These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

240 related items for PubMed ID: 12373631

  • 1. Familial ACTH-independent Cushing's syndrome with bilateral macronodular adrenal hyperplasia clinically affecting only female family members.
    Nies C, Bartsch DK, Ehlenz K, Wild A, Langer P, Fleischhacker S, Rothmund M.
    Exp Clin Endocrinol Diabetes; 2002 Sep; 110(6):277-83. PubMed ID: 12373631
    [Abstract] [Full Text] [Related]

  • 2. Familial vasopressin-sensitive ACTH-independent macronodular adrenal hyperplasia (VPs-AIMAH): clinical studies of three kindreds.
    Gagliardi L, Hotu C, Casey G, Braund WJ, Ling KH, Dodd T, Manavis J, Devitt PG, Cutfield R, Rudzki Z, Scott HS, Torpy DJ.
    Clin Endocrinol (Oxf); 2009 Jun; 70(6):883-91. PubMed ID: 19018784
    [Abstract] [Full Text] [Related]

  • 3. Familial Cushing's syndrome. Micronodular adrenocortical dysplasia.
    Hodge BO, Froesch TA.
    Arch Intern Med; 1988 May; 148(5):1133-6. PubMed ID: 3365080
    [Abstract] [Full Text] [Related]

  • 4. Adrenocorticotropic hormone-independent Cushing's syndrome.
    Bourdeau I, Lampron A, Costa MH, Tadjine M, Lacroix A.
    Curr Opin Endocrinol Diabetes Obes; 2007 Jun; 14(3):219-25. PubMed ID: 17940443
    [Abstract] [Full Text] [Related]

  • 5. [Cushing's syndrome due to bilateral adrenal macronodular hyperplasia. From ACTH-dependent hypercortisolism to ACTH-independent hypercortisolism].
    López JM, Sapunar J, Donoso J, Martínez P.
    Rev Med Chil; 1991 Oct; 119(10):1165-70. PubMed ID: 1668993
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. ARMC5 mutations in a large French-Canadian family with cortisol-secreting β-adrenergic/vasopressin responsive bilateral macronodular adrenal hyperplasia.
    Bourdeau I, Oble S, Magne F, Lévesque I, Cáceres-Gorriti KY, Nolet S, Awadalla P, Tremblay J, Hamet P, Fragoso MC, Lacroix A.
    Eur J Endocrinol; 2016 Jan; 174(1):85-96. PubMed ID: 26604299
    [Abstract] [Full Text] [Related]

  • 16. ACTH independent Cushing's syndrome occurring in siblings.
    Minami S, Sugihara H, Sato J, Tatsukuchi A, Sugisaki Y, Sasano H, Wakabayashi I.
    Clin Endocrinol (Oxf); 1996 Apr; 44(4):483-8. PubMed ID: 8706318
    [Abstract] [Full Text] [Related]

  • 17. Familial adrenocorticotropin-independent macronodular adrenal hyperplasia with aberrant serotonin and vasopressin adrenal receptors.
    Vezzosi D, Cartier D, Régnier C, Otal P, Bennet A, Parmentier F, Plantavid M, Lacroix A, Lefebvre H, Caron P.
    Eur J Endocrinol; 2007 Jan; 156(1):21-31. PubMed ID: 17218722
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.