Proteomic Approaches and Potential Applications in Autosomal Dominant Polycystic Kidney Disease and Fabry Disease

Although rare, hereditary diseases, such as autosomal dominant polycystic kidney disease (ADPKD) and Fabry disease (FD) may significantly progress towards severe nephropathy. It is crucial to characterize it accurately, predict the course of the illness and estimate treatment effectiveness. A huge e...

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Detalles Bibliográficos
Autores principales: Rroji, Merita, Figurek, Andreja, Spasovski, Goce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047122/
https://www.ncbi.nlm.nih.gov/pubmed/36980460
http://dx.doi.org/10.3390/diagnostics13061152

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047122/
https://www.ncbi.nlm.nih.gov/pubmed/36980460
http://dx.doi.org/10.3390/diagnostics13061152

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