Πλοήγηση ανά Συγγραφέα "Papadimitriou, A."

A1-antichymotrypsin gene polymorphism and cerebral hemorrhagic events in patients with traumatic brain injury

Dardioti, M.; Dardiotis, E.; Aggelakis, K.; Tasiou, A.; Paterakis, K.; Komnos, A.; Karantanas, A.; Xiromerisiou, G.; Papadimitriou, A.; Hadjigeorgiou, G. (2005)

A1-antichymotrypsin gene polymorphism and primary intracerebral hemorrhage (ICH)

Dardiotis, E.; Dardioti, M.; Aggelakis, K.; Komnos, A.; Noulas, G.; Paterakis, K.; Tasiou, A.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2006)

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

Daiou, C.; Christodoulou, K.; Xiromerisiou, G.; Panas, M.; Dardiotis, E.; Kladi, A.; Speletas, M.; Ntaios, G.; Papadimitriou, A.; Germenis, A.; Hadjigeorgiou, G. M. (2010)

Phenotype of patients with the aprataxin gene mutation varies and according to previous studies, screening of aprataxin gene could be useful, once frataxin gene mutation is excluded in patients with normal GAA expansion ...

Alpha-1 antichymotrypsin gene signal peptide A/T polymorphism and primary intracerebral hemorrhage

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. (2008)

Background/Aims: Alpha-1 antichymotrypsin (ACT), a serine proteinase inhibitor, has been implicated in vascular pathology. The TT genotype of the ACT signal peptide A/T polymorphism has been reported to confer susceptibility ...

Angiotensin converting enzyme (ACE) I/D gene polymorphism and primary intracerebral hemorrhage (ICH)

Dardiotis, E.; Dardioti, M.; Aggelakis, K.; Komnos, A.; Noulas, G.; Paterakis, K.; Tasiou, A.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2006)

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

Xiromerisiou, G.; Hadjigeorgiou, G. M.; Papadimitriou, A.; Katsarogiannis, E.; Gourbali, V.; Singleton, A. B. (2008)

Variation in AKT1 has been associated with schizophrenia, bipolar disease and type 11 diabetes. The aim of the present study was to investigate the potential role of variability within AKT1 as a risk factor for Parkinson's ...

Association between PIK3C2B gene and Parkinson's disease: evidence for involvement of the PI3K/AKT pathway

Xiromerisiou, G.; Dardiotis, E.; Kountra, P.; Patramani, I.; Vogiatzi, C.; Katsavaki, M.; Tsimourtou, V.; Ralli, S.; Markou, K.; Papadimitriou, A.; Hadjigeorgiou, G. (2010)

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

Xiromerisiou, G.; Gourbali, V.; Aggelakis, K.; Dardiotis, E.; Tsimourtou, V.; Papadimitriou, A.; Papakonstantinou, I.; Scarmeas, N.; Singleton, A.; Hadjigeorgiou, G. (2005)

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

Fung, H. C.; Xiromerisiou, G.; Gibbs, J. R.; Wu, Y. R.; Eerola, J.; Gourbali, V.; Hellstrom, O.; Chen, C. M.; Duckworth, J.; Papadimitriou, A.; Tienari, P. J.; Hadjigeorgiou, G. M.; Hardy, J.; Singleton, A. B. (2006)

Background: The overlap in the clinical and pathological features of tauopathies and synucleinopathies raises the possibility that the tau protein may be important in Parkinson's disease (PD) pathogenesis. Several MAPT ...

Association of tumor necrosis factor-alpha gene polymorphism (-308) and obstructive sleep apnea-hypopnea syndrome

Almpanidou, P.; Hadjigeorgiou, G.; Gourgoulianis, K.; Papadimitriou, A. (2012)

Background and Aim: Elevated serum tumor necrosis factor-alpha (TNF-alpha) concentration and a polymorphism of the TNF-alpha gene at the position -308 in the promoter region are associated with obstructive sleep apnea-hypopnea ...

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

Hadjigeorgiou, G. H.; Xiromerisiou, G.; Gourbali, V.; Aggelakis, K.; Scarmeas, N.; Papadimitriou, A.; Singleton, A. (2006)

The α-synuclein Rep1 polymorphism was studied in patients and controls in an ethnic Greek population. There was an association of allele 2 with risk of Parkinson's disease (PD; adjusted odd ratio = 3.25; 95% CI = 1.80-5.87). ...

Association study of (VNTR) 1L-1RN and (-511) IL-1B gene polymorphisms and cerebral haemorrhagic events in patients with traumatic brain injury

Hadjigeorgiou, G.; Dardiotis, E.; Paterakis, K.; Dardioti, M.; Aggelakis, K.; Tasiou, A.; Xiromerisiou, G.; Karantanas, A.; Komnos, A.; Zintzaras, E.; Scarmeas, N.; Papadimitriou, A. (2005)

Autoantibodies to alpha-synuclein in inherited Parkinson's disease

Papachroni, K. K.; Ninkina, N.; Papapanagiotou, A.; Hadjigeorgiou, G. M.; Xiromerisiou, G.; Papadimitriou, A.; Kalofoutis, A.; Buchman, V. L. (2007)

Neurodegeneration in Parkinson's disease (PD) is accompanied by a local immune reaction in the affected brain regions. It is well established that alpha-synuclein is directly implicated in the pathogenesis of PD. Development ...

BDNF haplotype tagging SNPs in Greek sporadic PD patients and patterns of linkage disequilibrium

Xiromerisiou, G.; Tsimourtou, V.; Gourbali, V.; Aggelakis, K.; Dardiotis, E.; Dardioti, M.; Noulas, G.; Papadimitriou, A.; Singleton, A.; Hadjigeorgiou, G. (2006)

Behavioral abnormalities predict poor cognitive and functional outcomes and institutionalization in Alzheimer's disease (AD)

Scarmeas, N.; Hadjigeorgiou, G.; Papadimitriou, A.; Dubois, B.; Sarazin, M.; Brandt, J.; Blacker, D.; Albert, M.; Devanand, D.; Honig, L.; Marder, K.; Bell, K.; Stern, Y. (2005)

Brain MRI and proton MRS findings in infants and children with respiratory chain defects

Dinopoulos, A.; Cecil, K. M.; Schapiro, M. B.; Papadimitriou, A.; Hadjigeorgiou, G. M.; Wong, B.; DeGrauw, T.; Egelhoff, J. C. (2005)

Objective: The aim of this study is to describe neuroimaging patterns in children with respiratory chain (RC) defects using magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (MRS) and to assess ...

Charcot-Marie-Tooth Disease in Cyprus: Epidemiological, Clinical and Genetic Characteristics

Nicolaou, P.; Zamba-Papanicolaou, E.; Koutsou, P.; Kleopa, K. A.; Georghiou, A.; Hadjigeorgiou, G.; Papadimitriou, A.; Kyriakides, T.; Christodoulou, K. (2010)

Background: Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy. CMT is classified into 2 main subgroups: a demyelinating and an axonal type. Further subdivisions within these 2 main categories exist ...

Clinical phenotype in patients with α-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease

Papapetropoulos, S.; Paschalis, C.; Athanassiadou, A.; Papadimitriou, A.; Ellul, J.; Polymeropoulos, M. H.; Papapetropoulos, Th (2001)

Objective - An Ala53Thr mutation of the α-synuclein gene has been recently identified as a rare cause of autosomal Parkinson's disease (PD). The clinical characteristics of 15 patients with PD living in Greece with the ...

Continuous muscle fiber activity associated with morphea (localized scleroderma)

Papadimitriou, A.; Chroni, E.; Anastasopoulos, I.; Avramidis, T.; Hadjigeorgiou, G.; Koutroumanidis, M. (1998)

Delusions and hallucinations are associated with worse outcome in Alzheimer disease

Scarmeas, N.; Brandt, J.; Albert, M.; Hadjigeorgiou, G.; Papadimitriou, A.; Dubois, B.; Sarazin, M.; Devanand, D.; Honig, L.; Marder, K.; Bell, K.; Wegesin, D.; Blacker, D.; Stern, Y. (2005)

Background: Delusions and hallucinations are common in Alzheimer disease (AD) and there are conflicting reports regarding their ability to predict cognitive decline, functional decline, and institutionalization. According ...