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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 2 |
2011 | 1 |
2013 | 2 |
2015 | 1 |
2024 | 0 |
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Page 1
Rare Coding Variation and Risk of Intracerebral Hemorrhage.
Stroke. 2015 Aug;46(8):2299-301. doi: 10.1161/STROKEAHA.115.009838. Epub 2015 Jun 25.
Stroke. 2015.
PMID: 26111891
Free PMC article.
APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study.
Biffi A, Anderson CD, Jagiella JM, Schmidt H, Kissela B, Hansen BM, Jimenez-Conde J, Pires CR, Ayres AM, Schwab K, Cortellini L, Pera J, Urbanik A, Romero JM, Rost NS, Goldstein JN, Viswanathan A, Pichler A, Enzinger C, Rabionet R, Norrving B, Tirschwell DL, Selim M, Brown DL, Silliman SL, Worrall BB, Meschia JF, Kidwell CS, Broderick JP, Greenberg SM, Roquer J, Lindgren A, Slowik A, Schmidt R, Woo D, Rosand J; International Stroke Genetics Consortium.
Biffi A, et al.
Lancet Neurol. 2011 Aug;10(8):702-9. doi: 10.1016/S1474-4422(11)70148-X. Epub 2011 Jul 6.
Lancet Neurol. 2011.
PMID: 21741316
Free PMC article.
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Risk of thromboembolism following acute intracerebral hemorrhage.
Goldstein JN, Fazen LE, Wendell L, Chang Y, Rost NS, Snider R, Schwab K, Chanderraj R, Kabrhel C, Kinnecom C, Fitzmaurice E, Smith EE, Greenberg SM, Rosand J.
Goldstein JN, et al.
Neurocrit Care. 2009;10(1):28-34. doi: 10.1007/s12028-008-9134-3. Epub 2008 Sep 23.
Neurocrit Care. 2009.
PMID: 18810667
Free PMC article.
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Screening for familial APP mutations in sporadic cerebral amyloid angiopathy.
Biffi A, Plourde A, Shen Y, Onofrio R, Smith EE, Frosch M, Prada CM, Gusella J, Greenberg SM, Rosand J.
Biffi A, et al.
PLoS One. 2010 Nov 11;5(11):e13949. doi: 10.1371/journal.pone.0013949.
PLoS One. 2010.
PMID: 21085603
Free PMC article.
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Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage.
Anderson CD, Biffi A, Nalls MA, Devan WJ, Schwab K, Ayres AM, Valant V, Ross OA, Rost NS, Saxena R, Viswanathan A, Worrall BB, Brott TG, Goldstein JN, Brown D, Broderick JP, Norrving B, Greenberg SM, Silliman SL, Hansen BM, Tirschwell DL, Lindgren A, Slowik A, Schmidt R, Selim M, Roquer J, Montaner J, Singleton AB, Kidwell CS, Woo D, Furie KL, Meschia JF, Rosand J; International Stroke Genetics Consortium.
Anderson CD, et al.
Stroke. 2013 Mar;44(3):612-9. doi: 10.1161/STROKEAHA.112.672089. Epub 2013 Jan 29.
Stroke. 2013.
PMID: 23362085
Free PMC article.
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Variants at APOE influence risk of deep and lobar intracerebral hemorrhage.
Biffi A, Sonni A, Anderson CD, Kissela B, Jagiella JM, Schmidt H, Jimenez-Conde J, Hansen BM, Fernandez-Cadenas I, Cortellini L, Ayres A, Schwab K, Juchniewicz K, Urbanik A, Rost NS, Viswanathan A, Seifert-Held T, Stoegerer EM, Tomás M, Rabionet R, Estivill X, Brown DL, Silliman SL, Selim M, Worrall BB, Meschia JF, Montaner J, Lindgren A, Roquer J, Schmidt R, Greenberg SM, Slowik A, Broderick JP, Woo D, Rosand J; International Stroke Genetics Consortium.
Biffi A, et al.
Ann Neurol. 2010 Dec;68(6):934-43. doi: 10.1002/ana.22134.
Ann Neurol. 2010.
PMID: 21061402
Free PMC article.
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Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes.
Meschia JF, Arnett DK, Ay H, Brown RD Jr, Benavente OR, Cole JW, de Bakker PI, Dichgans M, Doheny KF, Fornage M, Grewal RP, Gwinn K, Jern C, Conde JJ, Johnson JA, Jood K, Laurie CC, Lee JM, Lindgren A, Markus HS, McArdle PF, McClure LA, Mitchell BD, Schmidt R, Rexrode KM, Rich SS, Rosand J, Rothwell PM, Rundek T, Sacco RL, Sharma P, Shuldiner AR, Slowik A, Wassertheil-Smoller S, Sudlow C, Thijs VN, Woo D, Worrall BB, Wu O, Kittner SJ; NINDS SiGN Study.
Meschia JF, et al.
Stroke. 2013 Oct;44(10):2694-702. doi: 10.1161/STROKEAHA.113.001857. Epub 2013 Sep 10.
Stroke. 2013.
PMID: 24021684
Free PMC article.
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