Results 81 to 90 of about 16,655 (259)

Robot‐assisted vs open kidney transplantation from deceased donors

open access: yesBJU International, Volume 136, Issue 3, Page 484-492, September 2025.
Objectives To test the hypothesis that the type of surgical approach, robot‐assisted kidney transplantation (RAKT) vs open kidney transplantation (OKT), impacts intra‐operative and postoperative surgical outcomes of patients receiving kidney transplantation from deceased donors.
Luca Afferi   +22 more
wiley   +1 more source

Il Registro Italiano del Rene PolicisticoAutosomico Dominante [PDF]

open access: yes, 2010
Non ...
A. Boletta   +12 more
core   +1 more source

Lactate and Lactylation in AKI‐to‐CKD: Epigenetic Regulation and Therapeutic Opportunities

open access: yesCell Proliferation, Volume 58, Issue 9, September 2025.
ABSTRACT Lactate is not only a byproduct of glycolysis, but is also considered an energy source, gluconeogenic precursor, signalling molecule and protein modifier during the process of cellular metabolism. The discovery of lactylation reveals the multifaceted functions of lactate in cellular metabolism and opens new avenues for lactate‐related research.
Yi Hou   +7 more
wiley   +1 more source

Progression of autosomal dominant kidney disease: measurement of the stage transitions of chronic kidney disease

open access: yesDrugs in Context, 2015
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a progressive genetic disorder characterized by the development of numerous kidney cysts that result in kidney failure.
Christopher M Blanchette   +7 more
doaj   +1 more source

Urinary proteomic biomarkers for diagnosis and risk stratification of autosomal dominant polycystic kidney disease: a multicentric study. [PDF]

open access: yesPLoS ONE, 2013
Treatment options for autosomal dominant polycystic kidney disease (ADPKD) will likely become available in the near future, hence reliable diagnostic and prognostic biomarkers for the disease are strongly needed.
Andreas D Kistler   +13 more
doaj   +1 more source

Dialysis Vintage and Symptom Burden in Hemodialysis: A Comprehensive Analysis

open access: yesNursing &Health Sciences, Volume 27, Issue 3, September 2025.
ABSTRACT End‐stage renal disease (ESRD) requires lifelong maintenance hemodialysis (MHD), and patients commonly experience a high symptom burden that affects their quality of life. This study explores the impact of dialysis vintage on symptom burden and quality of life in ESRD patients undergoing MHD.
Shanshan Yan   +4 more
wiley   +1 more source

The value of genotypic and imaging information to predict functional and structural outcomes in ADPKD [PDF]

open access: gold, 2020
Sravanthi Lavu   +16 more
openalex   +1 more source

Health-related quality of life across all stages of autosomal dominant polycystic kidney disease [PDF]

open access: yes, 2016
Background. A limited number of studies have assessed health related quality of life (HRQoL) in autosomal dominant polycystic kidney disease (ADPKD). Results to date have been conflicting and studies have generally focused on patients with later stages ...
Dieperink, Hans   +7 more
core   +2 more sources

Post‐Translational Modifications in Cilia and Ciliopathies

open access: yesAdvanced Science, Volume 12, Issue 31, August 21, 2025.
This review synthesizes current understanding of post‐translational modifications (PTMs) in ciliary proteins and emphasizes their roles in ciliary formation, homeostasis, and signaling. This review also discusses the implication of PTM dysregulation in ciliopathies and explores therapeutic strategies targeting PTM‐modifying enzymes.
Jie Ran, Jun Zhou
wiley   +1 more source

Autosomal dominant polycystic kidney disease: an overview of recent genetic and clinical advances

open access: yesRenal Failure
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common inherited kidney disease, characterized by the progressive development of multiple kidney cysts, leading to a gradual decline in kidney function.
Abdul Hamid Borghol   +5 more
doaj   +1 more source

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