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Sindrome da insufficienza cortico-surrenalica primitiva: nuovi concetti eziopatogenetici e diagnostici
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  • 作者:Stefano Laureti ; Prof. Fausto Santeusanio ; Alberto Falorni
  • 刊名:L'Endocrinologo
  • 出版年:2001
  • 出版时间:March 2001
  • 年:2001
  • 卷:2
  • 期:1
  • 页码:18-27
  • 全文大小:
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    8.Falorni A, Nikoshkov A, Laureti S, Greenback E, Hulting AL, Casucci G, Santeusanio F, Brunetti P, Luthman H, Lernmark 脜. High diagnostic accuracy for idiopathic Addison鈥檚 disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase. J Clin Endocrinol Metab 80: 2752, 1995.PubMed
    9.Colls J, Betterle C, Volpato M, Prentice L, Rees-Smith B, Furmaniak J. Immunoprecipitation assay for autoantibodies to steroid 21-hydroxylase in autoimmune adrenal diseases. Clin Chem 41: 375, 1995.PubMed
    10.Falorni A, Laureti S, Nikoshkov A, Picchio ML, Hallengren B, Vandewalle CL, Gorus FK, Belgian Diabetes Registry, Tortoioli C, Brunetti P, Santeusanio F. 21-hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison鈥檚 disease. Clin Exp Immunol 107: 341, 1997.PubMed Central PubMed CrossRef
    11.Laureti S, Falorni A, Volpato M, Casucci G, Picchio ML, Angeletti G, Luthman H, Brunetti P, Betterle C, Santeusanio F. Absence of circulating adrenal autoantibodies in adult-onset X-linked adrenoleukodystrophy. Horm Metab Res 28: 319, 1996.PubMed CrossRef
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    15.Achermann JC, Meeks JJ, Jameson JL. X-linked adrenal hypoplasia congenita and DAX1. The Endocrinologist 10: 289, 2000.CrossRef
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    17.Clark AJL, McLoughlin L, Grossman A. Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor. Lancet 341: 461, 1993.PubMed CrossRef
    18.Papadopoulos KI, Hallengren B. Polyglandular autoimmune syndrome type II in patients with idiopathic Addison鈥檚 disease. Acta Endocrinol (Copenh) 122: 472, 1990.
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    21.The Finnish-German APECED Consortium. An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains. Nat Genet 17: 399, 1997.CrossRef
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    23.Gambelunghe G, Falorni A, Ghaderi M, Laureti S, Tortoioli C, Santeusanio F, Brunetti P, Sanjeevi CB. Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison鈥檚 disease. J Clin Endocrinol Metab 84: 3701, 1999.PubMed
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    26.Laureti S, De Bellis AM, Muccitelli VI, Calcinaro F, Bizzarro A, Rossi R, Bellastella A, Santeusanio F, Falorni A. Levels of adrenocortical autoantibodies correlate with the degree of adrenal dysfunction in subjects with preclinical Addison鈥檚 disease. J Clin Endocrinol Metab 83: 3507, 1998.PubMed
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    30.Silva RC, Kater CE, Dib SA, Laureti S, Forini F, Cosentino A, Falorni A. Autoantibodies against recombinant human steroidogenic enzymes 21-hydroxylase, side-chain cleavage and 17伪-hydroxylase in Addison鈥檚 disease and autoimmune polyendocrine syndrome type III. Eur J Endocrinol 142: 187, 2000.CrossRef
    31.Perniola R, Falorni A, Clemente MG, Forini F, Accogli E, Lobreglio G. Organ-specific and non-organ-specific autoantibodies in children and young adults with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. Eur J Endocrinol 143: 497, 2000.PubMed CrossRef
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    36.Tsigos C, Arai K, Latronico AC, DiGeorge A, Rapaport R, Chrousos GP. A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome. J Clin Endocrinol Metab 80: 2186, 1995.PubMed
    37.Allgrove J, Clayden GS, Grant BD, Mccaulay JC. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet I: 1284, 1978.CrossRef
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  • 作者单位:Stefano Laureti (1)
    Prof. Fausto Santeusanio (1)
    Alberto Falorni (1)

    1. Dipartimento di Medicina Interna e Scienze Endocrine e Metaboliche, Universit脿 degli Studi di Perugia, Via Enrico Dal Pozzo, 06126, Perugia, Italia
  • 刊物类别:Medicine/Public Health, general; Endocrinology; Metabolic Diseases; Internal Medicine;
  • 刊物主题:Medicine/Public Health, general; Endocrinology; Metabolic Diseases; Internal Medicine;
  • 出版者:Springer International Publishing
  • ISSN:1720-8351
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