Liana Fidani, MD PhD

Affiliations: 
Aristotle University of Thessaloniki, Thessaloniki, Greece 
Area:
http://www.biomedexperts.com/Profile.bme/398863/Liana_Fidani
Google:
"Liana Fidani"
Bio:

http://www.labome.org/expert/greece/aristotle/fidani/liana-fidani-588523.html

http://onlinelibrary.wiley.com/doi/10.1002/mds.20864/abstract

Mean distance: 19.3 (cluster 28)
 
Cross-listing: Alzheimer's Tree

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Publications

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Xiromerisiou G, Bourinaris T, Houlden H, et al. (2021) SORL1 mutation in a Greek family with Parkinson's disease and dementia. Annals of Clinical and Translational Neurology
Gogou M, Pavlou E, Kimiskidis V, et al. (2021) Novel Mutations Involved in Charcot-Marie-Tooth 4C and Intrafamilial Variability: Let's Not Miss the Forest for the Trees. Journal of Pediatric Genetics. 10: 147-151
Gogou M, Pavlou E, Kimiskidis V, et al. (2020) Novel Mutations Involved in Charcot-Marie-Tooth 4C and Intrafamilial Variability: Let's Not Miss the Forest for the Trees Journal of Pediatric Genetics
Kalinderi K, Papaliagkas V, Fidani L. (2018) Pharmacogenetics and levodopa induced motor complications. The International Journal of Neuroscience. 1-31
Kalinderi K, Fragakis N, Sotiriadou M, et al. (2018) PRRX1 Rs3903239 Polymorphism and Atrial Fibrillation in a Greek Population. Hellenic Journal of Cardiology : Hjc = Hellenike Kardiologike Epitheorese
Kalinderi K, Bostantjopoulou S, Fidani L. (2016) The genetic background of Parkinson's disease: Current progress and future prospects Acta Neurologica Scandinavica
Gkampeta A, Fidani L, Zafeiriou D, et al. (2015) Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population. Journal of Neurosciences in Rural Practice. 6: 545-548
Kalinderi K, Bostantjopoulou S, Katsarou Z, et al. (2015) D620N mutation in the VPS35 gene and R1205H mutation in the EIF4G1 gene are uncommon in the Greek population. Neuroscience Letters. 606: 113-6
Dimitriadou M, Christoforidis A, Fidani L, et al. (2015) A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa
Kalinderi K, Fragakis N, Koskinas KC, et al. (2015) Association Between rs2200733 Polymorphism on Chromosome 4q25 and Atrial Fibrillation in a Greek Population. Hellenic Journal of Cardiology : Hjc = HellēNikē Kardiologikē EpitheōRēSē. 56: 224-9
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