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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Search
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Mutated alpha-synuclein gene in two Greek kindreds with familial PD: Incomplete penetrance? 

Papadimitriou, A.; Veletza, V.; Hadjigeorgiou, G. M.; Patrikiou, A.; Hirano, M.; Anastasopoulos, I. (1999)
The G209A mutation in the alpha-synuclein gene has been associated with autosomal dominant PD (ADPD) in a family from Contursi, Italy, and three apparently unrelated Greek families. Several groups around the world failed ...
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Novel Twinkle (PE01) gene mutations in mendelian progressive external ophthalmoplegia 

Virgilio, R.; Ronchi, D.; Hadjigeorgiou, G. M.; Bordoni, A.; Saladino, F.; Moggio, M.; Adobbati, L.; Kafetsouli, D.; Tsironi, E.; Previtali, S.; Papadimitriou, A.; Bresolin, N.; Comi, G. P. (2008)
Multiple deletions of mitochondrial DNA (mtDNA) are associated with different mitochondrial disorders inherited as autosomal dominant and recessive traits. Causative mutations have been found in five genes, mainly involved ...
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Lack of Association of the UCHL-1 Gene with Parkinson's Disease in a Greek Cohort: A Haplotype-Tagging Approach 

Xiromerisiou, G.; Kyratzi, E.; Dardiotis, E.; Bozi, M.; Tsimourtou, V.; Stamboulis, E.; Ralli, S.; Vassilatis, D.; Gourbali, V.; Kountra, P. M.; Fountas, K.; Papadimitriou, A.; Stefanis, L.; Hadjigeorgiou, G. M. (2011)
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Mutated α-synuclein gene in two greek kindreds with familial pd: Incomplete penetrance? 

Papadimitriou, A.; Veletza, V.; Hadjigeorgiou, G. M.; Patrikiou, A.; Hirano, M.; Anastasopoulos, I. (1999)
The G209A mutation in the α-synuclein gene has been associated with autosomal dominant PD (ADPD) in a family from Contursi, Italy, and three apparently unrelated Greek families. Several groups around the world failed to ...
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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 ...
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Protein misfolding in neurodegenerative diseases 

Agorogiannis, E. I.; Agorogiannis, G. I.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2004)
A common pathogenic mechanism shared by diverse neurodegenerative disorders, like Alzheimer's disease, Parkinson's disease, Huntington's disease and transmissible spongiform encephalopathies, may be altered protein homeostasis ...
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Genetic and molecular pathogenesis of Parkinson's disease 

Agorogiannis, E. I.; Agorogiannis, G. I.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2006)
Parkinson's disease (PD), a common progressive degenerative disease of the central nervous system, affects about 1% of adults aged older than 60 years. PD is characterized by rigidity, tremor, postural instability and ...
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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 ...
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Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants 

Xiromerisiou, G.; Hadjigeorgiou, G. M.; Gourbali, V.; Johnson, J.; Papakonstantinou, I.; Papadimitriou, A.; Singleton, A. B. (2007)
Mutations in SNCA and LRRK2 genes, encoding alpha-synuclein and leucine-rich repeat kinase 2, respectively, cause autosomal dominant Parkinson's disease (AdPD). The LRRK2 G2019S (c.6055G > A) and R1441G (c.4321C > G) ...
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Positron emission tomography changes in PARK1 mutation 

Perani, D.; Garibotto, V.; Hadjigeorgiou, G. M.; Papadimitriou, D.; Fazio, F.; Papadimitriou, A. (2006)
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Hadjigeorgiou, G. M. (31)
Papadimitriou, A. (31)
Xiromerisiou, G. (14)Dardiotis, E. (11)Aggelakis, K. (8)Dardioti, M. (8)Paterakis, K. (8)Komnos, A. (7)Tasiou, A. (7)Gourbali, V. (6)Singleton, A. B. (6)Eerola, J. (4)Hellstrom, O. (4)Noulas, G. (4)Tienari, P. J. (4)Bordoni, A. (3)Bresolin, N. (3)Comi, G. P. (3)DiMauro, S. (3)Hirano, M. (3)... View MoreSubjectClinical Neurology (23)Neurosciences (18)Parkinson's disease (8)ALPHA-SYNUCLEIN GENE (4)ASSOCIATION (4)human (3)PARKINSONS-DISEASE (3)alpha synuclein (2)article (2)clinical article (2)... View MoreDate Issued2010 - 2014 (3)2000 - 2009 (26)1999 - 1999 (2)Has File(s)No (31)
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