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Year | Number of Results |
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2024 | 0 |
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Page 1
Causes and histopathology of ascending aortic disease in children and young adults.
Cardiovasc Pathol. 2011 Jan-Feb;20(1):15-25. doi: 10.1016/j.carpath.2009.09.008.
Cardiovasc Pathol. 2011.
PMID: 19926309
Free PMC article.
Review.
Musculoskeletal findings of Loeys-Dietz syndrome.
Erkula G, Sponseller PD, Paulsen LC, Oswald GL, Loeys BL, Dietz HC.
Erkula G, et al. Among authors: oswald gl.
J Bone Joint Surg Am. 2010 Aug 4;92(9):1876-83. doi: 10.2106/JBJS.I.01140.
J Bone Joint Surg Am. 2010.
PMID: 20686062
Item in Clipboard
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC.
Loeys BL, et al. Among authors: oswald gl.
N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695.
N Engl J Med. 2006.
PMID: 16928994
Free article.
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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
Sobreira NL, Cirulli ET, Avramopoulos D, Wohler E, Oswald GL, Stevens EL, Ge D, Shianna KV, Smith JP, Maia JM, Gumbs CE, Pevsner J, Thomas G, Valle D, Hoover-Fong JE, Goldstein DB.
Sobreira NL, et al. Among authors: oswald gl.
PLoS Genet. 2010 Jun 17;6(6):e1000991. doi: 10.1371/journal.pgen.1000991.
PLoS Genet. 2010.
PMID: 20577567
Free PMC article.
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Increased fracture risk and low bone mineral density in patients with loeys-dietz syndrome.
Tan EW, Offoha RU, Oswald GL, Skolasky RL, Dewan AK, Zhen G, Shapiro JR, Dietz HC, Cao X, Sponseller PD.
Tan EW, et al. Among authors: oswald gl.
Am J Med Genet A. 2013 Aug;161A(8):1910-4. doi: 10.1002/ajmg.a.36029. Epub 2013 Jul 4.
Am J Med Genet A. 2013.
PMID: 23825031
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Being the genuine me.
Oswald GL.
Oswald GL.
J Genet Couns. 2012 Apr;21(2):220-1. doi: 10.1007/s10897-011-9446-x. Epub 2011 Nov 30.
J Genet Couns. 2012.
PMID: 22127475
No abstract available.
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Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene.
Peddy SB, Vricella LA, Crosson JE, Oswald GL, Cohn RD, Cameron DE, Valle D, Loeys BL.
Peddy SB, et al. Among authors: oswald gl.
Pediatrics. 2006 May;117(5):1830-3. doi: 10.1542/peds.2005-2301.
Pediatrics. 2006.
PMID: 16651346
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