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.
Excerpt | Relevance | Reference |
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"HMSNR affects only patients with Roma origin, similar to the better known HMSN type Lom clarified earlier." | 1.43 | HSMNR 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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gabrikova, D | 1 |
Mistrik, M | 1 |
Bernasovska, J | 1 |
Bozikova, A | 1 |
Behulova, R | 1 |
Tothova, I | 1 |
Macekova, S | 1 |
Šafka Brožková, D | 2 |
Haberlová, J | 1 |
Mazanec, R | 1 |
Laštůvková, J | 1 |
Seeman, P | 2 |
Paulasová Schwabová, J | 1 |
Neupauerová, J | 1 |
Sabová, J | 1 |
Krůtová, M | 1 |
Peřina, V | 1 |
Trková, M | 1 |
Laššuthová, P | 1 |
3 other studies available for flumazenil and Adult Refsum Disease
Article | Year |
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Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
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.
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.
Topics: Adult; Age of Onset; Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Chro | 2017 |