Results 91 to 100 of about 6,399 (205)

Modulation of renal inflammation and tubular injury by calcitriol in patients with early diabetic kidney disease: a randomized controlled trial

open access: yesAnnals of Medicine
Introduction Diabetic kidney disease (DKD) is marked by inflammation, fibrosis and oxidative stress. Calcitriol may offer renoprotective effects by modulating these processes.
Pringgodigdo Nugroho   +6 more
doaj   +1 more source

Clinicopathological findings, correlations and outcomes in patients with renal disease and living with antiretroviral‐treated human immunodeficiency virus infection

open access: yesInternal Medicine Journal, Volume 56, Issue 8, Page 1402-1411, August 2026.
Abstract Background and Aims Antiretroviral therapy (ART) has modified the incidence of renal complications and the patterns of renal disease in people living with Human Immunodeficiency Virus (PLWH). We reviewed (2011–2021) the progress and outcomes (follow‐up to mid‐2025) of 158 such individuals.
Jacqueline A. Evans   +5 more
wiley   +1 more source

Approach to a Child with Hypophosphatemia

open access: yesBiomolecules
Hypophosphatemia is a rare ion disorder in children, but it carries the risk of serious clinical sequelae in tissues and organs with high energy requirements, such as bone tissue.
Agnieszka Antonowicz   +3 more
doaj   +1 more source

Australian Standards of Care for Genetic and Genomic Testing in Kidney Disease, Chapter 4

open access: yes
Internal Medicine Journal, Volume 56, Issue S5, Page 15-17, November 2026.
Sadia Jahan   +10 more
wiley   +1 more source

Australian Standards of Care for Genetic and Genomic Testing in Kidney Disease, Chapter 5

open access: yes
Internal Medicine Journal, Volume 56, Issue S5, Page 18-20, November 2026.
Sadia Jahan   +10 more
wiley   +1 more source

Home Parenteral Support in Severe Gitelman Syndrome: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Gitelman syndrome (GS), also known as familial hypokalaemia‐hypomagnesemia, is a rare autosomal recessive renal tubular disorder characterized by hypokalaemia, hypomagnesemia, metabolic alkalosis, and hypocalciuria. Electrolyte replacement of potassium and magnesium remains the mainstay of management, with oral supplementation achieving this ...
Georgia Martin   +2 more
wiley   +1 more source

Australian Guideline for the Identification and Management of Hypertension in Children and Adolescents

open access: yes
Journal of Paediatrics and Child Health, Volume 62, Issue 10, Page 1822-1847, October 2026.
N. G. Larkins   +28 more
wiley   +1 more source

Long Term Follow‐Up After Transplantation in Propionic Acidemia: A Retrospective French Pediatric and Adult Cohort Study

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 4, July 2026.
ABSTRACT Propionic acidemia (PA) is a rare inherited metabolic disorder associated with recurrent metabolic decompensations and chronic multisystemic complications. Liver transplantation (LT) may improve metabolic stability, but its long‐term impact on organ involvement remains debated.
Tristan Mekdade   +25 more
wiley   +1 more source

Glycated Albumin Is a More Useful Glycation Index than HbA1c for Reflecting Renal Tubulopathy in Subjects with Early Diabetic Kidney Disease [PDF]

open access: yes, 2018
BackgroundThe aim of this study was to investigate which glycemic parameters better reflect urinary N-acetyl-β-D-glucosaminidase (uNAG) abnormality, a marker for renal tubulopathy, in subjects with type 2 diabetes mellitus (T2DM) subjects with ...
Jae Hyeon Kim   +4 more
core   +2 more sources

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness

open access: yes, 2021
Background: The transepithelial transport of electrolytes, solutes, and water in the kidney is a well-orchestrated process involving numerous membrane transport systems. Basolateral potassium channels in tubular cells not only mediate potassium recycling
Atanasov, Velko   +9 more
core   +1 more source

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