Page last updated: 2024-10-27

flumazenil and Limb-Girdle Muscular Dystrophies

flumazenil has been researched along with Limb-Girdle Muscular Dystrophies 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.

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Justel, M1
Jou, C1
Sariego-Jamardo, A1
Juliá-Palacios, NA1
Ortez, C1
Poch, ML1
Hedrera-Fernandez, A1
Gomez-Martin, H1
Codina, A1
Dominguez-Carral, J1
Muxart, J1
Hernández-Laín, A1
Vila-Bedmar, S1
Zulaica, M1
Cancho-Candela, R1
Castro, MDC1
de la Osa-Langreo, A1
Peña-Valenceja, A1
Marcos-Vadillo, E1
Prieto-Matos, P1
Pascual-Pascual, SI1
López de Munain, A1
Camacho, A1
Estevez-Arias, B1
Musokhranova, U1
Olivella, M1
Oyarzábal, A1
Jimenez-Mallebrera, C1
Domínguez-González, C1
Nascimento, A1
García-Cazorla, À1
Natera-de Benito, D1
Mavillard, F1
Madruga-Garrido, M1
Rivas, E1
Servián-Morilla, E1
Ávila-Polo, R1
Marcos, I1
Morón, FJ1
Paradas, C1
Cabrera-Serrano, M1
Herczegfalvi, A1
Pikó, H1
Karcagi, V1
Aranka, L1
Peter, M1
Jeno, K1
Katalin, R1
Gyula, T1
Emoke, E1
Agnes, H1
Tibor, H1
Laszlo, T1
Edit, B1
Marta, K1
Janos, S1
Veronika, K1
Spengos, K1
Walter, MC1
Dekomien, G1
Papadopoulos, K1
Lochmüller, H1
Manta, P1
Georgieva, B1
Todorova, A1
Tournev, I1
Mitev, V1
Kremensky, I1

Other Studies

6 other studies available for flumazenil and Limb-Girdle Muscular Dystrophies

ArticleYear
Expanding the phenotypic spectrum of
    Journal of medical genetics, 2023, Volume: 60, Issue:10

    Topics: Humans; Intellectual Disability; Microcephaly; Muscle Weakness; Muscular Dystrophies; Muscular Dystr

2023
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay.
    Annals of clinical and translational neurology, 2019, Volume: 6, Issue:11

    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].
    Ideggyogyaszati szemle, 2008, Nov-30, Volume: 61, Issue:11-12

    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.
    Ideggyogyaszati szemle, 2009, Jan-30, Volume: 62, Issue:1-2

    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.
    European journal of neurology, 2010, Jun-01, Volume: 17, Issue:6

    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.
    Clinical genetics, 2004, Volume: 66, Issue:5

    Topics: Bulgaria; Female; Genetic Carrier Screening; Genetic Testing; Genetics, Population; Humans; Infant,

2004