247 related articles for article (PubMed ID: 33444222)
1. MANAGEMENT OF ENDOCRINE DISEASE: Carney complex: clinical and genetic update 20 years after the identification of the CNC1 (PRKAR1A) gene.
Bouys L; Bertherat J
Eur J Endocrinol; 2021 Mar; 184(3):R99-R109. PubMed ID: 33444222
[TBL] [Abstract][Full Text] [Related]
2. Carney complex: an update.
Correa R; Salpea P; Stratakis CA
Eur J Endocrinol; 2015 Oct; 173(4):M85-97. PubMed ID: 26130139
[TBL] [Abstract][Full Text] [Related]
3. Carney complex.
Espiard S; Bertherat J
Front Horm Res; 2013; 41():50-62. PubMed ID: 23652670
[TBL] [Abstract][Full Text] [Related]
4. Carney complex (CNC).
Bertherat J
Orphanet J Rare Dis; 2006 Jun; 1():21. PubMed ID: 16756677
[TBL] [Abstract][Full Text] [Related]
5. PRKAR1A mutations in primary pigmented nodular adrenocortical disease.
Cazabat L; Ragazzon B; Groussin L; Bertherat J
Pituitary; 2006; 9(3):211-9. PubMed ID: 17036196
[TBL] [Abstract][Full Text] [Related]
6. [Carney complex].
Losada Grande EJ; Al Kassam Martínez D; González Boillos M
Endocrinol Nutr; 2011; 58(6):308-14. PubMed ID: 21536508
[TBL] [Abstract][Full Text] [Related]
7. Carney complex: Clinical and genetic 2010 update.
Vezzosi D; Vignaux O; Dupin N; Bertherat J
Ann Endocrinol (Paris); 2010 Dec; 71(6):486-93. PubMed ID: 20850710
[TBL] [Abstract][Full Text] [Related]
8.
Kiefer FW; Winhofer Y; Iacovazzo D; Korbonits M; Wolfsberger S; Knosp E; Trautinger F; Höftberger R; Krebs M; Luger A; Gessl A
Eur J Endocrinol; 2017 Aug; 177(2):K7-K12. PubMed ID: 28522647
[TBL] [Abstract][Full Text] [Related]
9. Unusual presentations of Carney Complex in patient with a novel PRKAR1A mutation.
Akin S; Noyan S; Dagdelen S; Pasaoglu I; Kaynaroglu V; Askun MM; Bilen CY; Kiratli H; Baydar DE; Onder S; Sokmensuer C; Aytemir K; Erkin G; Kiratli PO; Alikasifoglu M; Erbas T
Neuro Endocrinol Lett; 2017 Aug; 38(4):248-254. PubMed ID: 28871709
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 16192737
[TBL] [Abstract][Full Text] [Related]
11. A large family with Carney complex caused by the S147G PRKAR1A mutation shows a unique spectrum of disease including adrenocortical cancer.
Anselmo J; Medeiros S; Carneiro V; Greene E; Levy I; Nesterova M; Lyssikatos C; Horvath A; Carney JA; Stratakis CA
J Clin Endocrinol Metab; 2012 Feb; 97(2):351-9. PubMed ID: 22112814
[TBL] [Abstract][Full Text] [Related]
12. Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up.
Espiard S; Vantyghem MC; Assié G; Cardot-Bauters C; Raverot G; Brucker-Davis F; Archambeaud-Mouveroux F; Lefebvre H; Nunes ML; Tabarin A; Lienhardt A; Chabre O; Houang M; Bottineau M; Stroër S; Groussin L; Guignat L; Cabanes L; Feydy A; Bonnet F; North MO; Dupin N; Grabar S; Duboc D; Bertherat J
J Clin Endocrinol Metab; 2020 Mar; 105(3):. PubMed ID: 31912137
[TBL] [Abstract][Full Text] [Related]
13. Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.
Libé R; Horvath A; Vezzosi D; Fratticci A; Coste J; Perlemoine K; Ragazzon B; Guillaud-Bataille M; Groussin L; Clauser E; Raffin-Sanson ML; Siegel J; Moran J; Drori-Herishanu L; Faucz FR; Lodish M; Nesterova M; Bertagna X; Bertherat J; Stratakis CA
J Clin Endocrinol Metab; 2011 Jan; 96(1):E208-14. PubMed ID: 21047926
[TBL] [Abstract][Full Text] [Related]
14. Familial isolated primary pigmented nodular adrenocortical disease associated with a novel low penetrance PRKAR1A gene splice site mutation.
Storr HL; Metherell LA; Dias R; Savage MO; Rasmussen AK; Clark AJ; Main KM
Horm Res Paediatr; 2010; 73(2):115-9. PubMed ID: 20190548
[TBL] [Abstract][Full Text] [Related]
15. An Unusual Presentation of Carney Complex.
Dağdeviren Çakır A; Turan H; Celkan T; Çomunoğlu N; Ercan O; Evliyaoğlu O
J Clin Res Pediatr Endocrinol; 2020 Mar; 12(1):117-121. PubMed ID: 31117334
[TBL] [Abstract][Full Text] [Related]
16. Acromegaly in Carney complex.
Cuny T; Mac TT; Romanet P; Dufour H; Morange I; Albarel F; Lagarde A; Castinetti F; Graillon T; North MO; Barlier A; Brue T
Pituitary; 2019 Oct; 22(5):456-466. PubMed ID: 31264077
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A novel splice site mutation of the PRKAR1A gene, C.440+5 G>C, in a Chinese family with Carney complex.
Fu J; Lai F; Chen Y; Wan X; Wei G; Li Y; Xiao H; Cao X
J Endocrinol Invest; 2018 Aug; 41(8):909-917. PubMed ID: 29318463
[TBL] [Abstract][Full Text] [Related]
19. Genetics of micronodular adrenal hyperplasia and Carney complex.
Tirosh A; Valdés N; Stratakis CA
Presse Med; 2018; 47(7-8 Pt 2):e127-e137. PubMed ID: 30093212
[TBL] [Abstract][Full Text] [Related]
20. Novel genetic mutation in the background of Carney complex.
Halászlaki C; Takács I; Butz H; Patócs A; Lakatos P
Pathol Oncol Res; 2012 Apr; 18(2):149-52. PubMed ID: 22297707
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]