Multiplex Autoantibody Detection in Patients with Autoimmune Polyglandular Syndromes

The diagnosis of autoimmune polyglandular syndrome (APS) types 1/2 is difficult due to their rarity and nonspecific clinical manifestations. APS-1 development can be identified with assays for autoantibodies against cytokines, and APS-2 development with organ-specific antibodies. In this study, a mi...

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Detalles Bibliográficos
Autores principales: Savvateeva, Elena N., Yukina, Marina Yu., Nuralieva, Nurana F., Filippova, Marina A., Gryadunov, Dmitry A., Troshina, Ekaterina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197071/
https://www.ncbi.nlm.nih.gov/pubmed/34071130
http://dx.doi.org/10.3390/ijms22115502

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197071/
https://www.ncbi.nlm.nih.gov/pubmed/34071130
http://dx.doi.org/10.3390/ijms22115502

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