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References in periodicals archive ?
Percentages were calculated for various metabolic risks factors as hypercalciuria, hyperoxaluria, hypocitraturia and renal tubular acidosis were detected from laboratory work up.
Elkinton, "Incomplete renal tubular acidosis. Physiologic studies in three patients with a defect in lowering urine pH," The American Journal of Medicine, vol.
Although the lactate level increased during the surgery, this cannot be explained by increased production as no haemodynamic instability was recorded but may be related to impaired excretion of lactate as a part of renal tubular acidosis.
An unusual initial presentation of Sjogren's syndrome: severe hypokalemic paralysis secondary to distal renal tubular acidosis. Eurasian J Med 2013;45:218-21.
Tu et al., "Clinical analysis of hyperkalemic renal tubular acidosis caused by calcineurin inhibitors in solid organ transplant recipients," Journal of Clinical Pharmacy and Therapeutics, vol.
Sasaki, "Sjogren's syndrome and renal tubular acidosis," The American Journal of Medicine, vol.
In the incomplete renal tubular acidosis kidney is unable to acidify urine to a pH lower than 5.0, wherein direct/complete renal tubular acidosis kidney has very little capacity for acidification with result that alkaline urine is excreted.
"Unfortunately it was and she was diagnosed with a very rare condition called Renal Tubular Acidosis Type 4.
Thyrotoxicosis and renal tubular acidosis presenting as hypokalaemic paralysis.
Cancer accounted for 9.2 per cent of deaths last year followed by hypertension (7.2 per cent); Ischemic Heart Disease (3.7 per cent); Renal Tubular Acidosis (RTA), a medical condition involving accumulation of acid in the body due to kidney failure (3.4 per cent); strokes (2.7 per cent); renal failure (2.3 per cent); sickle cell disease (1.3 per cent) and pneumonia (1.1 per cent).
Cystine stones frequently have a smooth edged, ground-glass appearance.3 Cystinuria is an autosomal recessive disorder and distal renal tubular acidosis may be transmitted as a hereditary trait, thus urolithiasis occurs in up to 75% of patients affected with this disorder.11 Radiographically cystine stones appear lightly opaque (due to the sulphur content) with homogeneous density, typically a "groundglass" appearance.
Carbonic anhydrase II deficiency syndrome: Recessive osteopetrosis with renal tubular acidosis and cerebral calcification.