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Journal Abstract Search

143 related items for PubMed ID: 24805858

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  • 5. 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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  • 9. The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review.
    Sun J, Ding L, He L, Fu H, Li R, Feng J, Dong J, Liao L.
    Front Endocrinol (Lausanne); 2024; 15():1356870. PubMed ID: 39006359
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  • 12. 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
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  • 13. Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia.
    Storr HL, Mitchell H, Swords FM, Main KM, Hindmarsh PC, Betts PR, Shaw NJ, Johnston DI, Clark AJ, Reznek RH, Grossman AB, Savage MO.
    Clin Endocrinol (Oxf); 2004 Nov; 61(5):553-9. PubMed ID: 15521956
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  • 14. Cushing syndrome in a young woman due to primary pigmented nodular adrenal disease.
    Hackman KL, Davis AL, Curnow PA, Serpell JW, McLean CA, Topliss DJ.
    Endocr Pract; 2010 Nov; 16(1):84-8. PubMed ID: 19703806
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  • 15. 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 Nov; 16(2):198-204. PubMed ID: 19833579
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  • 16. Primary adrenocortical nodular dysplasia as a cause of Cushing's syndrome in infants and children.
    McArthur RG, Bahn RC, Hayles AB.
    Mayo Clin Proc; 1982 Jan; 57(1):58-63. PubMed ID: 7054621
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  • 17. Familial micronodular adrenocortical disease, Cushing syndrome, and mutations of the gene encoding phosphodiesterase 11A4 (PDE11A).
    Carney JA, Gaillard RC, Bertherat J, Stratakis CA.
    Am J Surg Pathol; 2010 Apr; 34(4):547-55. PubMed ID: 20351491
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  • 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
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  • 20. 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 May; 68(1):70-72. PubMed ID: 28255981
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