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Journal Abstract Search

223 related items for PubMed ID: 11744997

  • 21. Inherited disposition to cardiac myxoma development.
    Wilkes D, Charitakis K, Basson CT.
    Nat Rev Cancer; 2006 Feb; 6(2):157-65. PubMed ID: 16491075
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  • 22. Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.
    Casey M, Vaughan CJ, He J, Hatcher CJ, Winter JM, Weremowicz S, Montgomery K, Kucherlapati R, Morton CC, Basson CT.
    J Clin Invest; 2000 Sep; 106(5):R31-8. PubMed ID: 10974026
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  • 23. [Carney's Complex: familial cardiac myxoma].
    Guerra MS, Santos N, Neves F, Carlos Mota J, Miranda JA, Vouga L.
    Rev Port Cir Cardiotorac Vasc; 2006 Sep; 13(2):79-81. PubMed ID: 16862261
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  • 24. Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex).
    Basson CT, MacRae CA, Korf B, Merliss A.
    Am J Cardiol; 1997 Apr 01; 79(7):994-5. PubMed ID: 9104925
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  • 25. Heterogeneity of skin manifestations in patients with Carney complex.
    Mateus C, Palangié A, Franck N, Groussin L, Bertagna X, Avril MF, Bertherat J, Dupin N.
    J Am Acad Dermatol; 2008 Nov 01; 59(5):801-10. PubMed ID: 18804312
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  • 27. Appraisal of histogenesis of cardiac myxoma: our experience of 78 cases and review of literature.
    Chopra P, Ray R, Airan B, Talwar KK, Venugopal P.
    Indian Heart J; 1999 Nov 01; 51(1):69-74. PubMed ID: 10327783
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  • 28. The Carney complex (myxomas, spotty pigmentation, endocrine overactivity, and schwannomas).
    Carney JA.
    Dermatol Clin; 1995 Jan 01; 13(1):19-26. PubMed ID: 7712644
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  • 29. Clinical phenotypes and molecular genetic mechanisms of Carney complex.
    Wilkes D, McDermott DA, Basson CT.
    Lancet Oncol; 2005 Jul 01; 6(7):501-8. PubMed ID: 15992699
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  • 33. Syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).
    Legius E, Daenen W, Vandenbergh V, Verbeeck G, Bex M, Fryns JP.
    Genet Couns; 1998 Jul 01; 9(4):287-90. PubMed ID: 9894167
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  • 38. [Association of cardiac myxomas and pigmented cutaneous lesions: a new cardiocutaneous syndrome?].
    Ortonne JP.
    Ann Dermatol Venereol; 1986 Jul 01; 113(12):1279-81. PubMed ID: 3566075
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  • 40. Analysis of GNAS1 and PRKAR1A gene mutations in human cardiac myxomas not associated with multiple endocrine disorders.
    Mantovani G, Bondioni S, Corbetta S, Menicanti L, Rubino B, Peverelli E, Labarile P, Dall'Asta C, Ambrosi B, Beck-Peccoz P, Lania AG, Spada A.
    J Endocrinol Invest; 2009 Jun 01; 32(6):501-4. PubMed ID: 19494712
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