Page last updated: 2024-10-27

flumazenil and Adult Refsum Disease

flumazenil has been researched along with Adult Refsum Disease 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
"HMSNR affects only patients with Roma origin, similar to the better known HMSN type Lom clarified earlier."1.43HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL. ( Haberlová, J; Laštůvková, J; Mazanec, R; Šafka Brožková, D; Seeman, P, 2016)

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, D1
Mistrik, M1
Bernasovska, J1
Bozikova, A1
Behulova, R1
Tothova, I1
Macekova, S1
Šafka Brožková, D2
Haberlová, J1
Mazanec, R1
Laštůvková, J1
Seeman, P2
Paulasová Schwabová, J1
Neupauerová, J1
Sabová, J1
Krůtová, M1
Peřina, V1
Trková, M1
Laššuthová, P1

Other Studies

3 other studies available for flumazenil and Adult Refsum Disease

ArticleYear
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
    Journal of applied genetics, 2013, Volume: 54, Issue:4

    Topics: Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Consanguinity; Female; Founder Effect; Genes, Rece

2013
HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL.
    Clinical genetics, 2016, Volume: 90, Issue:2

    Topics: Adolescent; Adult; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Czech Republic; Female; Fou

2016
HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 8.
    Journal of human genetics, 2017, Volume: 62, Issue:3

    Topics: Adult; Age of Onset; Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Chro

2017