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Renal hypouricemia

Known as: Dalmatian hypouricemia, Hypouricemia, renal, Hypouricemia, Renal, 1 
National Institutes of Health

Related topics

Related topics

8 relations
Autosomal recessive inheritanceHypouricemiaSLC22A12, GLU298ASPSLC22A12, THR217MET

Broader (2)

Renal Tubular Transport, Inborn ErrorsUrinary Calculi

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Clinical practice guideline for renal hypouricemia (1st edition)
Renal hypouricemia (RHUC) is a disease caused by dysfunction of renal urate reabsorption transporters; however, diagnostic… 
Highly Cited
2010
Highly Cited
2010
Homozygous SLC2A9 mutations cause severe renal hypouricemia.
Hereditary hypouricemia may result from mutations in the renal tubular uric acid transporter URAT1. Whether mutation of other… 
Highly Cited
2008
Highly Cited
2008
Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia.
Highly Cited
2008
Highly Cited
2008
Field‐based competitive impacts between invaders and natives at varying resource supply
1 One line of thinking is that highly successful plant invaders achieve dominance in recipient communities via competitive… 
Highly Cited
2007
Highly Cited
2007
Canine Dal blood type: A red cell antigen lacking in some Dalmatians.
BACKGROUND Based upon alloantibodies produced after sensitizing dogs with transfused blood, more than a dozen blood group systems… 
Highly Cited
2005
Highly Cited
2005
Acute renal failure due to uric acid nephropathy in a patient with renal hypouricemia
SummaryThis report is about a 23-year-old man who required hemodialysis in connection with an acute renal failure resulting from… 
2005
2005
Recurrent URAT1 gene mutations and prevalence of renal hypouricemia in Japanese
Recent identification of the urate transporter in the kidney (URAT1, encoded by SLC22A12) led to the molecular elucidation of… 
Highly Cited
2004
Highly Cited
2004
Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion.
Renal hypouricemia is an inherited and heterogeneous disorder characterized by increased urate clearance (CUA). The authors… 
Highly Cited
2004
Highly Cited
2004
A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese.
BACKGROUND Recently, SLC22A12 has been identified as a urate-anion exchanger in the human kidney. METHODS We screened for… 
Review
2002
Review
2002
Acute Renal Failure with Severe Loin Pain and Patchy Renal Ischemia after Anaerobic Exercise in Patients with or without Renal Hypouricemia
Acute renal failure induced by rhabdomyolysis after strenuous exercise is well known. We describe here a new type of acute renal… 
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