flumazenil has been researched along with Muscular Dystrophies, Limb-Girdle in 6 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.
Muscular Dystrophies, Limb-Girdle: A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Justel, M | 1 |
| Jou, C | 1 |
| Sariego-Jamardo, A | 1 |
| Juliá-Palacios, NA | 1 |
| Ortez, C | 1 |
| Poch, ML | 1 |
| Hedrera-Fernandez, A | 1 |
| Gomez-Martin, H | 1 |
| Codina, A | 1 |
| Dominguez-Carral, J | 1 |
| Muxart, J | 1 |
| Hernández-Laín, A | 1 |
| Vila-Bedmar, S | 1 |
| Zulaica, M | 1 |
| Cancho-Candela, R | 1 |
| Castro, MDC | 1 |
| de la Osa-Langreo, A | 1 |
| Peña-Valenceja, A | 1 |
| Marcos-Vadillo, E | 1 |
| Prieto-Matos, P | 1 |
| Pascual-Pascual, SI | 1 |
| López de Munain, A | 1 |
| Camacho, A | 1 |
| Estevez-Arias, B | 1 |
| Musokhranova, U | 1 |
| Olivella, M | 1 |
| Oyarzábal, A | 1 |
| Jimenez-Mallebrera, C | 1 |
| Domínguez-González, C | 1 |
| Nascimento, A | 1 |
| García-Cazorla, À | 1 |
| Natera-de Benito, D | 1 |
| Mavillard, F | 1 |
| Madruga-Garrido, M | 1 |
| Rivas, E | 1 |
| Servián-Morilla, E | 1 |
| Ávila-Polo, R | 1 |
| Marcos, I | 1 |
| Morón, FJ | 1 |
| Paradas, C | 1 |
| Cabrera-Serrano, M | 1 |
| Herczegfalvi, A | 1 |
| Pikó, H | 1 |
| Karcagi, V | 1 |
| Aranka, L | 1 |
| Peter, M | 1 |
| Jeno, K | 1 |
| Katalin, R | 1 |
| Gyula, T | 1 |
| Emoke, E | 1 |
| Agnes, H | 1 |
| Tibor, H | 1 |
| Laszlo, T | 1 |
| Edit, B | 1 |
| Marta, K | 1 |
| Janos, S | 1 |
| Veronika, K | 1 |
| Spengos, K | 1 |
| Walter, MC | 1 |
| Dekomien, G | 1 |
| Papadopoulos, K | 1 |
| Lochmüller, H | 1 |
| Manta, P | 1 |
| Georgieva, B | 1 |
| Todorova, A | 1 |
| Tournev, I | 1 |
| Mitev, V | 1 |
| Kremensky, I | 1 |
6 other studies available for flumazenil and Muscular Dystrophies, Limb-Girdle
| Article | Year |
|---|---|
Expanding the phenotypic spectrum of
Topics: Humans; Intellectual Disability; Microcephaly; Muscle Weakness; Muscular Dystrophies; Muscular Dystr | 2023 |
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay.
Topics: Adolescent; Calpain; Child; Female; Founder Effect; Humans; Introns; Male; Muscle Proteins; Muscular | 2019 |
[Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary].
Topics: Cataract; Face; Founder Effect; Frameshift Mutation; Gene Deletion; Hereditary Sensory and Motor Neu | 2008 |
Genetically determined neuromuscular disorders of some Roma families living in Hungary.
Topics: Abortion, Therapeutic; Adolescent; Adult; Age of Onset; Aged; Child; Electromyography; Female; Gene | 2009 |
C283Y mutation in the gamma-sarcoglycan gene in Greek Gypsies with severe limb girdle muscular dystrophy.
Topics: Child; Child, Preschool; Female; Founder Effect; Greece; Humans; Infant; Male; Muscular Dystrophies, | 2010 |
C283Y gamma-sarcoglycan gene mutation in the Bulgarian Roma (Gypsy) population: prevalence study and carrier screening in a high-risk community.
Topics: Bulgaria; Female; Genetic Carrier Screening; Genetic Testing; Genetics, Population; Humans; Infant, | 2004 |