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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases.
Xiromerisiou G, Marogianni C, Dadouli K, Zompola C, Georgouli D, Provatas A, Theodorou A, Zervas P, Nikolaidou C, Stergiou S, Ntellas P, Sokratous M, Stathis P, Paraskevas GP, Bonakis A, Voumvourakis K, Hadjichristodoulou C, Hadjigeorgiou GM, Tsivgoulis G. Xiromerisiou G, et al. Among authors: hadjigeorgiou gm. Neurol Genet. 2020 May 11;6(3):e434. doi: 10.1212/NXG.0000000000000434. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32582863 Free PMC article. Review.
Autoantibodies to alpha-synuclein in inherited Parkinson's disease.
Papachroni KK, Ninkina N, Papapanagiotou A, Hadjigeorgiou GM, Xiromerisiou G, Papadimitriou A, Kalofoutis A, Buchman VL. Papachroni KK, et al. Among authors: hadjigeorgiou gm. J Neurochem. 2007 May;101(3):749-56. doi: 10.1111/j.1471-4159.2006.04365.x. J Neurochem. 2007. PMID: 17448146 Free PMC article.
Association between AKT1 gene and Parkinson's disease: a protective haplotype.
Xiromerisiou G, Hadjigeorgiou GM, Papadimitriou A, Katsarogiannis E, Gourbali V, Singleton AB. Xiromerisiou G, et al. Among authors: hadjigeorgiou gm. Neurosci Lett. 2008 May 9;436(2):232-4. doi: 10.1016/j.neulet.2008.03.026. Epub 2008 Mar 15. Neurosci Lett. 2008. PMID: 18395980 Free PMC article.
Genetic association studies in patients with traumatic brain injury.
Dardiotis E, Fountas KN, Dardioti M, Xiromerisiou G, Kapsalaki E, Tasiou A, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: hadjigeorgiou gm. Neurosurg Focus. 2010 Jan;28(1):E9. doi: 10.3171/2009.10.FOCUS09215. Neurosurg Focus. 2010. PMID: 20043724 Review.
THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.
Xiromerisiou G, Houlden H, Scarmeas N, Stamelou M, Kara E, Hardy J, Lees AJ, Korlipara P, Limousin P, Paudel R, Hadjigeorgiou GM, Bhatia KP. Xiromerisiou G, et al. Among authors: hadjigeorgiou gm. Mov Disord. 2012 Sep 1;27(10):1290-4. doi: 10.1002/mds.25146. Epub 2012 Aug 17. Mov Disord. 2012. PMID: 22903657 Free PMC article. Review.
265 results