flumazenil has been researched along with Myasthenic Syndromes, Congenital 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.
Myasthenic Syndromes, Congenital: A heterogeneous group of disorders characterized by a congenital defect in neuromuscular transmission at the NEUROMUSCULAR JUNCTION. This includes presynaptic, synaptic, and postsynaptic disorders (that are not of autoimmune origin). The majority of these diseases are caused by mutations of various subunits of the nicotinic acetylcholine receptor (RECEPTORS, NICOTINIC) on the postsynaptic surface of the junction. (From Arch Neurol 1999 Feb;56(2):163-7)
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 Myasthenic Syndromes, Congenital
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 |