flumazenil has been researched along with Congenital Myasthenia 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 |
|---|---|---|
| "Mutations in its gene may cause congenital myasthenic syndromes." | 1.30 | A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. ( Abicht, A; Brunner, J; Herczegfalvi, A; Horváth, R; Janssen, G; Jost, W; Karcagi, V; Lochmüller, H; Mortier, W; Müller-Felber, W; Pongratz, D; Ramaekers, V; Rüdel, R; Schara, U; Schlotter, B; Seidel, U; Stucka, R, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Urtizberea, JA | 1 |
| Lochmuller, H | 2 |
| Tournev, I | 1 |
| Natera-de Benito, D | 1 |
| Domínguez-Carral, J | 1 |
| Muelas, N | 1 |
| Nascimento, A | 1 |
| Ortez, C | 1 |
| Jaijo, T | 1 |
| Arteaga, R | 1 |
| Colomer, J | 1 |
| Vilchez, JJ | 1 |
| Abicht, A | 1 |
| Stucka, R | 1 |
| Karcagi, V | 1 |
| Herczegfalvi, A | 1 |
| Horváth, R | 1 |
| Mortier, W | 1 |
| Schara, U | 1 |
| Ramaekers, V | 1 |
| Jost, W | 1 |
| Brunner, J | 1 |
| Janssen, G | 1 |
| Seidel, U | 1 |
| Schlotter, B | 1 |
| Müller-Felber, W | 1 |
| Pongratz, D | 1 |
| Rüdel, R | 1 |
3 other studies available for flumazenil and Congenital Myasthenia
| Article | Year |
|---|---|
[Myology and ethnic minorities: all roads lead to the Roma].
Topics: Bulgaria; Congresses as Topic; Consanguinity; Culture; Ethnicity; Founder Effect; France; History, 1 | 2015 |
Phenotypic heterogeneity in two large Roma families with a congenital myasthenic syndrome due to CHRNE 1267delG mutation. A long-term follow-up.
Topics: Adolescent; Adult; Child; Family; Female; Follow-Up Studies; Humans; Male; Middle Aged; Mutation; My | 2016 |
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.
Topics: Adolescent; Adult; Child; Child, Preschool; Europe; Female; Genotype; Homozygote; Humans; Infant; Ma | 1999 |