flumazenil has been researched along with Muscular Dystrophies in 8 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: A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 1 (12.50) | 24.3611 |
| 2020's | 2 (25.00) | 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 | 2 |
| 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 | 2 |
| Servián-Morilla, E | 1 |
| Rivas, E | 2 |
| Paradas, C | 2 |
| Cabrera-Serrano, M | 2 |
| Biancalana, V | 1 |
| Morar, B | 1 |
| Olive, M | 1 |
| Muelas, N | 1 |
| Khan, E | 1 |
| Carvajal, A | 1 |
| Quiroga, P | 1 |
| Diaz-Manera, J | 1 |
| Davis, M | 1 |
| Ávila, R | 1 |
| Domínguez, C | 1 |
| Romero, NB | 1 |
| Vílchez, JJ | 1 |
| Comas, D | 1 |
| Laing, NG | 1 |
| Laporte, J | 1 |
| Kalaydjieva, L | 2 |
| Piccolo, F | 1 |
| Jeanpierre, M | 2 |
| Leturcq, F | 2 |
| Dodé, C | 1 |
| Azibi, K | 1 |
| Toutain, A | 2 |
| Merlini, L | 2 |
| Jarre, L | 2 |
| Navarro, C | 3 |
| Krishnamoorthy, R | 1 |
| Tomé, FM | 1 |
| Urtizberea, JA | 1 |
| Beckmann, JS | 1 |
| Campbell, KP | 1 |
| Kaplan, JC | 2 |
| García-García, D | 1 |
| Teijeira-Bautista, S | 1 |
| Fernández-Rodríguez, JM | 1 |
| Flores-Calvete, J | 1 |
| Sánchez-Espíldora, P | 1 |
| Fernández-Couto, D | 1 |
| Cimas-Hernando, I | 1 |
| Teijeiro-Ferreira, A | 1 |
| Fernández-Hojas, R | 2 |
| Brasa-Fernández Fierros, J | 1 |
| Martínez de Alegría, A | 1 |
| Escribano-Arias, JL | 1 |
| Núñez-Delgado, M | 1 |
| Navarro-Fernández Balbuena, C | 1 |
| Todorova, A | 1 |
| Ashikov, A | 1 |
| Beltcheva, O | 1 |
| Tournev, I | 2 |
| Kremensky, I | 1 |
| Barois, A | 1 |
| Bonneau, D | 1 |
| Brasa, J | 1 |
| Echenne, B | 1 |
| Gallano, P | 1 |
| Levi-Gomes, A | 1 |
| Urtizberea, A | 1 |
| Vallat, JM | 1 |
| Voit, T | 1 |
| Warter, JM | 1 |
| Calvo, F | 1 |
| Teijeira, S | 1 |
| Fernandez, JM | 1 |
| Teijeiro, A | 1 |
| Fernandez-Lopez, XA | 1 |
| Martin, E | 1 |
8 other studies available for flumazenil and Muscular Dystrophies
| Article | Year |
|---|---|
Expanding the phenotypic spectrum of
Topics: Humans; Intellectual Disability; Microcephaly; Muscle Weakness; Muscular Dystrophies; Muscular Dystr | 2023 |
Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy.
Topics: Anoctamins; Exons; Female; Humans; Introns; Middle Aged; Muscular Dystrophies; Mutation; RNA Splice | 2021 |
A Roma founder
Topics: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Child; Cohort Studies; Founder Effect; Huma | 2018 |
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India.
Topics: Biomarkers; Cytoskeletal Proteins; Europe; Genetics, Population; Humans; India; Membrane Glycoprotei | 1996 |
[Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases].
Topics: Adolescent; Adult; Biopsy; Child; Child, Preschool; Chromosomes, Human, Pair 13; Consanguinity; Cyto | 1998 |
C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian Gypsy population.
Topics: Base Sequence; Bulgaria; Chromosomes, Human, Pair 13; Cytoskeletal Proteins; Heterozygote; Humans; M | 1999 |
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation.
Topics: Adolescent; Adult; Age of Onset; Child; Child, Preschool; Cytoskeletal Proteins; Female; Humans; Mal | 2000 |
Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients.
Topics: Adolescent; Child; DNA Mutational Analysis; Echocardiography; Electrocardiography; Electromyography; | 2000 |