Long-term survival in Japanese renal transplant recipients with Alport syndrome: a retrospective study

BACKGROUND: Patients with Alport syndrome (AS) develop progressive kidney dysfunction due to a hereditary type IV collagen deficiency. Survival of the kidney allograft in patients with AS is reportedly excellent because AS does not recur. However, several studies have implied that the type IV collag...

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Detalles Bibliográficos
Autores principales: Katsuma, Ai, Nakada, Yasuyuki, Yamamoto, Izumi, Horita, Shigeru, Furusawa, Miyuki, Unagami, Kohei, Katsumata, Haruki, Okumi, Masayoshi, Ishida, Hideki, Yokoo, Takashi, Tanabe, Kazunari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171154/
https://www.ncbi.nlm.nih.gov/pubmed/30285655
http://dx.doi.org/10.1186/s12882-018-1052-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171154/
https://www.ncbi.nlm.nih.gov/pubmed/30285655
http://dx.doi.org/10.1186/s12882-018-1052-9

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