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Results: 1 to 20 of 213

Similar articles for PubMed (Select 8609225)

1.

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.

2.

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
3.

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
5.

Chromosome 2 (2p16) abnormalities in Carney complex tumours.

Matyakhina L, Pack S, Kirschner LS, Pak E, Mannan P, Jaikumar J, Taymans SE, Sandrini F, Carney JA, Stratakis CA.

J Med Genet. 2003 Apr;40(4):268-77.

6.

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
7.

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.

8.

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
9.

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.

10.

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

Stratakis CA, Kirschner LS, Taymans SE, Tomlinson IP, Marsh DJ, Torpy DJ, Giatzakis C, Eccles DM, Theaker J, Houlston RS, Blouin JL, Antonarakis SE, Basson CT, Eng C, Carney JA.

J Clin Endocrinol Metab. 1998 Aug;83(8):2972-6.

PMID:
9709978
11.

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
12.

Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.

Wassif WS, Farnebo F, Teh BT, Moniz CF, Li FY, Harrison JD, Peters TJ, Larsson C, Harris P.

Clin Endocrinol (Oxf). 1999 Feb;50(2):191-6.

PMID:
10396361
13.

Carney complex--an unexpected finding during puerperium.

Schulz S, Redlich A, Köppe I, Reschke K, Weise W.

Gynecol Obstet Invest. 2001;51(3):211-3.

PMID:
11306912
14.
15.

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.

PMID:
10973256
16.

Pathology and molecular genetics of the pituitary gland in patients with the 'complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas' (Carney complex).

Stratakis CA, Matyakhina L, Courkoutsakis N, Patronas N, Voutetakis A, Stergiopoulos S, Bossis I, Carney JA.

Front Horm Res. 2004;32:253-64. Review.

PMID:
15281351
17.

[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
18.
19.

Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs alpha gene.

DeMarco L, Stratakis CA, Boson WL, Jakbovitz O, Carson E, Andrade LM, Amaral VF, Rocha JL, Choursos GP, Nordenskjöld M, Friedman E.

Hum Genet. 1996 Aug;98(2):185-8.

PMID:
8698339
20.

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
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