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Journal Abstract Search

326 related items for PubMed ID: 26096872

  • 1. Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome in a boy with Loeys-Dietz syndrome.
    Akazawa Y, Inaba Y, Hachiya A, Motoki N, Matsuzaki S, Minatoya K, Morisaki T, Morisaki H, Kosaki K, Kosho T, Koike K.
    Am J Med Genet A; 2015 Oct; 167A(10):2435-9. PubMed ID: 26096872
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  • 3. Systemic vascular phenotypes of Loeys-Dietz syndrome in a child carrying a de novo R381P mutation in TGFBR2: a case report.
    Uike K, Matsushita Y, Sakai Y, Togao O, Nagao M, Ishizaki Y, Nagata H, Yamamura K, Torisu H, Hara T.
    BMC Res Notes; 2013 Nov 12; 6():456. PubMed ID: 24220024
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  • 6. Novel pathogenic TGFBR1 and SMAD3 variants identified after cerebrovascular events in adult patients with Loeys-dietz syndrome.
    Laterza D, Ritelli M, Zini A, Colombi M, Dell'Acqua ML, Vandelli L, Bigliardi G, Verganti L, Vallone S, Vincenzi C, Rosafio F, Ciolli L, Calabrese O, Nichelli PF, Picchetto L.
    Eur J Med Genet; 2019 Oct 12; 62(10):103727. PubMed ID: 31326520
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  • 9. 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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  • 10. Progressive aortic root and pulmonary artery aneurysms in a neonate with Loeys-Dietz syndrome type 1B.
    Muramatsu Y, Kosho T, Magota M, Yokotsuka T, Ito M, Yasuda A, Kito O, Suzuki C, Nagata Y, Kawai S, Ikoma M, Hatano T, Nakayama M, Kawamura R, Wakui K, Morisaki H, Morisaki T, Fukushima Y.
    Am J Med Genet A; 2010 Feb 26; 152A(2):417-21. PubMed ID: 20101701
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  • 12. Heterogeneity of aortic disease severity in patients with Loeys-Dietz syndrome.
    Teixidó-Tura G, Franken R, Galuppo V, Gutiérrez García-Moreno L, Borregan M, Mulder BJ, García-Dorado D, Evangelista A.
    Heart; 2016 Apr 26; 102(8):626-32. PubMed ID: 26848186
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  • 14. Germline TGF-beta receptor mutations and skeletal fragility: a report on two patients with Loeys-Dietz syndrome.
    Kirmani S, Tebben PJ, Lteif AN, Gordon D, Clarke BL, Hefferan TE, Yaszemski MJ, McGrann PS, Lindor NM, Ellison JW.
    Am J Med Genet A; 2010 Apr 26; 152A(4):1016-9. PubMed ID: 20358619
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  • 17. Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesis.
    Gallo EM, Loch DC, Habashi JP, Calderon JF, Chen Y, Bedja D, van Erp C, Gerber EE, Parker SJ, Sauls K, Judge DP, Cooke SK, Lindsay ME, Rouf R, Myers L, ap Rhys CM, Kent KC, Norris RA, Huso DL, Dietz HC.
    J Clin Invest; 2014 Jan 26; 124(1):448-60. PubMed ID: 24355923
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  • 19. Overexpression of Gremlin-1 in patients with Loeys-Dietz syndrome: implications on pathophysiology and early disease detection.
    Wellbrock J, Sheikhzadeh S, Oliveira-Ferrer L, Stamm H, Hillebrand M, Keyser B, Klokow M, Vohwinkel G, Bonk V, Otto B, Streichert T, Balabanov S, Hagel C, Rybczynski M, Bentzien F, Bokemeyer C, von Kodolitsch Y, Fiedler W.
    PLoS One; 2014 Jan 26; 9(8):e104742. PubMed ID: 25116393
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  • 20. A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation.
    Tug E, Loeys B, De Paepe A, Aydin H, Gideroglu K.
    Genet Couns; 2010 Jan 26; 21(2):225-32. PubMed ID: 20681224
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