PubMed

Carney complex (CNC).

Bertherat J.

Orphanet J Rare Dis. 2006 Jun 6;1:21. Review.PMID: 16756677 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Adrenal pathophysiology: lessons from the Carney complex.

Groussin L, Cazabat L, René-Corail F, Jullian E, Bertherat J.

Horm Res. 2005;64(3):132-9. Epub 2005 Sep 27. Review.PMID: 16192737 [PubMed - indexed for MEDLINE]Related citations

PRKAR1A mutations in primary pigmented nodular adrenocortical disease.

Cazabat L, Ragazzon B, Groussin L, Bertherat J.

Pituitary. 2006;9(3):211-9. Review.PMID: 17036196 [PubMed - indexed for MEDLINE]Related citations

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. Review.PMID: 12119264 [PubMed - indexed for MEDLINE]Related citations

Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes.

Bertherat J, Horvath A, Groussin L, Grabar S, Boikos S, Cazabat L, Libe R, René-Corail F, Stergiopoulos S, Bourdeau I, Bei T, Clauser E, Calender A, Kirschner LS, Bertagna X, Carney JA, Stratakis CA.

J Clin Endocrinol Metab. 2009 Jun;94(6):2085-91. Epub 2009 Mar 17.PMID: 19293268 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease.

Groussin L, Jullian E, Perlemoine K, Louvel A, Leheup B, Luton JP, Bertagna X, Bertherat J.

J Clin Endocrinol Metab. 2002 Sep;87(9):4324-9.PMID: 12213893 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

Clinical and molecular genetics of primary pigmented nodular adrenocortical disease.

Sandrini F, Stratakis C.

Arq Bras Endocrinol Metabol. 2004 Oct;48(5):637-41. Epub 2005 Mar 7. Review.PMID: 15761532 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

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 [PubMed - indexed for MEDLINE]Related citations

Carney Complex.

Stratakis CA, Horvath A

In: Pagon RA, Bird TC, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-.
2003 Feb 5 [updated 2010 Jun 22].PMID: 20301463 [PubMed]Books & DocumentsFree textRelated citations

Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.

Pereira AM, Hes FJ, Horvath A, Woortman S, Greene E, Bimpaki E, Alatsatianos A, Boikos S, Smit JW, Romijn JA, Nesterova M, Stratakis CA.

J Clin Endocrinol Metab. 2010 Jan;95(1):338-42. Epub 2009 Nov 13.PMID: 19915019 [PubMed - indexed for MEDLINE]Related citations

Protein kinase A and its role in human neoplasia: the Carney complex paradigm.

Bossis I, Voutetakis A, Bei T, Sandrini F, Griffin KJ, Stratakis CA.

Endocr Relat Cancer. 2004 Jun;11(2):265-80. Review.PMID: 15163302 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!

Stergiopoulos SG, Stratakis CA.

FEBS Lett. 2003 Jul 3;546(1):59-64. Review.PMID: 12829237 [PubMed - indexed for MEDLINE]Related citations

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.

Groussin L, Horvath A, Jullian E, Boikos S, Rene-Corail F, Lefebvre H, Cephise-Velayoudom FL, Vantyghem MC, Chanson P, Conte-Devolx B, Lucas M, Gentil A, Malchoff CD, Tissier F, Carney JA, Bertagna X, Stratakis CA, Bertherat J.

J Clin Endocrinol Metab. 2006 May;91(5):1943-9. Epub 2006 Feb 7.PMID: 16464939 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

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 [PubMed - indexed for MEDLINE]Related citations

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. Epub 2008 Sep 19.PMID: 18804312 [PubMed - indexed for MEDLINE]Related citations

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 [PubMed - indexed for MEDLINE]Related citations

[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 [PubMed - indexed for MEDLINE]Related citations

Detection of somatic beta-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD).

Tadjine M, Lampron A, Ouadi L, Horvath A, Stratakis CA, Bourdeau I.

Clin Endocrinol (Oxf). 2008 Sep;69(3):367-73. Epub 2008 Apr 14.PMID: 18419788 [PubMed - indexed for MEDLINE]Related citations

Genetic analysis in a patient with recurrent cardiac myxoma and endocrinopathy.

Imai Y, Taketani T, Maemura K, Takeda N, Harada T, Nojiri T, Kawanami D, Monzen K, Hayashi D, Murakawa Y, Ohno M, Hirata Y, Yamazaki T, Takamoto S, Nagai R.

Circ J. 2005 Aug;69(8):994-5.PMID: 16041174 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

Carney complex: the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas.

Carney JA.

Semin Dermatol. 1995 Jun;14(2):90-8.PMID: 7640202 [PubMed - indexed for MEDLINE]Related citations