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Items: 1 to 20 of 79

1.

Spectrum of malignancy and premalignancy in Carney syndrome.

Nwokoro NA, Korytkowski MT, Rose S, Gorin MB, Penles Stadler M, Witchel SF, Mulvihill JJ.

Am J Med Genet. 1997 Dec 31;73(4):369-77.

PMID:
9415461
2.

Carney complex: report of a kindred with predominantly cutaneous manifestations.

Armstrong DK, Irvine AD, Handley JM, Walsh MY, Hadden DR, Bingham EA.

Br J Dermatol. 1997 Apr;136(4):578-82.

PMID:
9155962
3.

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
4.

[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
5.

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
6.
7.

[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
8.

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;59(5):801-10. doi: 10.1016/j.jaad.2008.07.032. Epub 2008 Sep 19.

PMID:
18804312
9.

Genetic mutations in thyroid carcinoma.

Taccaliti A, Boscaro M.

Minerva Endocrinol. 2009 Mar;34(1):11-28. Review.

PMID:
19209125
10.

Melanotic nonpsammomatous trigeminal schwannoma as the first manifestation of Carney complex: case report.

Carrasco CA, Rojas-Salazar D, Chiorino R, Venega JC, Wohllk N.

Neurosurgery. 2006 Dec;59(6):E1334-5; discussion E1335.

PMID:
17277668
11.

Carney complex.

Zahedi RG, Wald DS, Ohri S.

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

PMID:
16798242
12.

Familial thyroid carcinoma: a diagnostic algorithm.

Dotto J, Nosé V.

Adv Anat Pathol. 2008 Nov;15(6):332-49. doi: 10.1097/PAP.0b013e31818a64af. Review.

PMID:
18948764
13.

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
14.

[Muir-Torre syndrome].

Körber J, Djawari D.

Hautarzt. 2001 Dec;52(12):1107-10. German.

PMID:
11910863
15.

["Myxoma syndrome"--a "benign" disease with "malignant" course].

Saurbier B, Giebel A, Gabelmann M, Konstantinides S, Kaser W, Spillner G, Schöllhorn J, Beyersdorf F, Just H.

Z Kardiol. 1997 Aug;86(8):592-7. German.

PMID:
9417749
16.

Rare syndromes.

Jabbour SA, Davidovici BB, Wolf R.

Clin Dermatol. 2006 Jul-Aug;24(4):299-316. Review.

PMID:
16828412
17.

Prolactin secretion abnormalities in patients with the "syndrome of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

Raff SB, Carney JA, Krugman D, Doppman JL, Stratakis CA.

J Pediatr Endocrinol Metab. 2000 Apr;13(4):373-9.

PMID:
10776991
18.

Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.

Zbuk KM, Patocs A, Shealy A, Sylvester H, Miesfeldt S, Eng C.

Nat Clin Pract Oncol. 2007 Oct;4(10):608-12.

PMID:
17898811
19.

Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.

Ponti G, Ponz de Leon M, Maffei S, Pedroni M, Losi L, Di Gregorio C, Gismondi V, Scarselli A, Benatti P, Roncari B, Seidenari S, Pellacani G, Varotti C, Prete E, Varesco L, Roncucci L.

Clin Genet. 2005 Nov;68(5):442-7.

PMID:
16207212
20.

Familial cardiac myxoma--a comprehensive review of reported cases.

Singh SD, Lansing AM.

J Ky Med Assoc. 1996 Mar;94(3):96-104. Review.

PMID:
8820573
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