Distal Renal Tubular Acidosis

Known as: Renal tubular acidosis, distal, RTAs, Gradient Type, RENAL TUBULAR ACIDOSIS DISTAL <TYPE 1> 
The genetic defect is in the anion exchange protein gene SLC4A1 resulting in impaired excretion of hydrogen ions or renal acids in the distal renal… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1972-2018
0204019722018

Papers overview

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2007
2007
To define the renal tissue changes in stone-forming patients with distal renal tubular acidosis (dRTA), we performed intra… (More)
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Highly Cited
2004
Highly Cited
2004
While macro- and microscopic kidney development appear to proceed normally in mice that lack Foxi1, electron microscopy reveals… (More)
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Highly Cited
2002
Highly Cited
2002
Autosomal recessive distal renal tubular acidosis (rdRTA) is characterised by severe hyperchloraemic metabolic acidosis in… (More)
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Highly Cited
2000
Highly Cited
2000
The multi-subunit H+-ATPase pump is present at particularly high density on the apical (luminal) surface of α-intercalated cells… (More)
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2000
2000
Absence of band 3, associated with the mutation Coimbra (V488M) in the homozygous state, caused severe hereditary spherocytosis… (More)
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Highly Cited
1999
Highly Cited
1999
H+-ATPases are ubiquitous in nature; V-ATPases pump protons against an electrochemical gradient, whereas F-ATPases reverse the… (More)
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1999
1999
BACKGROUND A defect in the anion exchanger 1 (AE1) of the basolateral membrane of type A intercalated cells in the renal… (More)
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Highly Cited
1997
Highly Cited
1997
All affected patients in four families with autosomal dominant familial renal tubular acidosis (dRTA) were heterozygous for… (More)
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1981
1981
We studied renal function in 13 patients with obstructive uropathy and hyperkalemic metabolic acidosis to characterize the… (More)
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1978
1978
Since hypocitraturia in distal renal tubular acidosis, we screened the asymptomatic children in three families with familial dRTA… (More)
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