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Journal Abstract Search

626 related items for PubMed ID: 26333736

  • 1. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.
    Haller G, Alvarado DM, Willing MC, Braverman AC, Bridwell KH, Kelly M, Lenke LG, Luhmann SJ, Gurnett CA, Dobbs MB.
    J Bone Joint Surg Am; 2015 Sep 02; 97(17):1411-7. PubMed ID: 26333736
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  • 3. Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome.
    De Cario R, Sticchi E, Lucarini L, Attanasio M, Nistri S, Marcucci R, Pepe G, Giusti B.
    J Vasc Surg; 2018 Jul 02; 68(1):225-233.e5. PubMed ID: 28847661
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  • 4. Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections.
    Cao Y, Tan H, Li Z, Linpeng S, Long X, Liang D, Wu L.
    Int Heart J; 2018 Sep 26; 59(5):1059-1068. PubMed ID: 30101859
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  • 9. Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2.
    Sheikhzadeh S, Rybczynski M, Habermann CR, Bernhardt AM, Arslan-Kirchner M, Keyser B, Kaemmerer H, Mir TS, Staebler A, Oezdal N, Robinson PN, Berger J, Meinertz T, von Kodolitsch Y.
    Clin Genet; 2011 Jun 26; 79(6):568-74. PubMed ID: 20662850
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  • 10. Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study.
    Zhang L, Gao LG, Zhang M, Zhou XL.
    Mol Vis; 2012 Jun 26; 18():55-63. PubMed ID: 22259224
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  • 11. Phenotypic heterogeneity of Marfan-like connective tissue disorders associated with mutations in the transforming growth factor-beta receptor genes.
    Akutsu K, Morisaki H, Takeshita S, Sakamoto S, Tamori Y, Yoshimuta T, Yokoyama N, Nonogi H, Ogino H, Morisaki T.
    Circ J; 2007 Aug 26; 71(8):1305-9. PubMed ID: 17652900
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  • 12. TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.
    Singh KK, Rommel K, Mishra A, Karck M, Haverich A, Schmidtke J, Arslan-Kirchner M.
    Hum Mutat; 2006 Aug 26; 27(8):770-7. PubMed ID: 16799921
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  • 13. Detection of 15 novel mutations in 52 children from 40 families with the Marfan or Loeys-Dietz syndrome and phenotype-genotype correlations.
    Pees C, Michel-Behnke I, Hagl M, Laccone F.
    Clin Genet; 2014 Dec 26; 86(6):552-7. PubMed ID: 24199744
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  • 14. Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?
    Waldmüller S, Müller M, Warnecke H, Rees W, Schöls W, Walterbusch G, Ennker J, Scheffold T.
    Eur J Cardiothorac Surg; 2007 Jun 26; 31(6):970-5. PubMed ID: 17418587
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  • 15. 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.
    N Engl J Med; 2006 Aug 24; 355(8):788-98. PubMed ID: 16928994
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  • 17. Loeys-Dietz syndrome.
    Van Laer L, Dietz H, Loeys B.
    Adv Exp Med Biol; 2014 Aug 24; 802():95-105. PubMed ID: 24443023
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  • 19. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis.
    Buchan JG, Alvarado DM, Haller GE, Cruchaga C, Harms MB, Zhang T, Willing MC, Grange DK, Braverman AC, Miller NH, Morcuende JA, Tang NL, Lam TP, Ng BK, Cheng JC, Dobbs MB, Gurnett CA.
    Hum Mol Genet; 2014 Oct 01; 23(19):5271-82. PubMed ID: 24833718
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  • 20. Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.
    Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N.
    Am J Med Genet A; 2006 Aug 15; 140(16):1719-25. PubMed ID: 16835936
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