Results 11 to 20 of about 5,638,461 (310)

Ferroptosis and kidney disease

open access: yesNefrología (English Edition), 2020
La muerte celular es un proceso minuciosamente regulado que se desarrolla a través de diferentes vías. La muerte celular regulada, ya sea mediante apoptosis o necrosis regulada, ofrece la posibilidad de introducir una intervención terapéutica.
Fontecha-Barriuso, Miguel   +8 more
core   +4 more sources

Kidney diseases

open access: yesImmunological Reviews, 2022
SummaryDysregulation and accelerated activation of the alternative pathway (AP) of complement is known to cause or accentuate several pathologic conditions in which kidney injury leads to the appearance of hematuria and proteinuria and ultimately to the development of chronic renal failure.
Erica Daina   +2 more
openaire   +2 more sources

Serum PTH Associated with Malnutrition Determined by Bioelectrical Impedance Technology in Chronic Kidney Disease Patients

open access: yesInternational Journal of Endocrinology, 2022
Purpose. Chronic malnutrition and cachexia are common in chronic kidney disease (CKD), and importance should be given to these complications because they affect the patient’s quality of life and prognosis.
Lilin Liu   +6 more
doaj   +1 more source

Prescription characteristics of phosphate binders in a high pill burden for hemodialysis patients

open access: yesRenal Replacement Therapy, 2021
Background Dialysis patients have to take many oral drugs, causing a high pill burden. Phosphate binders (PBs) account for a large proportion of daily pill burden; however, the relationship between patient background and prescription status of PBs is not
Nobuo Nagano   +8 more
doaj   +1 more source

Successful treatment of nephrotic syndrome due to pregnancy-related crescentic IgA nephropathy: a case report

open access: yesBMC Nephrology, 2023
Background Crescentic immunoglobulin A (IgA) nephropathy, defined as > 50% of the glomeruli with crescents, often has a poor renal prognosis. Because of the high prevalence of pre-eclampsia in the second trimester of pregnancy, we often fail to ...
Hisato Shima   +8 more
doaj   +1 more source

A retrospective study of patients with Stenotrophomonas maltophilia peritonitis undergoing peritoneal dialysis

open access: yesRenal Replacement Therapy, 2023
Background Stenotrophomonas maltophilia (S. maltophilia) is being increasingly recognized as an important cause of nosocomial infections, particularly in immunocompromised patients, such as patients undergoing dialysis. S.
Hisato Shima   +8 more
doaj   +1 more source

Extended infusion of rituximab combined with steroids is effective in inducing remission and reducing relapse in adult minimal change disease

open access: yesBMC Nephrology, 2021
Background Minimal change disease is a common cause of nephrotic syndrome in adults. Higher relapse rate put patients at risk of steroids toxicity due to long-term exposure.
Diankun Liu   +8 more
doaj   +1 more source

The Comparison of the Kidney Effects of Dipeptidyl Peptidase 4 Inhibitors and Glucagon-Like Peptide 1 Agonist-Administered Concomitant with Sodium-Glucose Cotransporter 2 Inhibitors in Japanese Patients with Type 2 Diabetes Mellitus and Chronic Kidney Disease

open access: yesJournal of Diabetes Research, 2021
Background and Aim. Strong evidence exists supporting the utility of sodium glucose cotransporter inhibitors (SGLT2is) for treating not only cardiovascular events but also renal events.
Kazuo Kobayashi   +6 more
doaj   +1 more source

Effect of a Hemodialysis Session on Markers of Inflammation and Endotoxin

open access: yesInternational Journal of Inflammation, 2022
Background. People receiving hemodialysis (HD) treatment have higher cardiovascular morbidity and mortality, ascribed to an increased prevalence of traditional cardiovascular risk factors.
Shyam Dheda   +4 more
doaj   +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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