157 related articles for article (PubMed ID: 38252880)
21. 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]
22. Clinical and molecular genetics of Carney complex.
Rothenbuhler A; Stratakis CA
Best Pract Res Clin Endocrinol Metab; 2010 Jun; 24(3):389-99. PubMed ID: 20833331
[TBL] [Abstract][Full Text] [Related]
23. Predicting the risk of cardiac myxoma in Carney complex.
Pitsava G; Zhu C; Sundaram R; Mills JL; Stratakis CA
Genet Med; 2021 Jan; 23(1):80-85. PubMed ID: 32893266
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Case Report: An Atypical Case of Carney Complex.
Khan Z; Alkhatib H; Ramani GV
Am J Case Rep; 2021 Oct; 22():e933744. PubMed ID: 34689149
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.
Salpea P; Horvath A; London E; Faucz FR; Vetro A; Levy I; Gourgari E; Dauber A; Holm IA; Morrison PJ; Keil MF; Lyssikatos C; Smith ED; Sanidad MA; Kelly JC; Dai Z; Mowrey P; Forlino A; Zuffardi O; Stratakis CA
J Clin Endocrinol Metab; 2014 Jan; 99(1):E183-8. PubMed ID: 24170103
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. A novel 8.57-kb deletion of the upstream region of PRKAR1A in a family with Carney complex.
Ito S; Hashimoto A; Yamaguchi K; Kawamura S; Myoen S; Ogawa M; Sato I; Minato T; Miyabe S; Nakazato A; Fujii K; Mochizuki M; Fujimori H; Tamai K; Niihori T; Aoki Y; Sugawara A; Sasano H; Shima H; Yasuda J
Mol Genet Genomic Med; 2022 Mar; 10(3):e1884. PubMed ID: 35128829
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. 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]
34. 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]
35. 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]
36. Fatal Carney Complex in Siblings Due to De Novo Large Gene Deletion.
Stelmachowska-Banas M; Zgliczynski W; Tutka P; Carney JA; Korbonits M
J Clin Endocrinol Metab; 2017 Nov; 102(11):3924-3927. PubMed ID: 28973408
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Association of the M1V PRKAR1A mutation with primary pigmented nodular adrenocortical disease in two large families.
Pereira AM; Hes FJ; Horvath A; Woortman S; Greene E; Bimpaki E; Alatsatianos A; Boikos S; Smit JW; Romijn JA; Nesterova M; Stratakis CA
J Clin Endocrinol Metab; 2010 Jan; 95(1):338-42. PubMed ID: 19915019
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
