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Journal Abstract Search

321 related items for PubMed ID: 21047926

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  • 4. 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
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  • 5. Phosphodiesterase 11A expression in the adrenal cortex, primary pigmented nodular adrenocortical disease, and other corticotropin-independent lesions.
    Boikos SA, Horvath A, Heyerdahl S, Stein E, Robinson-White A, Bossis I, Bertherat J, Carney JA, Stratakis CA.
    Horm Metab Res; 2008 May; 40(5):347-53. PubMed ID: 18491255
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  • 7. An Unusual Presentation of Carney Complex.
    Dağdeviren Çakır A, Turan H, Celkan T, Çomunoğlu N, Ercan O, Evliyaoğlu O.
    J Clin Res Pediatr Endocrinol; 2020 Mar 19; 12(1):117-121. PubMed ID: 31117334
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  • 8. 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 19; 97(3):E496-502. PubMed ID: 22205709
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  • 16. PRKAR1A mutation causing pituitary-dependent Cushing disease in a patient with Carney complex.
    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 19; 177(2):K7-K12. PubMed ID: 28522647
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  • 17. An adolescent with large cell calcifying sertoli cell tumor of the testis and undiagnosed Carney Complex: A case report.
    Rosenblum F, Koenig RG, Mikhail FM, Porterfield JR, Nix JW, Eltoum IA.
    Diagn Cytopathol; 2017 Jul 19; 45(7):634-639. PubMed ID: 28276158
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