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Items: 1 to 20 of 142

1.

Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex).

Basson CT, MacRae CA, Korf B, Merliss A.

Am J Cardiol. 1997 Apr 1;79(7):994-5.

PMID:
9104925
2.

Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).

Milunsky J, Huang XL, Baldwin CT, Farah MG, Milunsky A.

Cancer Genet Cytogenet. 1998 Oct 15;106(2):173-6.

PMID:
9797786
3.

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex.

Casey M, Mah C, Merliss AD, Kirschner LS, Taymans SE, Denio AE, Korf B, Irvine AD, Hughes A, Carney JA, Stratakis CA, Basson CT.

Circulation. 1998 Dec 8;98(23):2560-6.

4.

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 1;97(3):699-705.

5.

[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 Apr-Jun;13(2):79-81. Portuguese.

PMID:
16862261
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 29;351(5):460-9.

7.

Evidence for a second genetic locus in Carney complex.

Irvine AD, Armstrong DK, Bingham EA, Hadden DR, Nevin NC, Hughes AE.

Br J Dermatol. 1998 Oct;139(4):572-6.

PMID:
9892898
8.

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.

PMID:
11744997
9.

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 10;102(2):273-7.

PMID:
15982496
10.

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).

Stratakis CA, Jenkins RB, Pras E, Mitsiadis CS, Raff SB, Stalboerger PG, Tsigos C, Carney JA, Chrousos GP.

J Clin Endocrinol Metab. 1996 Oct;81(10):3607-14.

PMID:
8855810
11.

Familial Cushing's syndrome ("Carney complex")

[No authors listed]

N Engl J Med. 1990 May 17;322(20):1469-70. No abstract available.

PMID:
2330017
12.

Molecular genetic diagnosis of the familial myxoma syndrome (Carney complex).

Goldstein MM, Casey M, Carney JA, Basson CT.

Am J Med Genet. 1999 Sep 3;86(1):62-5.

PMID:
10440831
13.

[PRKAR1A gene mutations in two patients with myxoma syndrome (Carney complex)].

Skamrov AV, Feoktistova ES, Khaspekov GL, Kovalevskiĭ DA, Goriunova LE, Bibilashvili RSh, Vinnitskiĭ LI, Sheremet'eva GF, Nechaenko MA.

Kardiologiia. 2003;43(7):77-82. Russian.

PMID:
12891303
14.

[Ocular findings in Carney complex].

Chinchurreta-Capote A, Trueba A, Hernández FJ, Piñas P, López S, Tena ME, Aznarez N, Portillo E, Castillón L.

Arch Soc Esp Oftalmol. 2006 Dec;81(12):709-11. Spanish.

PMID:
17199165
15.

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. Erratum in: Australas J Dermatol. 2003 Nov;44(4):508.

PMID:
12752185
16.

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;9(4):287-90.

PMID:
9894167
17.
18.

Carney complex.

Zahedi RG, Wald DS, Ohri S.

Ann Thorac Surg. 2006 Jul;82(1):320-2.

PMID:
16798242
19.

[Primary pigmented nodular adrenocortical dysplasia (PPNAD) within the scope of Carney complex as the etiology of Cushing syndrome].

Koch CA, Bornstein SR, Chrousos GP, Stratakis CA.

Med Klin (Munich). 2000 Apr 15;95(4):224-30. German.

PMID:
10808306
20.

No cytogenetic evidence for involvement of gene(s) at 2p16 in sporadic cardiac myxomas: cytogenetic changes in ten sporadic cardiac myxomas.

Dijkhuizen T, de Jong B, Meuzelaar JJ, Molenaar WM, van den Berg E.

Cancer Genet Cytogenet. 2001 Apr 15;126(2):162-5.

PMID:
11376810
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