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Journal Abstract Search

232 related items for PubMed ID: 20101701

  • 1. 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; 152A(2):417-21. PubMed ID: 20101701
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  • 3. Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.
    Drera B, Ritelli M, Zoppi N, Wischmeijer A, Gnoli M, Fattori R, Calzavara-Pinton PG, Barlati S, Colombi M.
    Orphanet J Rare Dis; 2009 Nov 02; 4():24. PubMed ID: 19883511
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Loeys BL, Dietz HC.
    ; 1993 Nov 02. PubMed ID: 20301312
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  • 6. 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 02; 167A(10):2435-9. PubMed ID: 26096872
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  • 7. Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome.
    Breckpot J, Budts W, De Zegher F, Vermeesch JR, Devriendt K.
    Eur J Med Genet; 2010 Oct 02; 53(6):408-10. PubMed ID: 20813212
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  • 8. Proximal paraparesis due to aortic dissection extending into bilateral carotid arteries in a patient with Loeys-Dietz syndrome.
    Goshgarian C, Lugo A, Salazar R.
    J Clin Neurosci; 2013 Dec 02; 20(12):1790-2. PubMed ID: 23591182
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  • 9. 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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  • 11. 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 24; 152A(4):1016-9. PubMed ID: 20358619
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  • 17. Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
    Arslan-Kirchner M, Epplen JT, Faivre L, Jondeau G, Schmidtke J, De Paepe A, Loeys B.
    Eur J Hum Genet; 2011 Oct 24; 19(10):. PubMed ID: 21522183
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  • 18. Familial aortic aneurysm and dissection due to transforming growth factor-beta receptor 2 mutation.
    Edelman JJ, Ramponi F, Bannon PG, Jeremy R.
    Interact Cardiovasc Thorac Surg; 2011 May 24; 12(5):863-5. PubMed ID: 21324918
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