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Abelardo Aguilera

Researcher at Hospital Universitario La Paz

Publications -  86
Citations -  4439

Abelardo Aguilera is an academic researcher from Hospital Universitario La Paz. The author has contributed to research in topics: Peritoneal dialysis & Angiogenesis. The author has an hindex of 34, co-authored 86 publications receiving 4113 citations.

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Peritoneal Dialysis and Epithelial-to-Mesenchymal Transition of Mesothelial Cells

TL;DR: The results suggest that mesothelial cells have an active role in the structural and functional alteration of the peritoneum during peritoneal dialysis, and suggest potential targets for the design of new dialysis solutions and markers for the monitoring of patients.
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Epithelial to Mesenchymal Transition and Peritoneal Membrane Failure in Peritoneal Dialysis Patients: Pathologic Significance and Potential Therapeutic Interventions

TL;DR: Recent advances on understanding the mechanisms that are implicated in peritoneal structural alterations have allowed the identification of the EMT of MC as a potential therapeutic target of membrane failure, and this article provides a comprehensive review of recent advances.
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Mesenchymal Conversion of Mesothelial Cells as a Mechanism Responsible for High Solute Transport Rate in Peritoneal Dialysis: Role of Vascular Endothelial Growth Factor

TL;DR: It is suggested that mesothelial cells that have undergone epithelial-to-mesenchymal transition are the main source of VEGF in PD patients and therefore may be responsible for a high peritoneal transport rate.
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Risk factors for abdominal wall complications in peritoneal dialysis patients.

TL;DR: Abdominal hernias and peritoneal leaks are very frequent in the PD population and advanced age, polycystic kidney disease, and high body mass index are independent risk factors for their development.
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Blocking TGF-β1 Protects the Peritoneal Membrane from Dialysate-Induced Damage

TL;DR: It is demonstrated that TGF-β1 drives the peritoneal deterioration induced by dialysis fluid and highlights a role of TGF -β1-mediated MMT in the pathophysiology of peritoneale-membrane dysfunction.