Search filters

List of works by Georgia Xiromerisiou

A Prospective Validation of the Updated Movement Disorders Society Research Criteria for Prodromal Parkinson's Disease

scientific article published on 22 June 2020

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

scientific article

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

scientific article

A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases

scientific article published on 07 November 2019

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

scientific article published on 20 January 2017

A novel task-specific dystonia type: Hemifacial spasm in a photographer

scientific article published on 06 November 2020

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene

scientific article published on 02 December 2009

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

scientific article published on 13 May 2009

Alpha-1 antichymotrypsin gene signal peptide a/t polymorphism and primary intracerebral hemorrhage

scientific article

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

scientific article published on 01 March 2011

Assessment of Parkinson's disease risk loci in Greece

scientific article published on 27 September 2013

Assessment of the reporting quality of double-blind RCTs for ischemic stroke based on the CONSORT statement

scientific article published on 27 May 2020

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

scientific article

Association between Helicobacter pylori infection and Guillain-Barré Syndrome: A meta-analysis

scientific article published on 02 March 2020

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

scientific article published on 01 April 2006

Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts

scientific article published on 01 January 2006

Autoantibodies to alpha-synuclein in inherited Parkinson's disease.

scientific article

BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groups

scientific article published on 30 December 2006

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases

scientific article published on 11 May 2020

Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia

scientific article published on 26 September 2020

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study

scientific article

Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease

scientific article published on 5 January 2012

Familial case of speech-induced tongue-protrusion dystonia

scientific article published on 06 February 2013

Frailty and prodromal Parkinson's disease: Results from the HELIAD study

scientific article published on 06 August 2020

Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset

scientific article

Genetic and phenotypic characterization of complex hereditary spastic paraplegia

scientific article published on 23 May 2016

Genetic association studies in patients with traumatic brain injury

scientific article published on January 2010

Genetic basis of Parkinson disease

scientific article published in January 2010

Genetic variations in the SULF1 gene alter the risk of cervical cancer and precancerous lesions

scientific article published on 06 July 2018

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

scientific article published on 8 December 2017

Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia.

scientific article published on 2 November 2017

Helicobacter pylori on portal hypertension-related hepatic encephalopathy

scientific article published on 10 February 2017

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

scientific article published on 03 April 2019

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

scientific article

IL-1RN and IL-1B gene polymorphisms and cerebral hemorrhagic events after traumatic brain injury

scientific article

Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease

scientific article

Impact of reactive oxygen species generation on Helicobacter pylori-related extragastric diseases: a hypothesis.

scientific article published on 17 January 2017

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

scientific article

Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS.

scientific article published on 30 October 2009

Lack of association of the UCHL-1 gene with Parkinson's disease in a Greek cohort: a haplotype-tagging approach

scientific article published on 28 May 2011

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

scientific article

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

scientific article

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

scientific article (publication date: September 2014)

Large-scale replication and heterogeneity in Parkinson disease genetic loci

scientific article

Low RLS prevalence and awareness in central Greece: an epidemiological survey

scientific article published in November 2007

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

scientific article published on 10 October 2018

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

scientific article published on 17 July 2019

Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease

scientific article

Neurodegeneration and Inflammation-An Interesting Interplay in Parkinson's Disease

scientific article published on 10 November 2020

New molecular diagnostic trends and biomarkers for amyotrophic lateral sclerosis

scientific article published on 21 January 2019

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

scientific article published on February 2014

Organochlorine pesticide levels in Greek patients with Parkinson's disease

scientific article published on 08 April 2020

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

scientific article

Posterior reversible encephalopathy in a GT1a positive oculopharyngeal variant of Guillain-Barré syndrome: A case-report and review of the literature

scientific article published on 22 June 2020

Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS

scientific article published on 26 April 2020

Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

scientific article published on 17 August 2013

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants

scientific article published on 01 January 2007

Screening for the C9ORF72 expansion in Greek Huntington Disease phenocopies and controls and meta-analysis of current data

scientific article published on 12 June 2020

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

scientific article

THAP1 mutations and dystonia phenotypes: genotype phenotype correlations

scientific article published on 17 August 2012

THAP1 mutations in a Greek primary blepharospasm series

scientific article

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium

scientific article published in February 2006

The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features

scientific article published on 16 May 2012

The clinical and genetic heterogeneity of paroxysmal dyskinesias

scientific article

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

article

The interplay between environmental and genetic factors in Parkinson's disease susceptibility: the evidence for pesticides.

scientific article published on 04 January 2013

The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database

scientific article published on 24 April 2019

The syndrome of deafness-dystonia: clinical and genetic heterogeneity

scientific article published on 15 February 2013

β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease

scientific article published on 24 June 2011

Paulina is supported by:

About Paulina

Help