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...

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Detalles Bibliográficos
Autores principales: Hanssens, Laurence S., Cellauro, Sarah, Duchateau, Jean, Casimir, Georges J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
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

Internet

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

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