Results 171 to 180 of about 19,301 (213)

Inherited renal tubular acidosis

Current Opinion in Nephrology and Hypertension, 2000
The past few years have witnessed great progress in elucidating the molecular basis of inherited renal tubular acidosis. Consistent with the physiologically defined importance of multiple gene products in urinary acidification, heritable renal tubular acidosis is genetically heterogeneous.
C, Shayakul, S L, Alper
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Renal Tubular Acidosis in Leprosy

Annals of Internal Medicine, 1971
Excerpt To the editor: Dr. Talal's comments regarding the relationship of renal tubular acidosis to peritubular infiltration of lymphocytes (1) are of particular interest to us because of studies w...
D J, Drutz, R A, Gutman
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FAMILIAL RENAL TUBULAR ACIDOSIS

Annals of Internal Medicine, 1968
Excerpt To the Editor:I was interested to read the editorial note on familial renal tubular acidosis (RTA) by Dr. Vardaman M. Buckalew (Ann. Intern. Med. 68: 1367, 1968).
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Evaluation of renal tubular acidosis

The Indian Journal of Pediatrics, 2007
Renal tubular acidoses (RTA) comprises of a group of disorders characterized by a low capacity for net acid excretion and persistent hyperchloremic, metabolic acidosis. The RTAs are classified into chiefly three types (types 1,2 and 4) based on clinical and laboratory characteristics.
Arvind, Bagga, Aditi, Sinha
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Inherited tubular renal acidosis

Annales de biologie clinique, 2011
Renal tubular acidosis (RTA) is a tubulopathy characterized by metabolic acidosis with normal anion gap secondary to abnormalities of renal acidification. RTA can be classified into four main subtypes: distal RTA, proximal RTA, combined proximal and distal RTA, and hyperkalemic RTA.
Hassan, Bouzidi, Donia, Hayek, Dhekra, Nasr, Michel, Daudon, Mohamed, Fadhel Najjar   +4 more
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Renal Tubular Acidosis

New England Journal of Medicine, 1981
O M, Wrong, T G, Feest
  +7 more sources

Understanding renal tubular acidosis

British Journal of Hospital Medicine
Renal tubular acidosis is a group of disorders characterised by metabolic acidosis, hyperchloraemia, normal anion gap, and potassium imbalance. Genetic mutations, drugs or acquired disorders disrupt the function of various transport proteins and enzymes in the renal tubules, causing diminished bicarbonate reabsorption or inability to excrete hydrogen ...
Samuel Sherng Young, Wang, Haoming, Tang, Wen Qi Jane, Ho, Sharen, Asif, Yi Xin, Li, Adel, Ekladious, Muhammad M, Javaid   +6 more
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Nephrolithiasis in Renal Tubular Acidosis

Journal of Urology, 1989
Renal tubular acidosis is a term applied to several conditions in which metabolic acidosis is caused by specific defects in renal tubular hydrogen ion secretion. Three types of renal tubular acidosis generally are recognized based on the nature of the tubular defect. Nephrolithiasis occurs only in type I renal tubular acidosis, a condition marked by an
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Renal Tubular Acidosis

Annual Review of Medicine, 1978
F J, Gennari, J J, Cohen
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Familial renal tubular acidosis

Journal of Nephrology, 2010
Abstract The kidney maintains systemic acid–base homeostasis through proximal tubular reclamation of filtered bicar bonate, and excretion of the daily mineral acid load by collecting duct type A intercalated cells. Impairment of either process produces renal tubular acidosis (RTA).
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