Results 11 to 20 of about 2,425,371 (368)

Correlation of the Dietary Protein Intake between Those Estimated from a Short Protein Food-Recall Questionnaire and from 24-Hour Urinary Urea-Nitrogen Excretion in Stages 3-4 Chronic Kidney Disease Patients

open access: yesInternational Journal of Nephrology, 2023
Introduction. High protein intake may accelerate progression of chronic kidney disease (CKD). Estimation of dietary protein intake (DPI) is indispensable for management of CKD, but to achieve optimum DPI is quite challenging in routine clinical practice.
Teerawat Thanachayanont   +4 more
doaj   +1 more source

Bedside Assessment of the Kidneys and Bladder Using Point of Care Ultrasound

open access: yesPOCUS Journal, 2022
Given the contrasting echogenic characteristics of the urinary system and their easily identifiable distortion in response to numerous pathologic processes, the sonographic examination of the kidney and bladder can provide a wealth of clinical ...
Patrick J. Taus   +2 more
doaj   +1 more source

Kidney [PDF]

open access: yesAmerican Journal of Transplantation, 2016
Kidney transplant provides significant survival, cost, and quality-of-life benefits over dialysis in patients with end-stage kidney disease, but the number of kidney transplant candidates on the waiting list continues to grow annually. By the end of 2014, nearly 100,000 adult candidates and 1500 pediatric candidates were waiting for kidney transplant ...
A, Hart   +10 more
openaire   +2 more sources

Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial. [PDF]

open access: yes, 2023
BACKGROUND: The EMPA-KIDNEY trial showed that empagliflozin reduced the risk of the primary composite outcome of kidney disease progression or cardiovascular death in patients with chronic kidney disease mainly through slowing progression.
EMPA-KIDNEY Collaborative Group
core   +1 more source

Emerging key roles for P2X receptors in the kidney [PDF]

open access: yes, 2013
P2X ionotropic non-selective cation channels are expressed throughout the kidney and are activated in a paracrine or autocrine manner following the binding of extracellular ATP and related extracellular nucleotides.
Peppiatt-Wildman, Claire M.   +10 more
core   +1 more source

Editor's note

open access: yesJournal of Kidney Cancer and VHL, 2014
Dear fellow researchers,Welcome to the first issue of the Journal of Kidney Cancer and VHL (JKCVHL).JKCVHL is an open access journal created to fill the vacuum for a specialized journal to disseminate information on the advances in kidney cancer and VHL ...
Journal of Kidney Cancer and VHL
doaj   +1 more source

Kidney age, not kidney disease [PDF]

open access: yesCanadian Medical Association Journal, 2018
KEY POINTS Although a variety of conditions and syndromes may affect the kidneys over either chronic or acute time frames, the term “chronic kidney disease” (CKD) is used to describe a decrease in the filtration ability of the glomerular capillaries in the kidney.
Stevens, Richard J   +10 more
openaire   +6 more sources

Seasonal mortality trends for hospitalised patients with acute kidney injury across England

open access: yesBMC Nephrology, 2023
Background Incidence of acute kidney injury (AKI) is known to peak in winter months. This is likely influenced by seasonality of commonly associated acute illnesses.
Esther Wong   +6 more
doaj   +1 more source

Paired and altruistic kidney donation in the UK: algorithms and experimentation [PDF]

open access: yes, 2012
We study the computational problem of identifying optimal sets of kidney exchanges in the UK. We show how to expand an integer programming-based formulation [1, 19] in order to model the criteria that constitute the UK definition of optimality.
David F. Manlove   +3 more
core   +1 more source

Kidney: polycystic kidney disease [PDF]

open access: yesWIREs Developmental Biology, 2014
Polycystic kidney disease (PKD) is a life‐threatening genetic disorder characterized by the presence of fluid‐filled cysts primarily in the kidneys. PKD can be inherited as autosomal recessive (ARPKD) or autosomal dominant (ADPKD) traits. Mutations in either the PKD1 or PKD2 genes, which encode polycystin 1 and polycystin 2, are the underlying cause of
Binu M, Paul, Gregory B, Vanden Heuvel
openaire   +2 more sources

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