flumazenil has been researched along with Cataract 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.
Cataract: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Management includes surgical treatment of the cataracts, and rehabilitation and corrective orthopaedic surgery for the peripheral neuropathy." | 2.43 | Congenital cataracts-facial dysmorphism-neuropathy. ( Kalaydjieva, L, 2006) |
| "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) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 7 (70.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haret, D | 1 |
| Lassuthova, P | 1 |
| Sišková, D | 1 |
| Haberlová, J | 1 |
| Sakmaryová, I | 1 |
| Filouš, A | 1 |
| Seeman, P | 1 |
| Herczegfalvi, A | 1 |
| Pikó, H | 1 |
| Karcagi, V | 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 |
| Angelicheva, D | 3 |
| Yong, KK | 1 |
| Ambrugger, P | 1 |
| Reinhold, A | 1 |
| Morar, B | 1 |
| Baas, F | 1 |
| Kwa, M | 1 |
| Tournev, I | 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 |
| Kalaydjieva, L | 4 |
| 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 |
| Turnev, I | 1 |
| Dye, D | 1 |
| Chandler, D | 1 |
| Müller-Felber, W | 1 |
| Walter, MC | 1 |
| Talim, B | 1 |
| Hallmayer, J | 1 |
1 review available for flumazenil and Cataract
| Article | Year |
|---|---|
Congenital cataracts-facial dysmorphism-neuropathy.
Topics: Abnormalities, Multiple; Cataract; Chromosomes, Human, Pair 18; Face; Facial Nerve Diseases; Humans; | 2006 |
9 other studies available for flumazenil and Cataract
| Article | Year |
|---|---|
Rectal Flumazenil can save the day.
Topics: Administration, Rectal; Anesthesia Recovery Period; Anti-Anxiety Agents; Antidotes; Cataract; Catara | 2008 |
Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech Gypsy children--frequent and underestimated cause of disability among Czech Gypsies.
Topics: Adolescent; Cataract; Child; Child, Preschool; Craniofacial Abnormalities; Czech Republic; Female; H | 2014 |
[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 |
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 |
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 |
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 |