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The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.
Mata IF, Jang Y, Kim CH, Hanna DS, Dorschner MO, Samii A, Agarwal P, Roberts JW, Klepitskaya O, Shprecher DR, Chung KA, Factor SA, Espay AJ, Revilla FJ, Higgins DS, Litvan I, Leverenz JB, Yearout D, Inca-Martinez M, Martinez E, Thompson TR, Cholerton BA, Hu SC, Edwards KL, Kim KS, Zabetian CP. Mata IF, et al. Among authors: thompson tr. Mol Neurodegener. 2015 Sep 24;10:50. doi: 10.1186/s13024-015-0045-4. Mol Neurodegener. 2015. PMID: 26399558 Free PMC article.
Implementation of critical congenital heart disease screening in Minnesota.
Kochilas LK, Lohr JL, Bruhn E, Borman-Shoap E, Gams BL, Pylipow M, Saarinen A, Gaviglio A, Thompson TR. Kochilas LK, et al. Among authors: thompson tr. Pediatrics. 2013 Sep;132(3):e587-94. doi: 10.1542/peds.2013-0803. Epub 2013 Aug 19. Pediatrics. 2013. PMID: 23958775
Prediction of arrhythmic events in ischemic and dilated cardiomyopathy patients referred for implantable cardiac defibrillator: evaluation of multiple scar quantification measures for late gadolinium enhancement magnetic resonance imaging.
Gao P, Yee R, Gula L, Krahn AD, Skanes A, Leong-Sit P, Klein GJ, Stirrat J, Fine N, Pallaveshi L, Wisenberg G, Thompson TR, Prato F, Drangova M, White JA. Gao P, et al. Among authors: thompson tr. Circ Cardiovasc Imaging. 2012 Jul;5(4):448-56. doi: 10.1161/CIRCIMAGING.111.971549. Epub 2012 May 9. Circ Cardiovasc Imaging. 2012. PMID: 22572740
109 results