Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease

• Published in: Nephrology, dialysis, transplantation Vol. 22; no. 3; pp. 807 - 812
• Main Authors: Walsh, Stephen, Turner, Clare M., Toye, Ashley, Wagner, Carsten, Jaeger, Philippe, Laing, Christopher, Unwin, Robert
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.03.2007; Oxford Publishing Limited (England)
• Subjects: Acidosis, Renal Tubular - complications; Acidosis, Renal Tubular - genetics; Acidosis, Renal Tubular - metabolism; Adult; AE1; Aged; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Anion Exchange Protein 1, Erythrocyte - genetics; Anion Exchange Protein 1, Erythrocyte - metabolism; autoimmune disease; Bicarbonates - metabolism; Biological and medical sciences; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis; DNA - genetics; Emergency and intensive care: renal failure. Dialysis management; Erythrocytes - metabolism; Female; Gene Expression; Genetic Predisposition to Disease; H+-ATPase; Humans; Immunohistochemistry; Intensive care medicine; Male; Medical sciences; Mutation; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Proton-Translocating ATPases - metabolism; renal biopsy; Renal failure; renal tubular acidosis; Sjogren's Syndrome - complications; Sjogren's Syndrome - genetics; Sjogren's Syndrome - metabolism; Sjögren's syndrome; SLC4A1; Transfusions. Complications. Transfusion reactions. Cell and gene therapy; renal tubular acidosis; Sjögren's syndrome; ATPase; renal biopsy; H; AE1; autoimmune disease; Kidney disease; Immunohistochemistry; Immunopathology; Urinary system disease; Enzyme; Stomatology; Hemodialysis; Adenosinetriphosphatase; Autoimmune disease; SLC4A1; Sjögren syndrome; Extrarenal dialysis; Eye disease; Biopsy; Systemic disease; Renal failure; Hydrolases; H+-ATPase; Mutation; Comparative study
• ISSN: 0931-0509; 1460-2385
• DOI: 10.1093/ndt/gfl662