flumazenil has been researched along with Abnormalities, Multiple in 9 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.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| 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 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 | 3 (33.33) | 18.7374 |
| 1990's | 4 (44.44) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Siccha, SM | 1 |
| Cueto, AM | 1 |
| Parrón-Pajares, M | 1 |
| González-Morán, G | 1 |
| Pacio-Miguez, M | 1 |
| Del Pozo, Á | 1 |
| Solís, M | 1 |
| Rodriguez-Jimenez, C | 1 |
| Caino, S | 1 |
| Fano, V | 1 |
| Heath, KE | 1 |
| García-Miñaúr, S | 1 |
| Palomares-Bralo, M | 1 |
| Santos-Simarro, F | 1 |
| Kalaydjieva, L | 1 |
| Malpuech, G | 1 |
| Demeocq, F | 1 |
| Palcoux, JB | 1 |
| Vanlieferinghen, P | 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 |
| López de la Torre Casares, M | 1 |
| Rodríguez Poyo-Guerrero, P | 1 |
| Gargallo Fernández, M | 1 |
| Moreno Esteban, B | 1 |
| Jara Albarrán, A | 1 |
| Forrai, G | 1 |
| Tauszik, T | 1 |
| Tauszik, N | 1 |
| Mohr, T | 1 |
| Tunyogi, MC | 1 |
| Holics, C | 1 |
| Bánkövi, G | 1 |
| Gál, I | 1 |
3 reviews available for flumazenil and Abnormalities, Multiple
| Article | Year |
|---|---|
Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literature.
Topics: Abnormalities, Multiple; Bone Diseases, Developmental; Bone Diseases, Metabolic; Child, Preschool; C | 2021 |
Congenital cataracts-facial dysmorphism-neuropathy.
Topics: Abnormalities, Multiple; Cataract; Chromosomes, Human, Pair 18; Face; Facial Nerve Diseases; Humans; | 2006 |
[Aplasia cutis congenita, epidermolysis bullosa and ungual dystrophy].
Topics: Abnormalities, Multiple; Ectodermal Dysplasia; Epidermolysis Bullosa; Humans; Infant, Newborn; Male; | 1998 |
6 other studies available for flumazenil and Abnormalities, Multiple
| Article | Year |
|---|---|
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 |
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 |
Prevalence of congenital anomaly syndromes in a Spanish gypsy population.
Topics: Abnormalities, Multiple; Albinism; Case-Control Studies; Cleft Lip; Cleft Palate; Congenital Abnorma | 1992 |
[Infantile appearance at age l6 in a girl with hypothyroidism and total situs inversus].
Topics: Abnormalities, Multiple; Adolescent; Bone Diseases, Developmental; Congenital Hypothyroidism; Growth | 1989 |
A high incidence of PKD in a large geographic area of south-western Hungary: a medical genetic study.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Chromos | 1989 |