Results 101 to 110 of about 624,431 (182)

Renal hypouricemia in a recipient of living-donor kidney transplantation: a case report and literature review. [PDF]

open access: yesCEN Case Rep, 2022
Miyauchi T   +11 more
europepmc   +1 more source

Evaluation of the proximal tubular function in individuals with primary renal hypouricemia: an NMR-based metabonomic study

open access: yes, 2009
Primary renal hypouricemia (PRH) refers to a rare condition of increased renal urate clearance, caused by an isolated inborn error of membrane transport of urate in the renal proximal tubule.
Elisaf, M. S.   +4 more
core  

Prevalence and clinical significance of hypouricemia in the emergency department [PDF]

open access: yes
Hypouricemia prevalence has been reported in different clinical settings, but its prevalence and characteristics in the emergency department (ED) are limitedly studied.
Selki, Kudret   +2 more
core   +1 more source

Renal Hypouricemia with Exercise Induced Acute Kidney Injury-A Case Report. [PDF]

open access: yesIndian J Nephrol, 2021
Gundlapalli S   +4 more
europepmc   +1 more source

A Proposal for Practical Diagnosis of Renal Hypouricemia: Evidenced from Genetic Studies of Nonfunctional Variants of URAT1/SLC22A12 among 30,685 Japanese Individuals. [PDF]

open access: yesBiomedicines, 2021
Kawamura Y   +25 more
europepmc   +1 more source

Renal hypouricemia

open access: yes
Research HypothesisOur hypothesis is that novel mutations in the SLC2A9 gene, particularly the newly identified c.1004T>A mutation, contribute to recurrent episodes of exercise-induced acute kidney injury (EIAKI) even under low-intensity physical ...
Vukkadala, M (via Mendeley Data)
core   +1 more source

ASYMPTOMATIC HYPOURICEMIA: A CLINICAL CASE [PDF]

open access: yes
Hypouricemia is a sporadic problem in medicine and is mentioned for relationship to some clinical disorders. Here, the authors report a case of hypouricemia in asymptomatic patient. The positive findings in this patient are high fasting blood glucose and
YASRI, SORA
core  

Hereditary renal hypouricemia with SLC22A12 mutation: A case report

open access: yesPediatrics and Neonatology, 2022
Jisook Yim, Myungshin Kim, Jin-Soon Suh
doaj   +1 more source

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