518 related articles for article (PubMed ID: 26130139)
1. 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]
2. Carney complex review: Genetic features.
Bosco Schamun MB; Correa R; Graffigna P; de Miguel V; Fainstein Day P
Endocrinol Diabetes Nutr (Engl Ed); 2018 Jan; 65(1):52-59. PubMed ID: 29162369
[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].
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]
5.
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]
6. 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]
7. 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]
8. 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]
9. Phenotypic Variability in a Family with Carney Complex Accompanied by a Novel Mutation Involving PRKAR1A.
Kubo H; Tsurutani Y; Sugisawa C; Sunouchi T; Hirose R; Saito J
Tohoku J Exp Med; 2022 Jul; 257(4):337-345. PubMed ID: 35732416
[TBL] [Abstract][Full Text] [Related]
10. 17q22-24 chromosomal losses and alterations of protein kinase a subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia.
Bourdeau I; Matyakhina L; Stergiopoulos SG; Sandrini F; Boikos S; Stratakis CA
J Clin Endocrinol Metab; 2006 Sep; 91(9):3626-32. PubMed ID: 16772351
[TBL] [Abstract][Full Text] [Related]
11. Recurrent left atrial myxomas in Carney complex: a genetic cause of multiple strokes that can be prevented.
Briassoulis G; Kuburovic V; Xekouki P; Patronas N; Keil MF; Lyssikatos C; Stajevic M; Kovacevic G; Stratakis CA
J Stroke Cerebrovasc Dis; 2012 Nov; 21(8):914.e1-8. PubMed ID: 22341669
[TBL] [Abstract][Full Text] [Related]
12. Frequent protein kinase A regulatory subunit A1 mutations but no GNAS mutations as potential driver in sporadic cardiac myxomas.
Zimpfer A; Abel LM; Alozie A; Etz CD; Schneider B
Cardiovasc Pathol; 2024; 71():107632. PubMed ID: 38492686
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Carney complex with PRKAR1A gene mutation: A case report and literature review.
Liu Q; Tong D; Liu G; Yi Y; Zhang D; Zhang J; Zhang Y; Huang Z; Li Y; Chen R; Guan Y; Yi X; Jiang J
Medicine (Baltimore); 2017 Dec; 96(50):e8999. PubMed ID: 29390296
[TBL] [Abstract][Full Text] [Related]
16. Novel PRKAR1A gene mutations in Carney Complex.
Pan L; Peng L; Jean-Gilles J; Zhang X; Wieczorek R; Jain S; Levine V; Osman I; Prieto VG; Lee P
Int J Clin Exp Pathol; 2010 May; 3(5):545-8. PubMed ID: 20606737
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Fibrolamellar carcinoma in the Carney complex: PRKAR1A loss instead of the classic DNAJB1-PRKACA fusion.
Graham RP; Lackner C; Terracciano L; González-Cantú Y; Maleszewski JJ; Greipp PT; Simon SM; Torbenson MS
Hepatology; 2018 Oct; 68(4):1441-1447. PubMed ID: 29222914
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel mutation in
Ghazi AA; Mandegar MH; Abazari M; Behzadnia N; Sadeghian T; Torbaghan SS; Amirbaigloo A
Arch Endocrinol Metab; 2021 Nov; 65(3):376-380. PubMed ID: 33939912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
