232 related articles for article (PubMed ID: 25576349)
1. 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]
2. A novel PRKAR1A mutation resulting in a splicing variant in a case of Carney complex.
Jang YS; Moon SD; Kim JH; Lee IS; Lee JM; Kim HS
Korean J Intern Med; 2015 Sep; 30(5):730-4. PubMed ID: 26354069
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Novel PRKAR1A mutation in Carney complex with cardiac myxoma.
Kondo K; Harada M; Konomoto T; Hatanaka M; Nunoi H
Pediatr Int; 2017 Jul; 59(7):840-841. PubMed ID: 28745458
[No Abstract] [Full Text] [Related]
7. 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]
8. Obstruction of the tricuspid valve orifice by a huge right atrial myxoma associated with the Carney complex: a case report.
Affronti A; Di Bella I; Prontera P; Da Col U; Ramoni E; Donti E; Paris M; Ragni T
J Card Surg; 2010 Nov; 25(6):674-6. PubMed ID: 20880078
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [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]
12. Carney Syndrome Presented as a Pathological Spine Fracture in a 35-Year-Old Male.
Kiriakopoulos A; Linos D
Am J Case Rep; 2018 Nov; 19():1366-1369. PubMed ID: 30442879
[TBL] [Abstract][Full Text] [Related]
13. 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; 102(2):273-7. PubMed ID: 15982496
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Association of Carney Complex with an Intronic Splice Site Mutation in the PRKAR1A Gene.
Guo H; Xiong H; Li Z; Xu J; Zhang H; Chen X; Hu S
Horm Metab Res; 2016 Jun; 48(6):384-8. PubMed ID: 26788925
[TBL] [Abstract][Full Text] [Related]
16. Carney complex syndrome manifesting as cardioembolic stroke: a case report and review of the literature.
Chatzikonstantinou S; Kazis D; Giannakopoulou P; Poulios P; Pikou O; Geroukis T; Lyssikatos C; Stratakis CA; Bostanjopoulou S
Int J Neurosci; 2022 Jul; 132(7):649-655. PubMed ID: 33027596
[TBL] [Abstract][Full Text] [Related]
17.
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]
18. Somatic PRKAR1A mutation in sporadic atrial myxoma with cerebral parenchymal metastases: a case report.
Roque A; Kimbrough T; Traner C; Baehring JM; Huttner A; Adams J; Canosa S; Sklar J; Madri JA
J Med Case Rep; 2019 Dec; 13(1):389. PubMed ID: 31874650
[TBL] [Abstract][Full Text] [Related]
19. A novel PRKAR1A gene mutation in Carney complex.
Chen W; Wang X
Clin Exp Dermatol; 2022 Feb; 47(2):476-479. PubMed ID: 34611929
[No Abstract] [Full Text] [Related]
20. Cutaneous signs are important in the diagnosis of the rare neoplasia syndrome Carney complex.
Vandersteen A; Turnbull J; Jan W; Simpson J; Lucas S; Anderson D; Lin JP; Stratakis C; Pichert G; Lim M
Eur J Pediatr; 2009 Nov; 168(11):1401-4. PubMed ID: 19219454
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]