Consensus statement on the diagnosis, treatment and follow‐up of patients with primary adrenal insufficiency

@article{Husebye2014ConsensusSO,
  title={Consensus statement on the diagnosis, treatment and follow‐up of patients with primary adrenal insufficiency},
  author={E. S. Husebye and B. Allolio and W. Arlt and K. Badenhoop and S. Bensing and C. Betterle and A. Falorni and E. H. Gan and A-L Hulting and A. Kasperlik-Załuska and O. K{\"a}mpe and K. Lovas and G. Meyer and S. Pearce},
  journal={Journal of Internal Medicine},
  year={2014},
  volume={275},
  pages={104 - 115}
}
  • E. S. Husebye, B. Allolio, +11 authors S. Pearce
  • Published 2014
  • Medicine
  • Journal of Internal Medicine
    • Primary adrenal insufficiency (PAI), or Addison's disease, is a rare, potentially deadly, but treatable disease. Most cases of PAI are caused by autoimmune destruction of the adrenal cortex. Consequently, patients with PAI are at higher risk of developing other autoimmune diseases. The diagnosis of PAI is often delayed by many months, and most patients present with symptoms of acute adrenal insufficiency. Because PAI is rare, even medical specialists in this therapeutic area rarely manage more… CONTINUE READING
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    References

    SHOWING 1-10 OF 35 REFERENCES
    Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I
    • 258
    Italian addison network study: update of diagnostic criteria for the etiological classification of primary adrenal insufficiency.
    • 86
    • PDF
    What is the best diagnostic and therapeutic management strategy for an Addison patient during pregnancy?
    • 56
    Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry.
    • 249
    • PDF
    Screening for associated autoimmune disorders in Polish patients with Addison’s disease
    • 43
    Autoimmune adrenal insufficiency and autoimmune polyendocrine syndromes: autoantibodies, autoantigens, and their applicability in diagnosis and disease prediction.
    • 603
    • PDF
    High Frequency of Coeliac Disease among Patients with Autoimmune Adrenocortical Failure
    • 60
    Risk of primary adrenal insufficiency in patients with celiac disease.
    • 53
    • PDF
    Adrenal autoantibodies and organ‐specific autoimmunity in patients with Addison's disease
    • 65
    Autoimmune Addison disease: pathophysiology and genetic complexity
    • 78