Aging. 35(2), 442.e9-442.e16.
Gkampeta, A., Fidani L., Clarimón J., Kalinderi K., Katopodi T., Zafeiriou D., et al. (2014).  Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.. Epilepsy Res. 108(10), 1734-9.
Karakasis, C., Kalinderi K., Katsarou Z., Fidani L., & Bostantjopoulou S. (2011).  Association of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism with Parkinson's disease in a Greek population.. J Clin Neurosci. 18(12), 1744-5.
Fidani, L., Kalinderi K., Bostantjopoulou S., Clarimón J., Goulas A., Katsarou Z., et al. (2006).  Association of the Tau haplotype with Parkinson's disease in the Greek population.. Mov Disord. 21(7), 1036-9.
Kalinderi, K., Bostantjopoulou S., Paisan-Ruiz C., Katsarou Z., Hardy J., & Fidani L. (2009).  Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.. Neurosci Lett. 452(2), 87-9.
Kalinderis, M., Papanikolaou A., Kalinderi K., Ioannidou E., Giannoulis C., Karagiannis V., et al. (2011).  Elevated serum levels of interleukin-6, interleukin-1β and human chorionic gonadotropin in pre-eclampsia.. Am J Reprod Immunol. 66(6), 468-75.
Kalinderi, K., Fidani L., & Bostantjopoulou S. (2009).  From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome.. Parkinsonism Relat Disord. 15(1), 2-5.
Kalinderi, K., Fidani L., Katsarou Z., Clarimón J., Bostantjopoulou S., & Kotsis A. (2011).  GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort.. Neurobiol Aging. 32(3), 546.e1-5.
Kalinderi, K., Bostantjopoulou S., Katsarou Z., Clarimón J., & Fidani L. (2012).  Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population.. Genet Test Mol Biomarkers. 16(8), 974-7.
Kalinderi, K., Bostantjopoulou S., Katsarou Z., Clarimón J., & Fidani L. (2012).  Lack of association of the PICALM rs3851179 polymorphism with Parkinson's disease in the Greek population.. Int J Neurosci. 122(10), 502-605.
Kalinderi, K., Fragakis N., Sotiriadou M., Oriol D-I., Katritsis D., Letsas K., et al. (2018).  PRRX1 Rs3903239 polymorphism and atrial fibrillation in a Greek population.. Hellenic J Cardiol.
Kalogiannidis, I., Kalinderi K., Kalinderis M., Miliaras D., Tarlatzis B., & Athanasiadis A. (2018).  Recurrent complete hydatidiform mole: where we are, is there a safe gestational horizon? Opinion and mini-review.. J Assist Reprod Genet. 35(6), 967-973.
Kalinderis, M., Papanikolaou A., Kalinderi K., Vyzantiadis T-A., Ioakimidou A., & Tarlatzis B. C. (2015).  Serum levels of leptin and IP-10 in preeclampsia compared to controls.. Arch Gynecol Obstet. 292(2), 343-7.
Kalinderi, K., Delkos D., Kalinderis M., Athanasiadis A., & Kalogiannidis I. (2018).  Urinary tract infection during pregnancy: current concepts on a common multifaceted problem.. J Obstet Gynaecol. 38(4), 448-453.

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