flumazenil has been researched along with Syndrome in 23 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.
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We observed an early-onset partial epilepsy syndrome with seizure semiology strongly suggestive of temporal lobe epilepsy (TLE), with mild intellectual deficit co-occurring in a large proportion of the patients." | 1.35 | Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32. ( Angelicheva, D; Azmanov, DN; Bojinova, V; Brown, M; Carter, K; Guergueltcheva, V; Jablensky, A; Kalaydjieva, L; Kaneva, R; Mihaylova, V; Morar, B; Radionova, M; Sander, JW; Smith, SJ; Stevens, JM; Tournev, I; Zlatareva, D, 2009) |
| "The CCFDN syndrome is a complex phenotype involving multiple systems, characterized by facial dysmorphism, congenital cataracts, microcorneae, delayed early motor and intellectual development, hypogonadotrop hypogonadism, hypomyelination of the peripheral nervous system, and serious complications related to general anaesthesia." | 1.34 | [Congenital cataracts facial dysmorphism neuropathy syndrome--first Hungarian case report]. ( Molnár, MJ; Neuwirth, M; Rebecca, G; Siska, E, 2007) |
| "The etiology of the syndrome is autosomal recessive and siblings are frequently affected." | 1.30 | [Fraser syndrome: frequency in our environment and clinical-epidemiological aspects of a consecutive series of cases]. ( Ayala Garcés, A; Bermejo Sánchez, E; Calvo Celada, R; Félix, V; Hernández Ramón, F; Martínez-Frías, ML, 1998) |
| "We observed an increased prevalence of birth defects, mostly because of groups of children with patterns of multiple anomalies and with autosomal recessive syndromes." | 1.28 | Prevalence of congenital anomaly syndromes in a Spanish gypsy population. ( Bermejo, E; Martínez-Frías, ML, 1992) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (17.39) | 18.7374 |
| 1990's | 8 (34.78) | 18.2507 |
| 2000's | 7 (30.43) | 29.6817 |
| 2010's | 3 (13.04) | 24.3611 |
| 2020's | 1 (4.35) | 2.80 |
| Authors | Studies |
|---|---|
| Plazzi, G | 1 |
| Rye, D | 1 |
| Vignatelli, L | 1 |
| Riva, R | 1 |
| Lugaresi, E | 1 |
| McDonald, JW | 1 |
| Bautista, RE | 1 |
| Gutmann, DH | 1 |
| Jones, EA | 1 |
| Skolnick, P | 1 |
| Mazurova, S | 1 |
| Tesarova, M | 1 |
| Zeman, J | 1 |
| Stranecky, V | 1 |
| Hansikova, H | 1 |
| Baxova, A | 1 |
| Giertlova, M | 1 |
| Lastuvkova, J | 1 |
| Chovanova, V | 1 |
| Rusnakova, S | 1 |
| Knapkova, M | 1 |
| Minarik, G | 2 |
| Honzik, T | 1 |
| Magner, M | 1 |
| Angelicheva, D | 4 |
| Tournev, I | 3 |
| Guergueltcheva, V | 1 |
| Mihaylova, V | 1 |
| Azmanov, DN | 2 |
| Morar, B | 2 |
| Radionova, M | 2 |
| Smith, SJ | 2 |
| Zlatareva, D | 1 |
| Stevens, JM | 1 |
| Kaneva, R | 1 |
| Bojinova, V | 2 |
| Carter, K | 1 |
| Brown, M | 1 |
| Jablensky, A | 2 |
| Kalaydjieva, L | 5 |
| Sander, JW | 2 |
| Zhelyazkova, S | 1 |
| Dimova, PS | 1 |
| Florez, L | 1 |
| Mulley, J | 1 |
| Scheffer, I | 1 |
| Tzifi, F | 1 |
| Pons, R | 1 |
| Athanassaki, C | 1 |
| Poulou, M | 1 |
| Kanavakis, E | 1 |
| Varon, R | 1 |
| Gooding, R | 2 |
| Steglich, C | 1 |
| Marns, L | 1 |
| Tang, H | 1 |
| Yong, KK | 1 |
| Ambrugger, P | 1 |
| Reinhold, A | 1 |
| Baas, F | 1 |
| Kwa, M | 1 |
| Guerguelcheva, V | 1 |
| Kremensky, I | 1 |
| Lochmüller, H | 2 |
| Müllner-Eidenböck, A | 1 |
| Merlini, L | 2 |
| Neumann, L | 1 |
| Bürger, J | 1 |
| Walter, M | 1 |
| Swoboda, K | 1 |
| Thomas, PK | 2 |
| von Moers, A | 1 |
| Risch, N | 1 |
| Ferák, V | 1 |
| Feráková, E | 1 |
| Ficek, A | 1 |
| Poláková, H | 1 |
| Kádasi, L | 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 |
| Shabo, G | 1 |
| Scheffer, H | 1 |
| Cruysberg, JR | 1 |
| Lammens, M | 1 |
| Pasman, JW | 1 |
| Spruit, M | 1 |
| Willemsen, MA | 1 |
| Siska, E | 1 |
| Neuwirth, M | 1 |
| Rebecca, G | 1 |
| Molnár, MJ | 1 |
| Malpuech, G | 1 |
| Demeocq, F | 1 |
| Palcoux, JB | 1 |
| Vanlieferinghen, P | 1 |
| Dellagrammaticas, H | 1 |
| Tzaki, M | 1 |
| Kapiki, A | 1 |
| Sianidou, L | 1 |
| Philippidis, P | 1 |
| Papas, C | 1 |
| Bartsocas, C | 1 |
| Váradi, V | 1 |
| Szabó, L | 1 |
| Papp, Z | 1 |
| Martínez-Frías, ML | 3 |
| Bermejo, E | 2 |
| Sánchez Otero, T | 1 |
| Urioste, M | 1 |
| Morena, V | 1 |
| Cruz, E | 1 |
| Bermejo Sánchez, E | 1 |
| Félix, V | 1 |
| Calvo Celada, R | 1 |
| Ayala Garcés, A | 1 |
| Hernández Ramón, F | 1 |
| Vázquez López, ME | 1 |
| Fernandez Díaz, ML | 1 |
| Somoza Rubio, C | 1 |
| Morales Redondo, R | 1 |
| Turnev, I | 1 |
| Dye, D | 1 |
| Chandler, D | 1 |
| Müller-Felber, W | 1 |
| Walter, MC | 1 |
| Talim, B | 1 |
| Hallmayer, J | 1 |
| Triggs, WJ | 1 |
| Beric, A | 1 |
| Butler, IJ | 1 |
| Roongta, SM | 1 |
| Bodánszky, H | 1 |
| Kelemen, J | 1 |
| Váradi, S | 1 |
| Krause, I | 1 |
2 reviews available for flumazenil and Syndrome
| Article | Year |
|---|---|
Benzodiazepine receptor ligands and the syndrome of hepatic encephalopathy.
Topics: Flumazenil; Hepatic Encephalopathy; Humans; Ligands; Receptors, GABA-A; Synaptic Transmission; Syndr | 1990 |
[Aplasia cutis congenita, epidermolysis bullosa and ungual dystrophy].
Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Epidermolysis Bullosa; Humans; Infant, Newborn; Male; | 1998 |
1 trial available for flumazenil and Syndrome
| Article | Year |
|---|---|
High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).
Topics: Child; Child, Preschool; Connexin 26; Connexins; Female; Genes, Dominant; Genetic Predisposition to | 2003 |
20 other studies available for flumazenil and Syndrome
| Article | Year |
|---|---|
Idiopathic recurrent stupor: Munchausen by proxy and medical litigation.
Topics: Benzodiazepines; Electroencephalography; Flumazenil; GABA Modulators; Humans; Italy; Malpractice; Re | 2014 |
Pseudocervical cord syndrome: a deceptive flumazenil reversible manifestation of hepatic encephalopathy.
Topics: Aged; Female; Flumazenil; Hepatic Encephalopathy; Humans; Neck; Spinal Cord Diseases; Syndrome | 1996 |
Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency.
Topics: Adolescent; Child; Child, Preschool; Czech Republic; Dentinogenesis Imperfecta; ErbB Receptors; Exom | 2020 |
Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.
Topics: Adolescent; Adult; Child; Chromosomes, Human, Pair 5; Electroencephalography; Epilepsies, Partial; E | 2009 |
Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family.
Topics: Adolescent; Alleles; Electroencephalography; Epilepsy; Follow-Up Studies; Genetic Carrier Screening; | 2010 |
Congenital cataracts, facial dysmorphism, and neuropathy syndrome.
Topics: Adult; Cataract; Face; Female; Humans; Infant, Newborn; Male; Mutation; Peripheral Nervous System Di | 2011 |
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome.
Topics: Amino Acid Sequence; Base Sequence; Binding Sites; Cataract; Chromosome Mapping; Chromosomes, Human, | 2003 |
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 |
Congenital cataract facial dysmorphism neuropathy syndrome: a clinically recognizable entity.
Topics: Cataract; Child, Preschool; Craniofacial Abnormalities; Diagnosis, Differential; Female; Humans; Neu | 2005 |
[Congenital cataracts facial dysmorphism neuropathy syndrome--first Hungarian case report].
Topics: Adolescent; Brain; Cataract; Child; Child, Preschool; Developmental Disabilities; Facial Nerve Disea | 2007 |
A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
Topics: Abnormalities, Multiple; Child; Child, Preschool; Cleft Lip; Cleft Palate; Dwarfism; Female; Genes, | 1983 |
Hanhart syndrome: possibility of autosomal recessive inheritance.
Topics: Child, Preschool; Ectromelia; Ethnicity; Genes, Recessive; Greece; Humans; Infant, Newborn; Male; Ma | 1982 |
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
Topics: Cleft Lip; Cleft Palate; Consanguinity; Female; Fingers; Humans; Hungary; Male; Pedigree; Psychomoto | 1980 |
Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia.
Topics: Abnormalities, Multiple; Eye Abnormalities; Female; Genes, Recessive; Genitalia, Female; Humans; Hyp | 1994 |
[Fraser syndrome: frequency in our environment and clinical-epidemiological aspects of a consecutive series of cases].
Topics: Abnormalities, Multiple; Eyelids; Female; Genitalia; Humans; Infant, Newborn; Male; Nose; Orbit; Rom | 1998 |
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter.
Topics: Adolescent; Adult; Cataract; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 1 | 1999 |
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.
Topics: Adolescent; Cataract; Child; Child, Preschool; Chromosomes, Human, Pair 18; Face; Female; Founder Ef | 2002 |
A congenital myasthenic syndrome refractory to acetylcholinesterase inhibitors.
Topics: Adult; Cholinesterase Inhibitors; Edrophonium; Electromyography; Female; Genes, Recessive; Humans; M | 1992 |
Prevalence of congenital anomaly syndromes in a Spanish gypsy population.
Topics: Abnormalities, Multiple; Albinism; Case-Control Studies; Cleft Lip; Cleft Palate; Congenital Abnorma | 1992 |
[Etiology, clinical picture and forensic definition of the child abuse syndrome. I].
Topics: Child Abuse; Child, Preschool; Expert Testimony; Forensic Medicine; Humans; Hungary; Male; Roma; Syn | 1988 |