flumazenil has been researched along with Atrophy, Muscular, Peroneal in 10 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 |
|---|---|---|
| "HMSNR affects only patients with Roma origin, similar to the better known HMSN type Lom clarified earlier." | 1.43 | HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL. ( Haberlová, J; Laštůvková, J; Mazanec, R; Šafka Brožková, D; Seeman, P, 2016) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (50.00) | 29.6817 |
| 2010's | 5 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gabrikova, D | 1 |
| Mistrik, M | 1 |
| Bernasovska, J | 1 |
| Bozikova, A | 1 |
| Behulova, R | 1 |
| Tothova, I | 1 |
| Macekova, S | 1 |
| Fernández-Ramos, JA | 1 |
| López-Laso, E | 1 |
| Camino-León, R | 1 |
| Gascón-Jiménez, FJ | 1 |
| Jiménez-González, MD | 1 |
| Šafka Brožková, D | 2 |
| Haberlová, J | 1 |
| Mazanec, R | 1 |
| Laštůvková, J | 1 |
| Seeman, P | 3 |
| Paulasová Schwabová, J | 1 |
| Neupauerová, J | 1 |
| Sabová, J | 1 |
| Krůtová, M | 1 |
| Peřina, V | 1 |
| Trková, M | 1 |
| Laššuthová, P | 1 |
| Sevilla, T | 2 |
| Martínez-Rubio, D | 1 |
| Márquez, C | 1 |
| Paradas, C | 1 |
| Colomer, J | 2 |
| Jaijo, T | 1 |
| Millán, JM | 2 |
| Palau, F | 2 |
| Espinós, C | 2 |
| Guergueltcheva, V | 1 |
| Tournev, I | 1 |
| Bojinova, V | 1 |
| Hantke, J | 1 |
| Litvinenko, I | 1 |
| Ishpekova, B | 1 |
| Shmarov, A | 1 |
| Petrova, J | 1 |
| Jordanova, A | 1 |
| Kalaydjieva, L | 2 |
| Gooding, R | 1 |
| Angelicheva, D | 1 |
| King, RH | 1 |
| Guillén-Navarro, E | 1 |
| Parman, Y | 1 |
| Nascimento, A | 1 |
| Conill, J | 1 |
| Echaniz-Laguna, A | 1 |
| Degos, B | 1 |
| Bonnet, C | 1 |
| Latour, P | 1 |
| Hamadouche, T | 1 |
| Lévy, N | 1 |
| Leheup, B | 1 |
| Claramunt, R | 1 |
| Lupo, V | 1 |
| Cuesta, A | 1 |
| Vílchez, JJ | 1 |
| Baránková, L | 1 |
| Sisková, D | 1 |
| Hühne, K | 1 |
| Vyhnálková, E | 1 |
| Sakmaryová, I | 1 |
| Bojar, M | 1 |
| Rautenstrauss, B | 1 |
10 other studies available for flumazenil and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
Topics: Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Consanguinity; Female; Founder Effect; Genes, Rece | 2013 |
[Experience in molecular diagnostic in hereditary neuropathies in a pediatric tertiary hospital].
Topics: Adolescent; Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Connexins; Co | 2015 |
HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL.
Topics: Adolescent; Adult; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Czech Republic; Female; Fou | 2016 |
HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 8.
Topics: Adult; Age of Onset; Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Chro | 2017 |
Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth.
Topics: Adolescent; Adult; Cell Cycle Proteins; Charcot-Marie-Tooth Disease; Child; DNA Mutational Analysis; | 2013 |
Early clinical and electrophysiologic features of the two most common autosomal recessive forms of Charcot-Marie-Tooth disease in the Roma (Gypsies).
Topics: Adolescent; Bulgaria; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Diagnosis, Differential; | 2006 |
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2.
Topics: Adolescent; Adult; Age of Onset; Charcot-Marie-Tooth Disease; Child; Child, Preschool; Female; Found | 2006 |
NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement.
Topics: Adolescent; Brain; Cell Cycle Proteins; Central Nervous System; Charcot-Marie-Tooth Disease; Deafnes | 2007 |
The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4.
Topics: Charcot-Marie-Tooth Disease; Chromosome Mapping; Chromosomes, Human, Pair 10; Chromosomes, Human, Pa | 2007 |
A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMT.
Topics: Age of Onset; Base Sequence; Charcot-Marie-Tooth Disease; Child, Preschool; Demyelinating Diseases; | 2008 |