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Immunoglobulin G: A useful outcome marker in the follow‐up of cystic fibrosis patients?
BACKGROUND AND METHODS: Hypergammaglobulinemia (hyper‐IgG) and hypogammaglobulinemia (hypo‐IgG) have been reported in patients with cystic fibrosis (CF). Although the clinical respiratory course is paradoxically different, depending on the IgG status, this association remains elusive. Therefore, we...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127551/ https://www.ncbi.nlm.nih.gov/pubmed/33783131 http://dx.doi.org/10.1002/iid3.426 |