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Publications

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

Export 24 results:
Author Title [ Type(Desc)] Year
Filters: Author is Fidani, Liana  [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.
Goulas, A., Fidani L., Kotsis A., Mirtsou V., Petersen R. C., Tangalos E., et al. (2002).  An association study of a functional catalase gene polymorphism, -262C-->T, and patients with Alzheimer's disease.. Neurosci Lett. 330(2), 210-3.
Goulas, A., Kosmidou M., Hatzitolios A. I., Raikos N., Molyva D., Savopoulos C., et al. (2008).  An association study of sodium-lithium countertransport activity with glutathione S transferase (GST) T1 and GST M1 null polymorphisms in Greek dyslipidaemic patients and controls.. Clin Chem Lab Med. 46(3), 306-10.
Fidani, L., Goulas A., Crook R., Petersen R. C., Tangalos E., Kotsis A., et al. (2004).  An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease.. Neurosci Lett. 357(2), 152-4.
Fidani, L., Athanassiadou-Piperopoulou F., Goulas A., Chatzidakis K., Koliouskas D., & Kotsis A. (2004).  An association study of the tumor necrosis factor alpha C-850T polymorphism and childhood acute lymphoblastic leukemia in a population from northern Greece.. Leuk Res. 28(10), 1053-5.
Gkampeta, A., Fidani L., Zafeiriou D., & Pavlou E. (2015).  Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population.. J Neurosci Rural Pract. 6(4), 545-8.
Fidani, L., Hatzitolios A. I., Goulas A., Savopoulos C., Basayannis C., & Kotsis A. (2005).  Cholesteryl ester transfer protein TaqI B and lipoprotein lipase Ser447Ter gene polymorphisms are not associated with ischaemic stroke in Greek patients.. Neurosci Lett. 384(1-2), 102-5.
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.
Dimitriadou, M., Christoforidis A., Economou M., Tsatra I., Vlachaki E., Fidani L., et al. (2010).  Elevated serum parathormone levels are associated with myocardial iron overload in patients with beta-thalassaemia major.. Eur J Haematol. 84(1), 64-71.
Dimitriadou, M., Christoforidis A., Fidani L., Economou M., Perifanis V., Tsatra I., et al. (2011).  Fok-I gene polymorphism of vitamin D receptor in patients with beta-thalassemia major and its effect on vitamin D status.. Hematology. 16(1), 54-8.
Dimitriadou, M., Christoforidis A., Economou M., Teli A., Printza N., Tzimouli V., et al. (2011).  Fok-I polymorphism of vitamin D receptor gene and the presence of renal dysfunction in patients with β-thalassemia major.. Pediatr Hematol Oncol. 28(6), 509-16.
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.
Goulas, A., Kosmidou M., Hatzitolios A. I., Molyva D., Fidani L., Giannopoulos S., et al. (2008).  Glutathione S-transferase null and cholesteryl ester transfer protein TaqI B polymorphisms and lipid response to atorvastatin in Greek dyslipidaemic patients.. Basic Clin Pharmacol Toxicol. 102(6), 559-62.
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.
Fidani, L., Goulas A., Mirtsou V., Petersen R. C., Tangalos E., Crook R., et al. (2002).  Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease.. Neurosci Lett. 323(1), 81-3.
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.
Chatzidakis, K., Goulas A., Athanassiadou-Piperopoulou F., Fidani L., Koliouskas D., & Mirtsou V. (2006).  Methylenetetrahydrofolate reductase C677T polymorphism: association with risk for childhood acute lymphoblastic leukemia and response during the initial phase of chemotherapy in greek patients.. Pediatr Blood Cancer. 47(2), 147-51.
Fidani, L., Compton D., Hardy J., Petersen R. C., Tangalos E., Mirtsou V., et al. (2002).  No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease.. Neurosci Lett. 322(3), 192-4.
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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