flumazenil has been researched along with Hearing Loss in 7 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.
Hearing Loss: A general term for the complete or partial loss of the ability to hear from one or both ears.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We evaluated the genetic etiology of hearing impairment (HI) in 15 Hungarian Roma families through exome sequencing." | 2.90 | Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. ( Acharya, A; Bene, J; Chakchouk, I; Cornejo-Sanchez, DM; Karosi, T; Leal, SM; Melegh, B; Melegh, BI; Nasir, A; Poston, A; Schrauwen, I; Szabo, Z, 2019) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Safka Brozkova, D | 1 |
| Varga, L | 2 |
| Uhrova Meszarosova, A | 1 |
| Slobodova, Z | 1 |
| Skopkova, M | 1 |
| Soltysova, A | 2 |
| Ficek, A | 2 |
| Jencik, J | 1 |
| Lastuvkova, J | 1 |
| Gasperikova, D | 2 |
| Seeman, P | 3 |
| Schrauwen, I | 1 |
| Melegh, BI | 1 |
| Chakchouk, I | 1 |
| Acharya, A | 1 |
| Nasir, A | 1 |
| Poston, A | 1 |
| Cornejo-Sanchez, DM | 1 |
| Szabo, Z | 1 |
| Karosi, T | 1 |
| Bene, J | 2 |
| Melegh, B | 3 |
| Leal, SM | 1 |
| Sipeky, C | 1 |
| Matyas, P | 2 |
| Melegh, M | 1 |
| Janicsek, I | 2 |
| Szalai, R | 1 |
| Szabo, I | 1 |
| Varnai, R | 1 |
| Tarlos, G | 1 |
| Ganczer, A | 1 |
| Mašindová, I | 1 |
| Hučková, M | 1 |
| Sůrová, M | 1 |
| Šafka-Brožková, D | 1 |
| Anwar, S | 1 |
| Straka, S | 1 |
| Ahmed, ZM | 1 |
| Profant, M | 1 |
| Klimeš, I | 1 |
| Riazuddin, S | 1 |
| Kádasi, Ľ | 1 |
| La Parra Casado, D | 1 |
| Gil González, D | 1 |
| de la Torre Esteve, M | 1 |
| Alvarez, A | 1 |
| del Castillo, I | 1 |
| Villamar, M | 1 |
| Aguirre, LA | 1 |
| González-Neira, A | 1 |
| López-Nevot, A | 1 |
| Moreno-Pelayo, MA | 1 |
| Moreno, F | 1 |
| Bouwer, S | 1 |
| Angelicheva, D | 1 |
| Chandler, D | 1 |
| Tournev, I | 1 |
| Kalaydjieva, L | 1 |
1 trial available for flumazenil and Hearing Loss
| Article | Year |
|---|---|
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma.
Topics: Amino Acid Substitution; Child; Child, Preschool; Chromosome Disorders; Female; Genes, Dominant; Gen | 2019 |
6 other studies available for flumazenil and Hearing Loss
| Article | Year |
|---|---|
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant.
Topics: beta-Mannosidosis; Czech Republic; Deafness; Ethnicity; Hearing Loss; Humans; Minority Groups; Roma; | 2020 |
Lower carrier rate of GJB2 W24X ancestral Indian mutation in Roma samples from Hungary: implication for public health intervention.
Topics: Adult; Aged; Aged, 80 and over; Connexin 26; Connexins; Female; Gene Frequency; Hearing Loss; Hetero | 2014 |
MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.
Topics: Age of Onset; Alleles; Connexin 26; Connexins; Czech Republic; Exons; Founder Effect; Gene Frequency | 2015 |
The social class gradient in health in Spain and the health status of the Spanish Roma.
Topics: Adult; Aged; Chronic Disease; Dental Caries; Disabled Persons; Female; Health Status; Health Status | 2016 |
High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss.
Topics: Chromosomes, Human, Pair 13; Codon, Nonsense; Connexin 26; Connexins; Family Health; Female; Gene Fr | 2005 |
Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolates.
Topics: Connexin 26; Connexins; Ethnicity; Genes, Recessive; Genetic Carrier Screening; Hearing Loss; Humans | 2007 |