Πλοήγηση ανά Συγγραφέα "Aggelakis, K."
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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) -
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 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 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) -
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) -
IL-1RN and IL-1B gene polymorphisms and cerebral hemorrhagic events after traumatic brain injury
Hadjigeorgiou, G. M.; Paterakis, K.; Dardiotis, E.; Dardioti, M.; Aggelakis, K.; Tasiou, A.; Xiromerisiou, G.; Komnos, A.; Zintzaras, E.; Scarmeas, N.; Papadimitriou, A.; Karantanas, A. (2005)Objective: To investigate the association of (variable number tandem repeat) interleukin (IL) 1RN and (-511) IL-1B gene polymorphisms with brain hemorrhagic events after traumatic brain injury (TBI). Methods: Data from ... -
Increased frequency of white matter lesions in patients with osteonecrosis (WMLeON) of the femoral head
Hadjigeorgiou, G.; Aggelakis, K.; Dardiotis, E.; Zimbis, A.; Karantanas, A.; Papadimitriou, A.; Malizos, K. (2004) -
Interleukin 1 receptor antagonist (IL 1RN) and interleukin 1B (IL 1B) gene polymorphisms and primary intracerebral hemorrhage (ICH)
Dardiotis, E.; Dardioti, M.; Tasiou, A.; Aggelakis, K.; Paterakis, K.; Tsimourtou, V.; Noulas, G.; Komnos, A.; Karantanas, A.; Papadimitriou, A.; Hadjigeorgiou, G. (2005) -
Interleukin 1 receptor antagonist gene polymorphism and cerebral haemorrhagic events in patients with traumatic brain injury
Dardiotis, E.; Aggelakis, K.; Paterakis, K.; Tasiou, A.; Komnos, A.; Karantanas, A.; Dardioti, M.; Gabranis, I.; Papadimitriou, A.; Hadjigeorgiou, G. (2004) -
Interleukin 1 receptor antagonist gene polymorphism and traumatic brain injury
Dardiotis, E.; Aggelakis, K.; Paterakis, K.; Komnos, A.; Karantanas, A.; Tasiou, A.; Xiromerissiou, G.; Noulas, G.; Karavellis, A.; Papadimitriou, A.; Hadjigeorgiou, G. (2004) -
Interleukin 1a (-889) gene polymorphism and primary intracerebral hemorrhage
Dardiotis, E.; Dardioti, M.; Komnos, A.; Paterakis, K.; Tasiou, A.; Aggelakis, K.; Xiromerisiou, G.; Gabranis, J.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2007) -
Interleukin 2 (+114) gene polymorphism and traumatic brain injury
Dardioti, M.; Dardiotis, E.; Aggelakis, K.; Paterakis, K.; Komnos, A.; Karantanas, A.; Tasiou, A.; Xiromerisiou, G.; Hadjigeorgiou, G. (2006) -
Interleukin 2 (-384) gene polymorphism and traumatic brain injury
Dardioti, M.; Dardiotis, E.; Aggelakis, K.; Komnos, A.; Tasiou, A.; Paterakis, K.; Noulas, G.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2006) -
Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS
Aggelakis, K.; Zacharaki, F.; Dardiotis, E.; Xiromerisiou, G.; Tsimourtou, V.; Ralli, S.; Gkaraveli, M.; Bourpoulas, D.; Rodopoulou, P.; Papadimitriou, A.; Hadjigeorgiou, G. (2010)We investigated the association of specific polymorphisms of the interleukin IL-1b (AvaI -511 and TaqI +3,953) and IL-1 receptor antagonist (IL-1RN) (a variable number of tandem repeats; VNTR) genes with both the susceptibility ... -
Multiple sclerosis and autoimmune liver diseases
Aggelakis, K.; Tsimourtou, V.; Rigopoulou, E.; Noulas, G.; Dardiotis, E.; Dalekos, G.; Papadimitriou, A.; Hadjigeorgiou, G. (2005) -
Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease
Li, Y.; Rowland, C.; Xiromerisiou, G.; Lagier, R. J.; Schrodi, S. J.; Dradiotis, E.; Ross, D.; Bui, N.; Catanese, J.; Aggelakis, K.; Grupe, A.; Hadjigeorgiou, G. (2008)Susceptibility to sporadic Parkinson's diseases (PD) is thought to be influence by both genetic and environmental factors and thier interaction with each other. Statistical models including multiples variants in axon ... -
Paraoxonase 1 (PON1) gene polymorphisins (M55L and Q192R) and osteonecrosis of the femoral head with and without cerebral white matter lesions
Hadjigeorgiou, G. M.; Dardioti, M.; Dardiotis, E.; Aggelakis, K.; Xiromerisiou, G.; Tsimourtou, V.; Noulas, G.; Malizos, K.; Zimbis, A.; Papadimitriou, A.; Karantanas, A. (2005)