189 related articles for article (PubMed ID: 35732416)
1. 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]
2. [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]
3. 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]
4. 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]
5. Carney complex due to a novel pathogenic variant in the PRKAR1A gene - a case report.
Ferreira SH; Costa MM; Rios E; Santos Silva R; Costa C; Castro-Correia C; Fontoura M
J Pediatr Endocrinol Metab; 2019 Feb; 32(2):197-202. PubMed ID: 30699069
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. A novel PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease and the Carney complex.
Peck MC; Visser BC; Norton JA; Pasche L; Katznelson L
Endocr Pract; 2010; 16(2):198-204. PubMed ID: 19833579
[TBL] [Abstract][Full Text] [Related]
10. Carney Complex Complicated with Primary Pigmented Nodular Adrenocortical Disease without Cushing's Syndrome Recurrence for Five Years after Unilateral Adrenalectomy.
Tsurutani Y; Kiriyama K; Kondo M; Hasebe M; Sata A; Mizuno Y; Sugisawa C; Saito J; Nishikawa T
Intern Med; 2022; 61(2):205-211. PubMed ID: 35034934
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Hormonal, Radiological, NP-59 Scintigraphy, and Pathological Correlations in Patients With Cushing's Syndrome Due to Primary Pigmented Nodular Adrenocortical Disease (PPNAD).
Vezzosi D; Tenenbaum F; Cazabat L; Tissier F; Bienvenu M; Carrasco CA; Laloi-Michelin M; Barrande G; Lefebvre H; Hiéronimus S; Tabarin A; Bertagna X; Legmann P; Vantyghem MC; Bertherat J
J Clin Endocrinol Metab; 2015 Nov; 100(11):4332-8. PubMed ID: 26390100
[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. 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. PubMed ID: 12213893
[TBL] [Abstract][Full Text] [Related]
16. An unusual presentation of Carney complex with diffuse primary pigmented nodular adrenocortical disease on one adrenal gland and a nonpigmented adrenocortical adenoma and focal primary pigmented nodular adrenocortical disease on the other.
Tung SC; Hwang DY; Yang JW; Chen WJ; Lee CT
Endocr J; 2012; 59(9):823-30. PubMed ID: 22785148
[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. 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. PubMed ID: 16464939
[TBL] [Abstract][Full Text] [Related]
19. Bilateral primary pigmented nodular adrenal disease as a component of Carney syndrome - case report.
Sikorska D; Bednarek-Papierska L; Mojs E; Makowska E; Ruchała M; Samborski W
Endokrynol Pol; 2017; 68(1):70-72. PubMed ID: 28255981
[TBL] [Abstract][Full Text] [Related]
20. Carney complex (CNC).
Bertherat J
Orphanet J Rare Dis; 2006 Jun; 1():21. PubMed ID: 16756677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]