Browsing by Author "Paterakis, K."
Now showing items 21-23 of 23
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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 ... -
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) -
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)