A questionnaire survey on the diagnosis and treatment of Fabry nephropathy in clinical practice

BACKGROUND: Fabry nephropathy is characterized by a deficiency of lysosomal alpha-galactosidase A, which results in proteinuria and kidney disease. The ineffectiveness of enzyme replacement therapy (ERT) for severe kidney failure highlights the need for early detection and meaningful markers. Howeve...

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Detalles Bibliográficos
Autores principales: Choi, Soo Jeong, Kim, Su Hyun, Lee, Min Sung, Park, Samel, Cho, Eunjung, Han, Seung Seok, Koh, Eun Sil, Chung, Byung Ha, Jeong, Kyung Hwan, Bae, Eun Hui, Lee, Eun Young, Kwon, Young Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Nephrology 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565450/
https://www.ncbi.nlm.nih.gov/pubmed/37448283
http://dx.doi.org/10.23876/j.krcp.22.235

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565450/
https://www.ncbi.nlm.nih.gov/pubmed/37448283
http://dx.doi.org/10.23876/j.krcp.22.235

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