P1695: CEREBRAL VENOUS THROMBOSIS AND ANTITHROMBOTIC THERAPY: A SYSTEMATIC REVIEW by Papageorgiou, V., Lefkou, E., Xiromerisiou, G., Girtovitis, F., Matsagkas, M.

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Association between 9p21–23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and Diet by Mourtzi, N., Hatzimanolis, A., Xiromerisiou, G., Ntanasi, E., Georgakis, M. K., Ramirez, A., Heilmann-Heimbach, S., Grenier-Boley, B., Lambert, J. C., Yannakoulia, M., Kosmidis, M., Dardiotis, E., Hadjigeorgiou, G., Sakka, P., Scarmeas, Nikolaos

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Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson’s disease: analysis of a large multi-center study by Wang, L., MS, Heckman, M.G., MS, Aasly, J.O., MD, Annesi, G., PhD, Bozi, M., MD, Chung, S.J., MD, Clarke, C., MD, Crosiers, D., MD, Eckstein, G., PhD, Garraux, G., MD, Hadjigeorgiou, G.M., MD, Hattori, N., MD, PhD, Jeon, B., MD, Kim, Y.J., MD PhD, Kubo, M, Lesage, S., PhD, Lin, J.J., MD, Lynch, T., MD, Lichtner, P., PhD, Mellick, G.D., PhD, Mok, V., MD, Morrison, K.E., MD, Quattrone, A., MD, Satake, W., MD PhD, Silburn, P.A., MD, Stefanis, L., MD, Stockton, J.D., MD, Tan, E.K., MD, Toda, T., MD PhD, Brice, A., MD, Van Broeckhoven, C., PhD, Uitti, R.J., MD, Wirdefeldt, K., MD PhD, Wszolek, Z., MD, Xiromerisiou, G., MD, Maraganore, D.M., MD, Gasser, T., MD, Krüger, R., MD, Farrer, M.J., PhD, Ross, O.A., PhD, Sharma, M., PhD

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The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database by Marogianni, Chrysoula, Rikos, Dimitrios, Provatas, Antonios, Dadouli, Katerina, Ntellas, Panagiotis, Tsitsi, Panagiota, Patrinos, George, Dardiotis, Efthimios, Hadjigeorgiou, George, Xiromerisiou, Georgia

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Testing association between LRRK2 and Parkinson’s disease and investigating linkage disequilibrium by Paisán-Ruíz, C, Evans, E W, Jain, S, Xiromerisiou, G, Gibbs, J R, Eerola, J, Gourbali, V, Hellström, O, Duckworth, J, Papadimitriou, A, Tienari, P J, Hadjigeorgiou, G M, Singleton, A B

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation by Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zamba‐Papanicolaou, Eleni, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Kernohan, Kristin D., Eaton, Alison, Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Zetterberg, Henrik, Heales, Simon J. R., Rothman, James E., Clayton, Peter T., Houlden, Henry, Kriouile, Yamna, Aguennouz, Mhammed, Groppa, Stanislav, Marinova Karashova, Blagovesta, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez‐Dueñas, Belen, Di Rosa, Gabriella, Goraya, Jatinder S., Sultan, Tipu, Mine, Jun, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Pineda‐Marfa, Mercedes, Ferrari, Michel D., van den Maagdenberg, Arn M J M, Verrotti, Alberto, Marseglia, Giangluigi, García‐Silva, Mayte, Ruiz, Alfons Macaya, Garavaglia, Barbara, Borgione, Eugenia, Portaro, Simona, Boles, Richard, Giunti, Paola, Chelban, Viorica, Salpietro, Vincenzo, Efthymiou, Stephanie, Kullmann, Dimitri, Kaiyrzhanov, Rauan, Sullivan, Roisin, Khan, Alaa Matooq, Yau, Wai Yan, Papanicolaou, Eleni Zamba, Maqbool, Shazia, Rana, Nuzhat Noureen, Atawneh, Osama, Shaikh, Farooq, Koutsis, George, Breza, Marianthi, Mangano, Salvatore, Scuderi, Carmela, Borgione, Eugenia, Stojkovic, Tanya, Torti, Erin, Zollo, Massimi, Dauvilliers, Yves A., Rizig, Mie, Okubadejo, Njideka U., Ojo, Oluwadamilola O., Wahab, Kolawole, Bello, Abiodun H., Obiabo, Yahaya, Nwazor, Ernest, Iyagba, Alagoma, Taiwo, Lolade, Komolafe, Morenikeji, Oguntunde, Olapeju, Senkevich, Konstantin, Haridy, Nourelhoda, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Isrofilov, Maksud, Khachatryan, Samson, Silvestri, Gabriella, Bourinaris, Thomas, Fidani, Liana

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BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groups by Xiromerisiou, G., Hadjigeorgiou, G.M., Eerola, J., Fernandez, H.H., Tsimourtou, V., Mandel, R., Hellström, O., Gwinn-Hardy, K., Okun, M.S., Tienari, P.J., Singleton, A.B.

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Case report: CADASIL by Koutsouraki, E, Traka, M, Avdelidi, E, Xiromerisiou, G, Costa, V, Baloyannis, S

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Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene by Daiou, C., Christodoulou, K., Xiromerisiou, G., Panas, M., Dardiotis, E., Kladi, A., Speletas, M., Ntaios, G., Papadimitriou, A., Germenis, A., Hadjigeorgiou, Georgios M.

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Independent and joint effects of the MAPT and SNCA genes in Parkinson disease by Elbaz, Alexis, Ross, Owen A., Ioannidis, John P. A., Soto-Ortolaza, Alexandra I., Moisan, Frédéric, Aasly, Jan, Annesi, Grazia, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Gibson, J. Mark, Gispert, Suzana, Hadjigeorgiou, Georgios M., Jasinska-Myga, Barbara, Klein, Christine, Krüger, Rejko, Lambert, Jean-Charles, Lohmann, Katja, van de Loo, Simone, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugénie, Nilsson, Christer, Opala, Grzegorz, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Stefanis, Leonidas, Uitti, Ryan J., Valente, Enza Maria, Vilariño-Güell, Carles, Wirdefeldt, Karin, Wszolek, Zbigniew K., Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J.

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The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants by Heckman, Michael G, Elbaz, Alexis, Soto-Ortolaza, Alexandra I, Serie, Daniel J, Aasly, Jan O, Annesi, Grazia, Auburger, Georg, Bacon, Justin A, Boczarska-Jedynak, Magdalena, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Ioannidis, John P.A, Jasinska-Myga, Barbara, Jeon, Beom S, Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A, Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J, Valente, Enza Maria, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Wirdefeldt, Karin, Wszolek, Zbigniew K, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A

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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease by Krüger, Rejko, Sharma, Manu, Riess, Olaf, Gasser, Thomas, Van Broeckhoven, Christine, Theuns, Jessie, Aasly, Jan, Annesi, Grazia, Bentivoglio, Anna Rita, Brice, Alexis, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Ioannidis, John P.A, Jasinska-Myga, Barbara, Klein, Christine, Lambert, Jean-Charles, Lesage, Suzanne, Lin, Juei-Jueng, Lynch, Timothy, Mellick, George D, de Nigris, Francesa, Opala, Grzegorz, Prigione, Alessandro, Quattrone, Aldo, Ross, Owen A, Satake, Wataru, Silburn, Peter A, Tan, Eng King, Toda, Tatsushi, Tomiyama, Hiroyuki, Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Maraganore, Demetrius M

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Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study by Wang, Lisa, Heckman, Michael G., Aasly, Jan O., Annesi, Grazia, Bozi, Maria, Chung, Sun Ju, Clarke, Carl, Crosiers, David, Eckstein, Gertrud, Garraux, Gaetan, Hadjigeorgiou, Georgios M., Hattori, Nobu, Jeon, Beom, Kim, Yun J., Kubo, Masato, Lesage, Suzanne, Lin, Juei Jueng, Lynch, Timothy, Lichtner, Peter, Mellick, George D., Mok, Vincent, Morrison, Karin E., Quattrone, Aldo, Satake, Wataru, Silburn, Peter A., Stefanis, Leonidas, Stockton, Joanne D., Tan, Eng King, Toda, Tatsushi, Brice, Alexis, Van Broeckhoven, Christine, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Maraganore, Demetrius M., Gasser, Thomas, Krüger, Rejko, Farrer, Matthew J., Ross, Owen A., Sharma, Manu

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Association of α-synuclein Rep1 polymorphism and Parkinson's disease: Influence of Rep1 on age at onset by Hadjigeorgiou, Georgios M., Xiromerisiou, Georgia, Gourbali, Vanessa, Aggelakis, Kostantinos, Scarmeas, Nikolaos, Papadimitriou, Alexandros, Singleton, Andrew

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Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients by Clarimon, Jordi, Xiromerisiou, Georgia, Eerola, Johanna, Gourbali, Vanesa, Hellström, Olli, Dardiotis, Euthimios, Peuralinna, Terhi, Papadimitriou, Alexandros, Hadjigeorgiou, George M, Tienari, Pentti J, Singleton, Andrew B

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The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations by Scholz, Sonja W., Xiromerisiou, Georgia, Fung, Hon C., Eerola, Johanna, Hellström, Olli, Papadimitriou, Alexandros, Hadjigeorgiou, Georgios M., Tienari, Pentti J., Fernandez, Hubert H., Mandel, Ronald, Okun, Michael S., Gwinn-Hardy, Katharina, Singleton, Andrew B.

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Post-COVID-19 Parkinsonism and Parkinson's Disease Pathogenesis: The Exosomal Cargo Hypothesis by Mysiris, Dimitrios S, Vavougios, George D, Karamichali, Eirini, Papoutsopoulou, Stamatia, Stavrou, Vasileios T, Papayianni, Eirini, Boutlas, Stylianos, Mavridis, Theodoros, Foka, Pelagia, Zarogiannis, Sotirios G, Gourgoulianis, Konstantinos, Xiromerisiou, Georgia

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Sleep disorders and Alzheimer's disease pathophysiology: The role of the Glymphatic System. A scoping review by Astara, Kyriaki, Tsimpolis, Alexandros, Kalafatakis, Konstantinos, Vavougios, George D, Xiromerisiou, Georgia, Dardiotis, Efthimios, Christodoulou, Nikos G, Samara, Myrto T, Lappas, Andreas S

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Association between white matter lesions and Parkinson's disease: an impact on Postural/Gait difficulty phenotype and cognitive performance by Sinani, Olga, Dadouli, Katerina, Ntellas, Panagiotis, Kapsalaki, Eftychia Z, Vlychou, Marianna, Raptis, Dimitrios G, Marogianni, Chrysoula, Markou, Katerina, Dardiotis, Efthimios, Xiromerisiou, Georgia

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study by Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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