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flumazenil and Kidney Tubular Transport, Inborn Error

flumazenil has been researched along with Kidney Tubular Transport, Inborn Error in 3 studies

Flumazenil: A potent benzodiazepine receptor antagonist. Since it reverses the sedative and other actions of benzodiazepines, it has been suggested as an antidote to benzodiazepine overdoses.
flumazenil : An organic heterotricyclic compound that is 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted at positions 3, 5, 6, and 8 by ethoxycarbonyl, methyl, oxo, and fluoro groups, respectively. It is used as an antidote to benzodiazepine overdose.

Research Excerpts

ExcerptRelevanceReference
"Renal hypouricemia (RHUC) is a heterogeneous inherited disorder characterized by impaired tubular uric acid (UA) transport with severe complications, such as acute kidney injury (AKI)."3.79Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis. ( Hulkova, H; Ichida, K; Jahnova, H; Krylov, V; Kryspinova, L; Nakamura, M; Sebesta, I; Stiburkova, B, 2013)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gabrikova, D2
Bernasovska, J1
Sokolova, J1
Stiburkova, B3
Čepek, P1
Šimek, P1
Kristian, P1
Cordoba-Lanus, E1
Claverie-Martin, F1
Sebesta, I1
Ichida, K1
Nakamura, M1
Hulkova, H1
Krylov, V1
Kryspinova, L1
Jahnova, H1

Other Studies

3 other studies available for flumazenil and Kidney Tubular Transport, Inborn Error

ArticleYear
High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction.
    Urolithiasis, 2015, Volume: 43, Issue:5

    Topics: Czech Republic; Genetic Testing; Humans; Organic Anion Transporters; Organic Cation Transport Protei

2015
Prevalence of URAT1 allelic variants in the Roma population.
    Nucleosides, nucleotides & nucleic acids, 2016, Volume: 35, Issue:10-12

    Topics: Evolution, Molecular; Female; Founder Effect; Gene Frequency; Genetic Association Studies; Heterozyg

2016
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.
    European journal of human genetics : EJHG, 2013, Volume: 21, Issue:10

    Topics: Absorption; Acute Kidney Injury; Adult; Alleles; Animals; Child; Czech Republic; Endoplasmic Reticul

2013