trimethylamine has been researched along with Syndrome in 24 studies
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The fish odour syndrome was diagnosed in 11 subjects: the percentage of total trimethylamine excreted in their urine samples that was oxidised to trimethylamine N-oxide was < 55% under normal dietary conditions and < 25% after oral challenge with trimethylamine (in normal subjects > 80% of trimethylamine was N-oxidised)." | 5.07 | The fish odour syndrome: biochemical, familial, and clinical aspects. ( Ayesh, R; Mitchell, SC; Smith, RL; Zhang, A, 1993) |
| " The aliphatic tertiary amine, trimethylamine, is such a volatile compound that is generated to excess in patients with a metabolic disorder known as trimethylaminuria (fish-odour syndrome)." | 4.82 | Trimethylaminuria (fish-odour syndrome) and oral malodour. ( Mitchell, SC, 2005) |
| "Trimethylaminuria or fish odor syndrome is a metabolic disorder characterized by a failure in the oxidation route from trimethylamine (TMA) to trimethylamineN-oxide (TMA-O)." | 3.72 | [Primary trimethylaminuria or fish odor syndrome. A novel mutation in the first documented case in Spain]. ( Bandrés Echeverri, T; Berrade Zubiri, S; Engelke, U; Gil-Setas, A; Mazón Ramos, A; Wevers, R; Zschocke, J, 2003) |
| "Fish odour syndrome (trimethylaminuria) is a metabolic syndrome caused by abnormal excretion of trimethylamine in the breath, urine, sweat, saliva and vaginal secretions." | 3.70 | Fish odor syndrome. ( Rehman, HU, 1999) |
| "We have previously shown that primary trimethylaminuria, or fish-odour syndrome, is caused by an inherited defect in the flavin-containing monooxygenase 3 (FMO3) catalysed N-oxidation of the dietary-derived malodorous amine, trimethylamine (TMA)." | 3.70 | A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy. ( Chalmers, RA; Dolphin, CT; Holmes, HC; Iles, RA; Janmohamed, A; Michelakakis, H; Murphy, HC; Phillips, IR; Shephard, EA, 2000) |
| "An oral trimethylamine challenge test has been used to confirm the heterozygous status of patients with 'fish-odour syndrome'." | 3.69 | Fish odour syndrome: verification of carrier detection test. ( Mitchell, S; Smith, R; Zhang, AQ, 1995) |
| " Beginning with a single propositus, who had been previously diagnosed at the age of 10 as suffering from trimethylaminuria (fish-odour syndrome), both her parents and two sisters were investigated biochemically with respect to their ability to N-oxidize trimethylamine (TMA), both when derived from the diet and when administered exogenously." | 3.67 | Trimethylaminuria ('fish-odour syndrome'): a study of an affected family. ( Al-Waiz, M; Ayesh, R; Idle, JR; Mitchell, SC; Smith, RL, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (20.83) | 18.7374 |
| 1990's | 11 (45.83) | 18.2507 |
| 2000's | 8 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Almenar Bonet, MV | 1 |
| Llinares Tello, F | 1 |
| Torregrosa Quesada, ME | 1 |
| Segrelles Lloret, M | 1 |
| Mountain, H | 1 |
| Brisbane, JM | 1 |
| Hooper, AJ | 1 |
| Burnett, JR | 1 |
| Goldblatt, J | 1 |
| Mazón Ramos, A | 1 |
| Gil-Setas, A | 1 |
| Berrade Zubiri, S | 1 |
| Bandrés Echeverri, T | 1 |
| Wevers, R | 1 |
| Engelke, U | 1 |
| Zschocke, J | 2 |
| Mitchell, SC | 6 |
| Arseculeratne, G | 1 |
| Wong, AK | 1 |
| Goudie, DR | 1 |
| Ferguson, J | 1 |
| Werner, D | 1 |
| Fenwick, GR | 1 |
| Butler, EJ | 1 |
| Brewster, MA | 1 |
| Shelley, ED | 1 |
| Shelley, WB | 1 |
| Ruocco, V | 1 |
| Florio, M | 1 |
| Walker, V | 1 |
| Ayesh, R | 3 |
| Zhang, A | 2 |
| Smith, RL | 5 |
| Chen, H | 1 |
| Aiello, F | 1 |
| Zhang, AQ | 1 |
| Mitchell, S | 1 |
| Smith, R | 1 |
| Dolphin, CT | 2 |
| Janmohamed, A | 2 |
| Shephard, EA | 2 |
| Phillips, IR | 2 |
| Eugène, M | 1 |
| Kohlmueller, D | 1 |
| Quak, E | 1 |
| Meissner, T | 1 |
| Hoffmann, GF | 1 |
| Mayatepek, E | 1 |
| Rehman, HU | 1 |
| Kashyap, AS | 1 |
| Kashyap, S | 1 |
| Murphy, HC | 1 |
| Holmes, HC | 1 |
| Michelakakis, H | 1 |
| Chalmers, RA | 1 |
| Iles, RA | 1 |
| Al-Waiz, M | 2 |
| Idle, JR | 2 |
| Rothschild, JG | 1 |
| Hansen, RC | 1 |
3 reviews available for trimethylamine and Syndrome
| Article | Year |
|---|---|
Trimethylaminuria (fish-odour syndrome) and oral malodour.
Topics: Amino Acid Metabolism, Inborn Errors; Fish Products; Halitosis; Humans; Liver Diseases; Methylamines | 2005 |
Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).
Topics: Animals; Child; Choline; Chromosome Deletion; Chromosomes, Human, Pair 15; Diet; Female; Fishes; Hum | 1993 |
The fish-odor syndrome.
Topics: Diet; Halitosis; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Sweat; Syndrome | 1996 |
1 trial available for trimethylamine and Syndrome
| Article | Year |
|---|---|
The fish odour syndrome: biochemical, familial, and clinical aspects.
Topics: Adolescent; Adult; Animals; Female; Fishes; Humans; Infant; Male; Mental Disorders; Metabolism, Inbo | 1993 |
20 other studies available for trimethylamine and Syndrome
| Article | Year |
|---|---|
[Trimethylaminuria (fish-odor syndrome): a case report].
Topics: Humans; Male; Metabolic Diseases; Methylamines; Middle Aged; Odorants; Syndrome | 2008 |
Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelae.
Topics: Adult; Animals; Female; Fishes; Humans; Methylamines; Mutation; Odorants; Oxygenases; Syndrome | 2008 |
[Primary trimethylaminuria or fish odor syndrome. A novel mutation in the first documented case in Spain].
Topics: Child, Preschool; Female; Humans; Metabolic Diseases; Methylamines; Mutation; Spain; Syndrome | 2003 |
Trimethylaminuria (fish-odor syndrome): a case report.
Topics: Adult; Antioxidants; Consanguinity; Humans; Male; Metabolism, Inborn Errors; Methylamines; Mutation; | 2007 |
[Trimethylaminuria (fish-odour syndrome)--hints for a new therapeutic option with desmopressin].
Topics: Antidiuretic Agents; Child, Preschool; Deamino Arginine Vasopressin; Fish Products; Humans; Male; Me | 2007 |
Are brassica vegetables aggravating factors in trimethylaminuria (fish odour syndrome)?
Topics: Animals; Brassica; Humans; Methylamines; Odorants; Syndrome | 1983 |
The fish odor syndrome. Trimethylaminuria.
Topics: Abnormalities, Multiple; Adult; Humans; Liver; Male; Metabolic Diseases; Methylamines; Odorants; Syn | 1984 |
Fish-odor syndrome: an olfactory diagnosis.
Topics: Diet; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Sweat; Syndrome | 1995 |
The fish odour syndrome.
Topics: Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Oxidation-Reduction; Syndrome | 1993 |
Fish-odour syndrome and impaired N-oxidation.
Topics: Diet; Female; Genetic Carrier Screening; Homozygote; Humans; Male; Metal Metabolism, Inborn Errors; | 1996 |
Fish odour syndrome: verification of carrier detection test.
Topics: Adult; Female; Genetic Carrier Screening; Humans; Male; Metabolism, Inborn Errors; Methylamines; Odo | 1995 |
Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome.
Topics: Amino Acid Sequence; Animals; Base Sequence; Humans; Metabolism, Inborn Errors; Methylamines; Molecu | 1997 |
[Diagnosis of "fish odor syndrome" by urine nuclear magnetic resonance proton spectrometry].
Topics: Genetic Carrier Screening; Genetic Diseases, Inborn; Humans; Magnetic Resonance Spectroscopy; Methyl | 1998 |
Mild trimethylaminuria caused by common variants in FMO3 gene.
Topics: Adult; Child; Genes, Recessive; Genetic Variation; Humans; Metabolism, Inborn Errors; Methylamines; | 1999 |
Fish odor syndrome.
Topics: Enterobacteriaceae; Humans; Metabolic Diseases; Methylamines; Odorants; Oxidation-Reduction; Syndrom | 1999 |
Fish odour syndrome.
Topics: Alleles; Humans; Methylamines; Odorants; Oxygenases; Phenotype; Polymorphism, Genetic; Syndrome | 2000 |
A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy.
Topics: Adult; Alleles; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Child, Preschool; Femal | 2000 |
Trimethylaminuria (fish-odour syndrome): an inborn error of oxidative metabolism.
Topics: Animals; Child; Female; Fishes; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Oxidation | 1987 |
Trimethylaminuria ('fish-odour syndrome'): a study of an affected family.
Topics: Adult; Female; Humans; Male; Metabolism, Inborn Errors; Methylamines; Syndrome | 1988 |
Fish odor syndrome: trimethylaminuria with milk as chief dietary factor.
Topics: Animals; Cattle; Child; Choline; Humans; Infant; Liver; Male; Methylamines; Milk; Syndrome | 1985 |