14 results for author:"Pera J." in Literature citations
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| APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study. International Stroke Genetics Consortium Lancet Neurol 10:702-709(2011) · Mapped (5) |
| The rs2200733 variant on chromosome 4q25 is a risk factor for cardioembolic stroke related to atrial fibrillation in Polish patients. Wnuk M., Pera J., Jagiella J., Szczygiel E., Ferens A., Spisak K., Wolkow P., Kmiec M., Burkot J., Chrzanowska-Wasko J. et al. Neurol. Neurochir. Pol. 45:148-152(2011) · Mapped (2) |
| Interleukin 6-174G>C polymorphism and risk of aneurysmal subarachnoid hemorrhage: case-control study and meta-analysis. Pera J., Dziedzic T., Adamski M., Jagiella J., Krupa M., Moskala M., Szczudlik A., Slowik A. Acta Neurol. Scand. 125:111-115(2012) · Mapped (5) |
| The C(-1562)T polymorphism of the MMP-9 gene and the risk of sporadic amyotrophic lateral sclerosis. Zawislak D., Borratynska A., Tomik B., Pera J., Gryz-Kurek E., Szczudlik A. Neurol. Neurochir. Pol. 43:121-125(2009) · Mapped (7) |
| Glutathione peroxidase 1 C593T polymorphism is associated with lobar intracerebral hemorrhage. Pera J., Slowik A., Dziedzic T., Pulyk R., Wloch D., Szczudlik A. Cerebrovasc. Dis. 25:445-449(2008) · Mapped (3) |
| Paraoxonase 2 gene C311S polymorphism is associated with a risk of large vessel disease stroke in a Polish population. Slowik A., Wloch D., Szermer P., Wolkow P., Malecki M., Pera J., Turaj W., Dziedzic T., Klimkowicz-Mrowiec A., Kopec G. et al. Cerebrovasc. Dis. 23:395-400(2007) · Mapped (9) |
| Paraoxonase gene polymorphisms and sporadic ALS. Slowik A., Tomik B., Wolkow P.P., Partyka D., Turaj W., Malecki M.T., Pera J., Dziedzic T., Szczudlik A., Figlewicz D.A. Neurology 67:766-770(2006) · Mapped (11) |
| SERPINA3 polymorphism is not associated with primary intracerebral hemorrhage in a Polish population. Pera J., Slowik A., Dziedzic T., Szczudlik A. Stroke 37:906-907(2006) · Mapped (4) |
| Interleukin 1 beta polymorphism (-511) and risk of stroke due to small vessel disease. Dziedzic T., Slowik A., Pera J., Szczudlik A. Cerebrovasc. Dis. 20:299-303(2005) · Mapped (3) |
| Endoglin gene insertion polymorphism not associated with aneurysmal subarachnoid hemorrhage. Pera J., Slowik A., Dziedzic T., Borratynska A., Rog T.M., Betlej M., Czepko R., Szczudlik A. J. Neurosurg. 102:879-881(2005) · Mapped (9) |
| Alpha1-antichymotrypsin gene (SERPINA3) A/T polymorphism as a risk factor for aneurysmal subarachnoid hemorrhage. Slowik A., Borratynska A., Turaj W., Pera J., Dziedzic T., Figlewicz D.A., Betlej M., Krzyszkowski T., Czepko R., Szczudlik A. Stroke 36:737-740(2005) · Mapped (4) |
| Coagulation factor XIII VaI34Leu polymorphism in patients with small vessel disease or primary intracerebral hemorrhage. Slowik A., Dziedzic T., Pera J., Figlewicz D.A., Szczudlik A. Cerebrovasc. Dis. 19:165-170(2005) · Mapped (4) |
| DD genotype of ACE gene is a risk factor for intracerebral hemorrhage. Slowik A., Turaj W., Dziedzic T., Haefele A., Pera J., Malecki M.T., Glodzik-Sobanska L., Szermer P., Figlewicz D.A., Szczudlik A. Neurology 63:359-361(2004) · UniProtKB (1) |
| A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males. Slowik A., Dziedzic T., Turaj W., Pera J., Glodzik-Sobanska L., Szermer P., Malecki M.T., Figlewicz D.A., Szczudlik A. Stroke 35:1589-1593(2004) · Mapped (5) |

