Polyglandular Autoimmune Syndrome Type I
✍ Scribed by Emmanuelle Proust-Lemoine; Pascale Saugier-Veber; Jean-Louis Wémeau
- Book ID
- 118052885
- Publisher
- Masson Editeur
- Year
- 2012
- Tongue
- French
- Weight
- 257 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0755-4982
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📜 SIMILAR VOLUMES
Autoimmune polyglandular syndrome is characterized by a failure of multiple endocrine organs and the presence of circulating organ-specific autoantibodies targeted against the failing organs. Here we describe a patient with autoimmune polyglandular syndrome type I with the endocrine manifestations o
## Abstract Patients with autoimmune polyglandular syndrome type I (APS1) often display high titers of autoantibodies (autoAbs) directed against aromatic L‐amino acid decarboxylase (AADC), tyrosine hydroxylase (TH), tryptophan hydroxylase (TPH), and glutamic acid decarboxylase (GAD). Neurological s
## Abstract Patients with autoimmune polyglandular syndrome type I (APS1) often display high titers of autoantibodies (autoAbs) directed against aromatic L‐amino acid decarboxylase (AADC), tyrosine hydroxylase (TH), tryptophan hydroxylase (TPH), and glutamic acid decarboxylase (GAD). Neurological s