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Publications

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

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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., 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., 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., 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.
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.
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.

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