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Tumor necrosis factor-a(-308) gene polymorphism and traumatic brain injury

Dardiotis, E.; Dardioti, M.; Aggelakis, K.; Komnos, A.; Tasiou, A.; Paterakis, K.; Ralli, S.; Xiromerisiou, G.; Gabranis, J.; Papadimitriou, A.; Hadjigeorgiou, G. M. (2007)

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)

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)

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)

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)

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

Hadjigeorgiou, G. M.; Stefanidis, I.; Dardiotis, E.; Aggellakis, K.; Sakkas, G. K.; Xiromerisiou, G.; Konitsiotis, S.; Paterakis, K.; Poultsidi, A.; Tsimourtou, V.; Ralli, S.; Gourgoulianis, K.; Zintzaras, E. (2007)

Restless legs syndrome (RLS) is a sensorimotor disorder with a general population prevalence of 3-10%. A single, previous epidemiological study performed in southeast Europe reported the lowest prevalence rate amongst ...

A new stop codon mutation (Y52X) in the myophosphorylase gene in a Greek patient with McArdle's disease

Hadjigeorgiou, G. M.; Papadimitriou, A.; Musumeci, O.; Paterakis, K.; Flabouriari, K.; Shanske, S.; DiMauro, S. (2002)

We identified a novel stop codon mutation in the myophosphorylase gene in a Greek patient with typical symptoms of McArdle's disease. This is the first genetic study of myophosphorylase deficiency in a Greek family, showing ...

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 ...

Re: Lack of association between the IL-1 gene (-889) polymorphism and outcome after head injury ( Tanriverdi T, et al. Surgical Neurology 2006;65 : 7-10)

Dardiotis, E.; Dardioti, M.; Hadjigeorgiou, G. M.; Paterakis, K. (2006)

AQP4 Tag Single Nucleotide Polymorphisms in Patients with Traumatic Brain Injury

Dardiotis, E.; Paterakis, K.; Tsivgoulis, G.; Tsintou, M.; Hadjigeorgiou, G. F.; Dardioti, M.; Grigoriadis, S.; Simeonidou, C.; Komnos, A.; Kapsalaki, E.; Fountas, K.; Hadjigeorgiou, G. M. (2014)

Accumulating evidence suggests that the extent of brain injury and the clinical outcome after traumatic brain injury (TBI) are modulated, to some degree, by genetic variants. Aquaporin-4 (AQP4) is the predominant water ...