152 related articles for article (PubMed ID: 22020668)
1. A novel PRKAR1A mutation in Korean Carney complex family.
Rhee SY; Kwon HS; Lee JH; Woo JT; Kim MK; Lim YJ; Rhee BA; Koh SH; Lee S; Lee MH; Kim DY; Chon S; Oh S; Kim SW; Kim JW; Kim YS; Choi YK
Exp Clin Endocrinol Diabetes; 2012 Jan; 120(1):7-13. PubMed ID: 22020668
[TBL] [Abstract][Full Text] [Related]
2. A Novel Inherited Mutation in PRKAR1A Abrogates PreRNA Splicing in a Carney Complex Family.
Sun Y; Chen X; Sun J; Wen X; Liu X; Zhang Y; Hoffman AR; Hu JF; Gao Y
Can J Cardiol; 2015 Nov; 31(11):1393-401. PubMed ID: 26416542
[TBL] [Abstract][Full Text] [Related]
3. 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]
4.
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]
5. 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]
6. 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]
7. 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]
8. Identification of a novel mutation of the PRKAR1A gene in a patient with Carney complex with significant osteoporosis and recurrent fractures.
Papanastasiou L; Fountoulakis S; Voulgaris N; Kounadi T; Choreftaki T; Kostopoulou A; Zografos G; Lyssikatos C; Stratakis CA; Piaditis G
Hormones (Athens); 2016; 15(1):129-35. PubMed ID: 27377598
[TBL] [Abstract][Full Text] [Related]
9. Case studies of two related Chinese patients with Carney complex presenting with extensive cardiac myxomas and PRKAR1A gene mutation of c.491_492delTG.
Guo H; Xu J; Xiong H; Hu S
World J Surg Oncol; 2015 Feb; 13():83. PubMed ID: 25890363
[TBL] [Abstract][Full Text] [Related]
10. Germline deletion and a somatic mutation of the PRKAR1A gene in a Carney complex-related pituitary adenoma.
Iwata T; Tamanaha T; Koezuka R; Tochiya M; Makino H; Kishimoto I; Mizusawa N; Ono S; Inoshita N; Yamada S; Shimatsu A; Yoshimoto K
Eur J Endocrinol; 2015 Jan; 172(1):K5-10. PubMed ID: 25336503
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. A Novel Missense PRKAR1A Variant Causes Carney Complex.
Kim B; Jang HN; Chae KS; Shin HS; Kim YH; Kim SJ; Seong MW; Kim JH
Endocrinol Metab (Seoul); 2022 Oct; 37(5):810-815. PubMed ID: 36193716
[TBL] [Abstract][Full Text] [Related]
14. In vitro studies of novel PRKAR1A mutants that extend the predicted RIα protein sequence into the 3'-untranslated open reading frame: proteasomal degradation leads to RIα haploinsufficiency and Carney complex.
Patronas Y; Horvath A; Greene E; Tsang K; Bimpaki E; Haran M; Nesterova M; Stratakis CA
J Clin Endocrinol Metab; 2012 Mar; 97(3):E496-502. PubMed ID: 22205709
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations.
Gennari M; Stratakis CA; Hovarth A; Pirazzoli P; Cicognani A
Clin Endocrinol (Oxf); 2008 Nov; 69(5):751-5. PubMed ID: 18445140
[TBL] [Abstract][Full Text] [Related]
18. Sporadic Carney complex without PRKAR1A mutation in a young patient with ischemic stroke.
Aguiar de Sousa D; Gouveia AI; Wessling A; Geraldes R; Canhão P
J Stroke Cerebrovasc Dis; 2015 Mar; 24(3):e79-81. PubMed ID: 25576349
[TBL] [Abstract][Full Text] [Related]
19. A Novel Mutation of
Cai XL; Wu J; Luo YY; Chen L; Han XY; Ji LN
Chin Med J (Engl); 2017 Dec; 130(24):3009-3010. PubMed ID: 29237939
[No Abstract] [Full Text] [Related]
20. [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]
[Next] [New Search]
