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
Progressive vascular calcification in autoimmune polyglandular syndrome type I
β Scribed by S. Ohga; Naoko Matsumoto; Hidetoshi Takada; Akihiko Nomura; Tetsuo Matsuda; Toshiro Hara
- Publisher
- Springer-Verlag
- Year
- 2001
- Tongue
- English
- Weight
- 50 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0301-0449
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## Abstract Patients with autoimmune polyglandular syndrome type I (APS1) often display high titers of autoantibodies (autoAbs) directed against aromatic Lβamino 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 Lβamino acid decarboxylase (AADC), tyrosine hydroxylase (TH), tryptophan hydroxylase (TPH), and glutamic acid decarboxylase (GAD). Neurological s