flumazenil has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 13 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) |
| "Sensorineural hearing loss was confirmed on electrocochleography and brainstem evoked potentials." | 1.35 | Hereditary motor and sensory neuropathy Lom type in a Serbian family. ( Apostolski, S; Dacković, J; Keckarević-Marković, M; Komazec, Z; Lavrnić, D; Rakocević-Stojanović, V; Ribarić, K; Romac, S; Stević, Z, 2008) |
| "We describe a form of hereditary motor and sensory neuropathy (HMSN) affecting four siblings in an Italian family of Gypsy ethnic origin with both clinical and pathological findings very reminiscent of the HMSN Lom type (HMSNL), recently described in a group of Bulgarian Gypsies." | 1.30 | Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family. ( Kalaydjieva, L; Malandrini, A; Maraldi, NM; Merlini, L; Sabatelli, P; Trogu, A; Villanova, M; Yanakiev, P, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (23.08) | 18.2507 |
| 2000's | 6 (46.15) | 29.6817 |
| 2010's | 4 (30.77) | 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 | 1 |
| Haberlová, J | 1 |
| Mazanec, R | 1 |
| Laštůvková, J | 1 |
| Seeman, P | 1 |
| Herczegfalvi, A | 1 |
| Pikó, H | 1 |
| Karcagi, V | 1 |
| Dacković, J | 1 |
| Keckarević-Marković, M | 1 |
| Komazec, Z | 1 |
| Rakocević-Stojanović, V | 1 |
| Lavrnić, D | 1 |
| Stević, Z | 1 |
| Ribarić, K | 1 |
| Romac, S | 1 |
| Apostolski, S | 1 |
| Sevilla, T | 1 |
| Martínez-Rubio, D | 1 |
| Márquez, C | 1 |
| Paradas, C | 1 |
| Colomer, J | 3 |
| Jaijo, T | 1 |
| Millán, JM | 1 |
| Palau, F | 1 |
| Espinós, C | 1 |
| Szabó, A | 1 |
| Siska, E | 1 |
| Molnár, MJ | 1 |
| Kalaydjieva, L | 5 |
| Hallmayer, J | 1 |
| Chandler, D | 2 |
| Savov, A | 2 |
| Nikolova, A | 2 |
| Angelicheva, D | 4 |
| King, RH | 3 |
| Ishpekova, B | 2 |
| Honeyman, K | 1 |
| Calafell, F | 1 |
| Shmarov, A | 2 |
| Petrova, J | 1 |
| Turnev, I | 1 |
| Hristova, A | 1 |
| Moskov, M | 1 |
| Stancheva, S | 1 |
| Petkova, I | 1 |
| Bittles, AH | 1 |
| Georgieva, V | 1 |
| Middleton, L | 1 |
| Thomas, PK | 3 |
| Merlini, L | 3 |
| Villanova, M | 1 |
| Sabatelli, P | 1 |
| Trogu, A | 1 |
| Malandrini, A | 1 |
| Yanakiev, P | 2 |
| Maraldi, NM | 1 |
| Butinar, D | 3 |
| Zidar, J | 2 |
| Leonardis, L | 2 |
| Popovic, M | 2 |
| Sininger, Y | 1 |
| Keats, B | 2 |
| Starr, A | 2 |
| Timmerman, V | 1 |
| Löfgren, A | 1 |
| Van Broeckhoven, C | 1 |
| Heather, L | 1 |
| Gooding, R | 1 |
| Gresham, D | 1 |
| de Jonge, R | 1 |
| Baas, F | 1 |
| Dye, D | 1 |
| Karagyozov, L | 1 |
| Blechschmidt, K | 1 |
| Tournev, I | 2 |
| Urtizberea, JA | 1 |
| Chabrol, B | 1 |
| Voit, T | 1 |
| Baethmann, M | 1 |
| Nedkova, V | 1 |
| Corches, A | 2 |
| Youl, B | 1 |
| Rogers, T | 1 |
| Guergueltcheva, V | 1 |
| Lupu, C | 1 |
| Popa, G | 1 |
| Muddle, JR | 1 |
| Nourallah, M | 1 |
13 other studies available for flumazenil and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
| 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 |
[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 |
Hereditary motor and sensory neuropathy Lom type in a Serbian family.
Topics: Adult; Cochlear Nerve; Female; Hearing Loss, Sensorineural; Hereditary Sensory and Motor Neuropathy; | 2008 |
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 |
[Hereditary motor and sensory Lom-neuropathy--first Hungarian case report].
Topics: Adolescent; Adult; Cell Cycle Proteins; Child; Chromosomes, Human, Pair 8; Female; Hereditary Sensor | 2007 |
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
Topics: Adolescent; Bulgaria; Child; Chromosome Mapping; Chromosomes, Human, Pair 8; Female; Founder Effect; | 1996 |
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family.
Topics: Adolescent; Child; Chromosomes, Human, Pair 8; Conserved Sequence; Genetic Linkage; Haplotypes; Here | 1998 |
Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
Topics: Acoustic Stimulation; Adult; Chromosomes, Human, Pair 8; Evoked Potentials, Auditory, Brain Stem; Ge | 1999 |
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
Topics: Adolescent; Adult; Child, Preschool; Cochlear Nerve; Cranial Nerve Diseases; Electromyography; Elect | 2000 |
Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries.
Topics: Adolescent; Adult; Child; Chromosome Mapping; Disease Progression; DNA Mutational Analysis; Europe; | 2000 |
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
Topics: Adolescent; Adult; Biopsy; Bulgaria; Child; Chromosome Mapping; Chromosomes, Human, Pair 10; Family | 2001 |