Restless legs syndrome does not affect 3-year mortality in hemodialysis patients von Stefanidis, I, Vainas, A, Giannaki, C.D, Dardiotis, E, Spanoulis, A, Sounidaki, M, Eleftheriadis, T, Liakopoulos, V, Karatzaferi, C, Sakkas, G.K, Zintzaras, E, Hadjigeorgiou, G.M

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Restless legs syndrome in hemodialysis patients: an epidemiologic survey in Greece von Stefanidis, I, Vainas, A, Dardiotis, E, Giannaki, C.D, Gourli, P, Papadopoulou, D, Vakianis, P, Patsidis, E, Eleftheriadis, T, Liakopoulos, V, Pournaras, S, Sakkas, G.K, Zintzaras, E, Hadjigeorgiou, G.M

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Restless legs syndrome and mortality in hemodialysis patients von Stefanidis, I, Vainas, A, Giannaki, C.D, Dardiotis, E, Spanoulis, A, Sounidaki, M, Eleftheriadis, T, Liakopoulos, V, Karatzaferi, C, Sakkas, G.K, Zintzaras, E, Hadjigeorgiou, G.M

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Investigation of Unmedicated Early Onset Restless Legs Syndrome by Voxel-Based Morphometry, T2 Relaxometry, and Functional MR Imaging during the Night-Time Hours von MARGARITI, P. N, ASTRAKAS, L. G, TSOULI, S. G, HADJIGEORGIOU, G. M, KONITSIOTIS, S, ARGYROPOULOU, M. I

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Motor signs during the course of Alzheimer disease von SCARMEAS, N, HADJIGEORGIOU, G. M, WEGESIN, D, STERN, Y, PAPADIMITRIOU, A, DUBOIS, B, SARAZIN, M, BRANDT, J, ALBERT, M, MARDER, K, BELL, K, HONIG, L. S

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Mutated α-synuclein gene in two Greek kindreds with familial PD : Incomplete penetrance? von PAPADIMITRIOU, A, VELETZA, V, HADJIGEORGIOU, G. M, PATRIKIOU, A, HIRANO, M, ANASTASOPOULOS, I

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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 von 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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BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groups von 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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Alpha-1 Antichymotrypsin Gene Signal Peptide A/T Polymorphism and Primary Intracerebral Hemorrhage von Dardiotis, E., Hadjigeorgiou, G.M., Dardioti, M., Scarmeas, N., Paterakis, K., Aggelakis, K., Komnos, A., Tasiou, A., Xiromerisiou, G., Gabranis, I., Zintzaras, E., Papadimitriou, A., Karantanas, A.

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Association of Tau Haplotype-Tagging Polymorphisms with Parkinson’s Disease in Diverse Ethnic Parkinson’s Disease Cohorts von Fung, H.C., Xiromerisiou, G., Gibbs, J.R., Wu, Y.R., Eerola, J., Gourbali, V., Hellström, O., Chen, C.M., Duckworth, J., Papadimitriou, A., Tienari, P.J., Hadjigeorgiou, G.M., Hardy, J., Singleton, A.B.

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Primary Sjögren syndrome‐related peripheral neuropathy: a systematic review and meta‐analysis von Liampas, A, Parperis, K, Erotocritou, M.F, Nteveros, A, Papadopoulou, M, Moschovos, C, Akil, M, Coaccioli, S, Hadjigeorgiou, G.M, Hadjivassiliou, M, Zis, P

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EEG recordings as biomarkers of pain perception: where do we stand and where to go? von Zis, P, Liampas, A, Artemiadis, A, Tsalamandris, G, Neophytou, P, Unwin, Z, Kimiskidis, V.K, Hadjigeorgiou, G.M, Varrassi, G, Zhao, Y, Sarrigiannis, P.G

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The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism von Papadimitriou, A, Hadjigeorgiou, G M, Divari, R, Papagalanis, N, Comi, G, Bresolin, N

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Supplementary Material for: The Hellenic Longitudinal Investigation of Aging and Diet (HELIAD): Rationale, Study Design, and Cohort Description von Dardiotis, E., Kosmidis, M.H., Yannakoulia, M., Hadjigeorgiou, G.M., Scarmeas, N.

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A new mitochondrial DNA mutation (A3288G) in the tRNA Leu(UUR) gene associated with familial myopathy von Hadjigeorgiou, G.M., Kim, S.H., Fischbeck, K.H., Andreu, A.L., Berry, G.T., Bingham, P., Shanske, S., Bonilla, E., DiMauro, S.

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A new mitochondrial DNA mutation (A3288g) in the tRNALeu(UUR) gene associated with familial myopathy von HADJIGEORGIOU, G. M, KIM, S. H, FISCHBECK, K. H, ANDREU, A. L, BERRY, G. T, BINGHAM, P, SHANSKE, S, BONILLA, E, DIMAURO, S

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The influence of coenzyme Q 10 on total serum calcium concentration in two patients with kearns-sayre syndrome and hypoparathyroidism von Papadimitriou, A., Hadjigeorgiou, G.M., Divari, R., Papagalanis, N., Comi, G., Bresolin, N.

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