These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Mutation of perinatal myosin heavy chain associated with a Carney complex variant. Veugelers M; Bressan M; McDermott DA; Weremowicz S; Morton CC; Mabry CC; Lefaivre JF; Zunamon A; Destree A; Chaudron JM; Basson CT N Engl J Med; 2004 Jul; 351(5):460-9. PubMed ID: 15282353 [TBL] [Abstract][Full Text] [Related]
7. Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. Stratakis CA; Carney JA; Lin JP; Papanicolaou DA; Karl M; Kastner DL; Pras E; Chrousos GP J Clin Invest; 1996 Feb; 97(3):699-705. PubMed ID: 8609225 [TBL] [Abstract][Full Text] [Related]
8. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit (PRKAR1A) in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas" (Carney complex). Stratakis CA Ann N Y Acad Sci; 2002 Jun; 968():3-21. PubMed ID: 12119264 [TBL] [Abstract][Full Text] [Related]
9. 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 [TBL] [Abstract][Full Text] [Related]
10. PRKAR1A gene mutation in patients with cardiac myxoma. Mabuchi T; Shimizu M; Ino H; Yamguchi M; Terai H; Fujino N; Nagata M; Sakata K; Inoue M; Yoneda T; Mabuchi H Int J Cardiol; 2005 Jul; 102(2):273-7. PubMed ID: 15982496 [TBL] [Abstract][Full Text] [Related]
12. The Carney complex (myxomas, spotty pigmentation, endocrine overactivity, and schwannomas). Carney JA Dermatol Clin; 1995 Jan; 13(1):19-26. PubMed ID: 7712644 [TBL] [Abstract][Full Text] [Related]
13. Genetic alterations of Carney complex are not present in sporadic cardiac myxomas. Fogt F; Zimmerman RL; Hartmann CJ; Brown CA; Narula N Int J Mol Med; 2002 Jan; 9(1):59-60. PubMed ID: 11744997 [TBL] [Abstract][Full Text] [Related]
14. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Kirschner LS; Carney JA; Pack SD; Taymans SE; Giatzakis C; Cho YS; Cho-Chung YS; Stratakis CA Nat Genet; 2000 Sep; 26(1):89-92. PubMed ID: 10973256 [TBL] [Abstract][Full Text] [Related]
16. Genetic testing of the family with a Carney-complex member leads to successful early removal of an asymptomatic atrial myxoma in the mother of the patient. Aspres N; Bleasel NR; Stapleton KM Australas J Dermatol; 2003 May; 44(2):121-2. PubMed ID: 12752185 [TBL] [Abstract][Full Text] [Related]
17. Familial Atrial Myxoma: Three Related Cases at an Australian Tertiary Institution. Schmidt C; Doi A; Ura M; Cole C; Mundy J Ann Thorac Cardiovasc Surg; 2017 Aug; 23(4):203-206. PubMed ID: 28367853 [TBL] [Abstract][Full Text] [Related]
18. Carney complex: A clinicopathologic study on a single family from several Canadian provinces. Lao A; Silva J; Chiu B; Sergi CM Cardiovasc Pathol; 2024; 69():107599. PubMed ID: 38072094 [TBL] [Abstract][Full Text] [Related]
19. Case studies of two related Chinese patients with Carney complex presenting with extensive cardiac myxomas and PRKAR1A gene mutation of c.491_492delTG. Guo H; Xu J; Xiong H; Hu S World J Surg Oncol; 2015 Feb; 13():83. PubMed ID: 25890363 [TBL] [Abstract][Full Text] [Related]
20. [PRKAR1A gene mutations in two patients with myxoma syndrome (Carney complex)]. Skamrov AV; Feoktistova ES; Khaspekov GL; KovalevskiÄ DA; Goriunova LE; Bibilashvili RSh; VinnitskiÄ LI; Sheremet'eva GF; Nechaenko MA Kardiologiia; 2003; 43(7):77-82. PubMed ID: 12891303 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]