A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1

CONTEXT: Autoimmune polyendocrine syndrome type 1 (APS1) is a childhood-onset monogenic disease defined by the presence of two of the three major components: hypoparathyroidism, primary adrenocortical insufficiency, and chronic mucocutaneous candidiasis (CMC). Information on longitudinal follow-up o...

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Detalles Bibliográficos
Autores principales: Bruserud, Øyvind, Oftedal, Bergithe E., Landegren, Nils, Erichsen, Martina M., Bratland, Eirik, Lima, Kari, Jørgensen, Anders P., Myhre, Anne G., Svartberg, Johan, Fougner, Kristian J., Bakke, Åsne, Nedrebø, Bjørn G., Mella, Bjarne, Breivik, Lars, Viken, Marte K., Knappskog, Per M., Marthinussen, Mihaela C., Løvås, Kristian, Kämpe, Olle, Wolff, Anette B., Husebye, Eystein S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971337/
https://www.ncbi.nlm.nih.gov/pubmed/27253668
http://dx.doi.org/10.1210/jc.2016-1821

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971337/
https://www.ncbi.nlm.nih.gov/pubmed/27253668
http://dx.doi.org/10.1210/jc.2016-1821

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