Georgia Xiromerisiou

Georgia Xiromerisiou

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Georgia Xiromerisiou

Georgia Xiromerisiou

Publications by authors named "Georgia Xiromerisiou"

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Motor function and the probability of prodromal Parkinson's disease in older adults.

Mov Disord 2019 Sep 17;34(9):1345-1353. Epub 2019 Jul 17.

1st Department of Neurology, Aiginition Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece.

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http://dx.doi.org/10.1002/mds.27792DOI Listing
September 2019

Higher probability of prodromal Parkinson disease is related to lower cognitive performance.

Neurology 2019 May 3;92(19):e2261-e2272. Epub 2019 Apr 3.

From the 1st Department of Neurology (A.B., E.N., C.A.A., L.S., N.S.), Aiginition Hospital, National and Kapodistrian, University of Athens Medical School; Department of Nutrition and Dietetics (M.I.M., M.Y., E.N., C.A.A.), Harokopio University; Parkinson's Disease and Movement Disorders Department (M.S.), Hygeia Hospital, Athens, Greece; Department of Neurology (M.S.), Philipps University, Marburg, Germany; School of Medicine (G.X., E.D., G.M.H.), University of Thessaly, Larissa; Laboratory of Cognitive Neuroscience, School of Psychology (M.H.K.), Aristotle University of Thessaloniki, Greece; Department of Neurology (G.M.H.), Medical School, University of Cyprus; Athens Association of Alzheimer's Disease and Related Disorders (E.N., P.S.), Maroussi; Center of Clinical, Experimental Surgery and Translational Research (L.S.), Biomedical Research Foundation of the Academy of Athens, Greece; and Taub Institute for Research in Alzheimer's Disease and the Aging Brain (N.S.), The Gertrude H. Sergievsky Center, Department of Neurology, Columbia University, New York, NY.

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http://dx.doi.org/10.1212/WNL.0000000000007453DOI Listing
May 2019

Mediterranean diet adherence is related to reduced probability of prodromal Parkinson's disease.

Mov Disord 2019 01 10;34(1):48-57. Epub 2018 Oct 10.

1st Department of Neurology, Aiginition Hospital, National and Kapodistrian University of Athens Medical School, Greece.

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http://dx.doi.org/10.1002/mds.27489DOI Listing
January 2019

Periodic Paralysis and Encephalopathy as Initial Manifestations of Graves' Disease: Case Report and Review of the Literature.

Neurologist 2017 Jul;22(4):134-137

*Neurology Department, Papageorgiou General Hospital ‡Department of Medicine, Second Medical Clinic, Aristotle University of Thessaloniki, Ippokration Hospital, Thessaloniki, Greece †Department of Clinical Neurophysiology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.

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http://dx.doi.org/10.1097/NRL.0000000000000125DOI Listing
July 2017

A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature.

Neurobiol Aging 2017 05 20;53:194.e13-194.e22. Epub 2017 Jan 20.

Department of Neurology, University of Thessaly, University Hospital of Larissa, Larissa, Greece; Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, Larissa, Greece. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.01.015DOI Listing
May 2017

Helicobacter pylori on portal hypertension-related hepatic encephalopathy.

Immunopharmacol Immunotoxicol 2017 Apr 10;39(2):105-106. Epub 2017 Feb 10.

a Department of Medicine , Second Medical Clinic, Aristotle University of Thessaloniki, Ippokration Hospital , Thessaloniki , Greece.

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http://dx.doi.org/10.1080/08923973.2017.1286503DOI Listing
April 2017

Genetic and phenotypic characterization of complex hereditary spastic paraplegia.

Brain 2016 07 23;139(Pt 7):1904-18. Epub 2016 May 23.

1 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Alzheimer's Disease Research Centre, Department of Neurology, Harvard Medical School and Massachusetts General Hospital, 114 16th Street, Charlestown, MA 02129, USA

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http://dx.doi.org/10.1093/brain/aww111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939695PMC
July 2016

The clinical and genetic heterogeneity of paroxysmal dyskinesias.

Brain 2015 Dec 23;138(Pt 12):3567-80. Epub 2015 Nov 23.

1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 4 Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK

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http://dx.doi.org/10.1093/brain/awv310DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655345PMC
December 2015

Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis.

J Neurol Sci 2014 Apr 1;339(1-2):220-2. Epub 2014 Feb 1.

Department of Molecular Neuroscience, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK; MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK.

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http://dx.doi.org/10.1016/j.jns.2014.01.034DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988988PMC
April 2014

TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT.

Neurobiol Aging 2013 Dec 9;34(12):2889.e5-9. Epub 2013 May 9.

Reta Lila Weston Institute of Neurological Studies and Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906605PMC
December 2013

The syndrome of deafness-dystonia: clinical and genetic heterogeneity.

Mov Disord 2013 Jun 15;28(6):795-803. Epub 2013 Feb 15.

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, United Kingdom.

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http://dx.doi.org/10.1002/mds.25394DOI Listing
June 2013

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

J Med Genet 2012 Nov;49(11):721-6

Department. of Neurodegenerative diseases, Hertie-Institute for Clinical Brain Research and DZNE- German Center for Neurodegenerative Diseases, Tübingen, Hoppe-Seyler-Str. 3, Tübingen 72076, Germany.

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http://dx.doi.org/10.1136/jmedgenet-2012-101155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488700PMC
November 2012

THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.

Mov Disord 2012 Sep 17;27(10):1290-4. Epub 2012 Aug 17.

Department of Molecular Neuroscience and Reta Lila Weston Institute, University College London Institute of Neurology, London, London, United Kingdom; Department of Neurology, Faculty of Medicine University of Thessaly, Larissa, Greece.

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http://dx.doi.org/10.1002/mds.25146DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3664430PMC
September 2012

Angiotensin-converting enzyme tag single nucleotide polymorphisms in patients with intracerebral hemorrhage.

Pharmacogenet Genomics 2011 Mar;21(3):136-41

Department of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, Larissa, Greece.

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http://dx.doi.org/10.1097/FPC.0b013e328343ab15DOI Listing
March 2011

Genetic basis of Parkinson disease.

Neurosurg Focus 2010 Jan;28(1):E7

Institute for Biomedical Technology (BIOMED), Centre for Research and Technology-Thessaly (CERETETH), Larussa, Greece.

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http://dx.doi.org/10.3171/2009.10.FOCUS09220DOI Listing
January 2010

Genetic association studies in patients with traumatic brain injury.

Neurosurg Focus 2010 Jan;28(1):E9

Department of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, Larissa, Greece.

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http://dx.doi.org/10.3171/2009.10.FOCUS09215DOI Listing
January 2010

Acute bilateral thalamic infarction as a cause of acute dementia and hypophonia after occlusion of the artery of Percheron.

J Neurol Sci 2009 Aug 13;283(1-2):175-7. Epub 2009 May 13.

1st Department of Neurology, Aristotelian University, School of Medicine, Agriteli 4, 55132, Thessaloniki, Greece.

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http://dx.doi.org/10.1016/j.jns.2009.02.369DOI Listing
August 2009

Association between AKT1 gene and Parkinson's disease: a protective haplotype.

Neurosci Lett 2008 May 15;436(2):232-4. Epub 2008 Mar 15.

University of Thessaly, Medical School, Department of Neurology, Neurogenetics Unit, Papakyriazi 22 Street, Larissa 41222, Greece.

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http://dx.doi.org/10.1016/j.neulet.2008.03.026DOI Listing
May 2008

Association of alpha-synuclein Rep1 polymorphism and Parkinson's disease: influence of Rep1 on age at onset.

Mov Disord 2006 Apr;21(4):534-9

Neurogenetics Unit, Department of Neurology, Medical School, University of Thessaly, Larissa, Greece.

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http://dx.doi.org/10.1002/mds.20752DOI Listing
April 2006

The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.

Neurosci Lett 2006 Mar 18;395(3):227-9. Epub 2005 Nov 18.

Molecular Genetics Unit, National Institute on Aging, National Institutes of Health, Building 35, Room 1A-1012, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.neulet.2005.10.081DOI Listing
March 2006

How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease.

Curr Opin Neurol 2005 Dec;18(6):706-11

Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland 20982-3707, USA.

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December 2005