News

DISABLED ENTREPRENEUR UK on MSN10mon
Renal Tubular Acidosis PIP Eligibility
Renal Tubular Acidosis (RTA) is a complex kidney disorder that disrupts the body's acid-base balance, leading to a range of ...
Renal tubular acidosis may signal subclinical kidney involvement in patients with mutations in the TTR gene, according to new research.
Distal renal tubular acidosis is a serious orphan disease characterized by a lack of renal excretion of metabolically generated acids. The excess acid thus accumulated in the blood can lead to ...
Renal Tubular Transport Mechanisms and Acidosis Publication Trend The graph below shows the total number of publications each year in Renal Tubular Transport Mechanisms and Acidosis.
Distal renal tubular acidosis is a rare disease (it affects only about 1:100.000 people) and is congenital in most cases (also called familial or primary dRTA).
About dRTA Distal renal tubular acidosis dRTA is an orphan disease characterized by a failure in the renal excretion of acids generated through metabolism and for which there is no approved treatment.
Investigators speculate that a novel target of autoimmunity in LN that affects renal tubular potassium transport results in idiopathic hypokalemia in patients with LN.
Fanconi syndrome is a condition that affects the proximal renal tubule in the kidney and impairs the organ’s ability to reabsorb substances before they are excreted in the urine.
Chronic kidney disease (CKD) is typically associated with severe fibrosis, the exact pathogenesis of which remains unclear.