Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages

Progressive familial intrahepatic cholestasis type 1 (PFIC1), a rare inherited recessive disease resulting from a genetic deficiency in ATP8B1, progresses to liver failure. Because of the difficulty of discriminating PFIC1 from other subtypes of PFIC based on its clinical and histological features a...

Descripción completa

Detalles Bibliográficos
Autores principales: Hayashi, Hisamitsu, Naoi, Sotaro, Togawa, Takao, Hirose, Yu, Kondou, Hiroki, Hasegawa, Yasuhiro, Abukawa, Daiki, Sasaki, Mika, Muroya, Koji, Watanabe, Satoshi, Nakano, Satoshi, Minowa, Kei, Inui, Ayano, Fukuda, Akinari, Kasahara, Mureo, Nagasaka, Hironori, Bessho, Kazuhiko, Suzuki, Mitsuyoshi, Kusuhara, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828058/
https://www.ncbi.nlm.nih.gov/pubmed/29104077
http://dx.doi.org/10.1016/j.ebiom.2017.10.007

Ejemplares similares

Ejemplares similares