Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

Aim: Cystic fibrosis (CF) is an autosomal recessive disorder. Although it is considered as an epithelial disease due to impaired chloride transport, its pathogenesis remains unclear. CF is classified as a syndrome with congenital defects of phagocyte in recent human inborn errors of immunity phenoty...

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Autores principales: Handan Duman Şenol (Autor), Meral Barlık (Autor), Ezgi Topyıldız (Autor), Figen Gülen (Autor), Güzide Aksu (Autor), Necil Kütükçüler (Autor), Esen Demir (Autor), Neslihan Edeer Karaca (Autor)
Formato: Libro
Publicado: Galenos Yayinevi, 2024-06-01T00:00:00Z.
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3rd Floor Main Library

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