Figlewicz DA - Search Results

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 MT, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Stroke. 2004 Jul;35(7):1589-93. doi: 10.1161/01.STR.0000132194.24663.3d. Epub 2004 Jun 3. Stroke. 2004. PMID: 15178823

2

II genotype of the angiotensin-converting enzyme gene increases the risk for subarachnoid hemorrhage from ruptured aneurysm.

Slowik A, Borratynska A, Pera J, Betlej M, Dziedzic T, Krzyszkowski T, Czepko R, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Stroke. 2004 Jul;35(7):1594-7. doi: 10.1161/01.STR.0000131655.45227.f7. Epub 2004 May 27. Stroke. 2004. PMID: 15166392

3

Coagulation factor XIII VaI34Leu polymorphism in patients with small vessel disease or primary intracerebral hemorrhage.

Slowik A, Dziedzic T, Pera J, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Cerebrovasc Dis. 2005;19(3):165-70. doi: 10.1159/000083251. Epub 2005 Jan 11. Cerebrovasc Dis. 2005. PMID: 15644629

4

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 DA, Betlej M, Krzyszkowski T, Czepko R, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Stroke. 2005 Apr;36(4):737-40. doi: 10.1161/01.STR.0000157598.02014.37. Epub 2005 Feb 17. Stroke. 2005. PMID: 15718509

5

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, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Cerebrovasc Dis. 2007;23(5-6):395-400. doi: 10.1159/000101462. Epub 2007 Apr 2. Cerebrovasc Dis. 2007. PMID: 17406108

6

DD genotype of ACE gene is a risk factor for intracerebral hemorrhage.

Slowik A, Turaj W, Dziedzic T, Haefele A, Pera J, Malecki MT, Glodzik-Sobanska L, Szermer P, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Neurology. 2004 Jul 27;63(2):359-61. doi: 10.1212/01.wnl.0000130200.12993.0c. Neurology. 2004. PMID: 15277638

7

Paraoxonase gene polymorphisms and sporadic ALS.

Slowik A, Tomik B, Wolkow PP, Partyka D, Turaj W, Malecki MT, Pera J, Dziedzic T, Szczudlik A, Figlewicz DA. Slowik A, et al. Among authors: figlewicz da. Neurology. 2006 Sep 12;67(5):766-70. doi: 10.1212/01.wnl.0000219565.32247.11. Epub 2006 Jul 5. Neurology. 2006. PMID: 16822965

8

Lack of association between VEGF gene polymorphisms and plasma VEGF levels and sporadic AL.

Golenia A, Tomik B, Zawislak D, Wolkow P, Dziubek A, Sado M, Szczudlik A, Figlewicz DA, Slowik A. Golenia A, et al. Among authors: figlewicz da. Neurology. 2010 Nov 30;75(22):2035-7. doi: 10.1212/WNL.0b013e3181ff9658. Neurology. 2010. PMID: 21115961 No abstract available.

9

Paraoxonase-1 Q192R polymorphism and risk of sporadic amyotrophic lateral sclerosis.

Slowik A, Tomik B, Partyka D, Turaj W, Pera J, Dziedzic T, Szermer P, Figlewicz DA, Szczudlik A. Slowik A, et al. Among authors: figlewicz da. Clin Genet. 2006 Apr;69(4):358-9. doi: 10.1111/j.1399-0004.2006.00590.x. Clin Genet. 2006. PMID: 16630171 Free article. No abstract available.

10

A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy.

Tomik B, Partyka D, Sułek A, Kurek-Gryz EA, Banach M, Ostrowska M, Zaremba J, Figlewicz DA, Szczudlik A. Tomik B, et al. Among authors: figlewicz da. Amyotroph Lateral Scler. 2006 Jun;7(2):72-9. doi: 10.1080/17482960600664839. Amyotroph Lateral Scler. 2006. PMID: 16753970

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