Results 31 to 40 of about 1,561 (140)

Effect of urine pH changed by dietary intervention on uric acid clearance mechanism of pH-dependent excretion of urinary uric acid

open access: yesNutrition Journal, 2012
Background The finding reported in a previous paper - alkalization of urine facilitates uric acid excretion - is contradictory to what one might expect to occur: because food materials for the alkalization of urine contain fewer purine bodies than those ...
Kanbara Aya   +4 more
doaj   +1 more source

Case report: Severe rhabdomyolysis and acute liver injury in a high-altitude mountain climber

open access: yesFrontiers in Medicine, 2022
Concurrent severe rhabdomyolysis and acute liver damage are rarely reported in the setting of acute high-altitude illness (AHAI). We described a 53-year-old healthy mountain climber who experienced headache and dyspnea at the summit of Snow Mountain ...
Yun-Chih Yeh   +3 more
doaj   +1 more source

Rotavirus gastroenteritis-associated urinary tract calculus in an infant

open access: yesThe Turkish Journal of Pediatrics, 2018
Rotavirus gastroenteritis a severe viral gastroenteritis that occasionally causes post-renal failure with urinary tract calculus. A 15-month-old boy with rotavirus gastroenteritis suffered from pre- and post-renal dysfunction due to dehydration and ...
Kiwako Tsukida   +5 more
doaj   +1 more source

Ochronotic Arthropathy: A Report of Two Cases

open access: yesSouthern Clinics of Istanbul Eurasia, 2020
Ochronosis is an entity characterized by deposition of homogentisic acid and metabolites in connective tissues, such as joint cartilage, skin and sclera.
Selma Şengiz Erhan   +3 more
doaj   +1 more source

Alkaline-encrusting pyelitis – A rare disastrous complication postPCNL leading to chronic renal failure

open access: yesIndian Journal of Urology, 2019
Alkaline-encrusting pyelitis (AEP) is a severe form of infectious disease characterized by encrustation along the lining of the urinary tract leading to loss of renal function.
Kalpesh Parmar   +2 more
doaj   +1 more source

The Role of Urine Alkalinization in Preventing Rhabdomyolysis-Induced Acute Kidney Injury and Need for Dialysis: A Systematic Review and Meta-Analysis [PDF]

open access: yesBulletin of Emergency and Trauma
Objective: This systematic review and meta-analysis aimed to evaluate the efficacy of urine alkalinization in preventing acute kidney injury (AKI) and the need for dialysis in patients with rhabdomyolysis.Methods: This study was conducted in accordance ...
Saeed Safari   +6 more
doaj   +1 more source

Prolapsed lumbar disc in alkaptonuria

open access: yesJournal of Dr. NTR University of Health Sciences, 2016
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by deficiency of homogentisate 1,2-dioxygenase, an enzyme that converts homogentisic acid (HGA) to maleylacetoacetic acid in the tyrosine degradation pathway.
Surapaneni Suresh Babu   +3 more
doaj   +1 more source

GC-MS Analysis of Biological Nitrate and Nitrite Using Pentafluorobenzyl Bromide in Aqueous Acetone: A Dual Role of Carbonate/Bicarbonate as an Enhancer and Inhibitor of Derivatization

open access: yesMolecules, 2021
Carbon dioxide (CO2) and carbonates, which are widely distributed in nature, are constituents of inorganic and organic matter and are essential in vegetable and animal organisms. CO2 is the principal greenhouse gas in the atmosphere.
Dimitrios Tsikas
doaj   +1 more source

Unraveling the Potential of MXenes in Electrochemical Sensing: Mechanistic Insight, Design Principles, and Analytical Applications

open access: yesSmall Science, Volume 6, Issue 5, May 2026.
This review comprehensively examines recent progress in MXene‐based electrochemical sensors for the detection of glucose, hydrogen peroxide, heavy metals, pesticides, nitrites, phenolic pollutants, neurotransmitters, biomarkers, and pharmaceutical compounds.
Hichem Moulahoum   +3 more
wiley   +1 more source

Isolated Kidney Transplant in Primary Hyperoxaluria‐1 Enabled by Small Interfering RNA (siRNA) Therapy. Is It Time for Change? Case Report and Review of the Literature

open access: yesPediatric Transplantation, Volume 30, Issue 5, May 2026.
ABSTRACT Background Primary hyperoxaluria type 1 (PH1) is a rare genetic disorder characterized by excessive oxalate production that leads to nephrocalcinosis or nephrolithiasis and progressive kidney failure, associated with systemic oxalosis that is not reversed by dialysis. Pharmacological treatment is limited.
Shameer M. Habeeb   +8 more
wiley   +1 more source

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