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29 results

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Page 1
Biochemical and clinical aspects of the human flavin-containing monooxygenase form 3 (FMO3) related to trimethylaminuria.
Cashman JR, Camp K, Fakharzadeh SS, Fennessey PV, Hines RN, Mamer OA, Mitchell SC, Nguyen GP, Schlenk D, Smith RL, Tjoa SS, Williams DE, Yannicelli S. Cashman JR, et al. Curr Drug Metab. 2003 Apr;4(2):151-70. doi: 10.2174/1389200033489505. Curr Drug Metab. 2003. PMID: 12678693 Review.
Trimethylaminuria is a rare metabolic disorder that is associated with abnormal amounts of the dietary-derived trimethylamine. ...The remarkable progress in the biochemical, genetic, clinical basis for understanding the trimethylaminuria condition is summariz …
Trimethylaminuria is a rare metabolic disorder that is associated with abnormal amounts of the dietary-derived trimethylamine. ...The …
Halitosis. A common oral problem.
Spielman AI, Bivona P, Rifkin BR. Spielman AI, et al. N Y State Dent J. 1996 Dec;62(10):36-42. N Y State Dent J. 1996. PMID: 9002736 Review.
The remaining 10 percent of halitosis sufferers have systemic causes that include renal or hepatic failure, carcinomas, diabetes or trimethylaminuria. Modern analytical and microbiological techniques permit diagnosis of bad breath. ...
The remaining 10 percent of halitosis sufferers have systemic causes that include renal or hepatic failure, carcinomas, diabetes or trime …
Trimethylamine: metabolic, pharmacokinetic and safety aspects.
Bain MA, Fornasini G, Evans AM. Bain MA, et al. Curr Drug Metab. 2005 Jun;6(3):227-40. doi: 10.2174/1389200054021807. Curr Drug Metab. 2005. PMID: 15975041 Review.
Whilst the pharmacokinetics of TMA and TMNO has not been fully elucidated in humans, a number of studies provide information on the likely fate of dietary derived TMA. Trimethylaminuria is a condition that is characterized by a deficiency in FMO3 enzyme activity, resulting …
Whilst the pharmacokinetics of TMA and TMNO has not been fully elucidated in humans, a number of studies provide information on the likely f …
Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).
Chen H, Aiello F. Chen H, et al. Am J Med Genet. 1993 Feb 1;45(3):335-9. doi: 10.1002/ajmg.1320450310. Am J Med Genet. 1993. PMID: 8434620 Review.
Pathogenesis, clinical diagnosis, and management of reported cases with trimethylaminuria are reviewed. ...Amelioration of the "fish odor" by dietary choline restriction makes trimethylaminuria detection important. Association of trimethylaminuria with …
Pathogenesis, clinical diagnosis, and management of reported cases with trimethylaminuria are reviewed. ...Amelioration of the …
Archaea, specific genetic traits, and development of improved bacterial live biotherapeutic products: another face of next-generation probiotics.
Fadhlaoui K, Arnal ME, Martineau M, Camponova P, Ollivier B, O'Toole PW, Brugère JF. Fadhlaoui K, et al. Appl Microbiol Biotechnol. 2020 Jun;104(11):4705-4716. doi: 10.1007/s00253-020-10599-8. Epub 2020 Apr 12. Appl Microbiol Biotechnol. 2020. PMID: 32281023 Review.
Trimethylamine (TMA) and its oxide TMAO are important biomolecules involved in disease-associated processes in humans (e.g., trimethylaminuria and cardiovascular diseases). TMAO in plasma (pTMAO) stems from intestinal TMA, which is formed from various components of the die …
Trimethylamine (TMA) and its oxide TMAO are important biomolecules involved in disease-associated processes in humans (e.g., trimethylami …
Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: (1)H NMR spectroscopy and genetic testing.
Bouchemal N, Ouss L, Brassier A, Barbier V, Gobin S, Hubert L, de Lonlay P, Le Moyec L. Bouchemal N, et al. Orphanet J Rare Dis. 2019 Sep 18;14(1):222. doi: 10.1186/s13023-019-1174-6. Orphanet J Rare Dis. 2019. PMID: 31533761 Free PMC article.
BACKGROUND: Trimethylaminuria (TMAU) is a metabolic disorder characterized by the excessive excretion of the malodorous compound trimethylamine (TMA). ...All 11 adults presented a particular psychological or psychiatric phenotype, with a subjective perception of unpleasant …
BACKGROUND: Trimethylaminuria (TMAU) is a metabolic disorder characterized by the excessive excretion of the malodorous compound trim …
Index of suspicion.
Tarchichi T, Wong K, Fisher MM, Palomo P, Zapata F, Bawle EV. Tarchichi T, et al. Pediatr Rev. 2013 Jun;34(6):280-4. doi: 10.1542/pir.34-6-280. Pediatr Rev. 2013. PMID: 23729777
Fish odour syndrome.
Li M, Al-Sarraf A, Sinclair G, Frohlich J. Li M, et al. CMAJ. 2011 May 17;183(8):929-31. doi: 10.1503/cmaj.100642. Epub 2011 Mar 21. CMAJ. 2011. PMID: 21422137 Free PMC article. No abstract available.
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.
Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA. Chalmers RA, et al. J Inherit Metab Dis. 2006 Feb;29(1):162-72. doi: 10.1007/s10545-006-0158-6. J Inherit Metab Dis. 2006. PMID: 16601883 Clinical Trial.
Trimethylaminuria or 'fish odour syndrome' is due to excessive excretion into body fluids and breath of TMA derived from the enterobacterial metabolism of dietary precursors. The disorder is present from birth but becomes apparent as foods containing high amounts of cholin …
Trimethylaminuria or 'fish odour syndrome' is due to excessive excretion into body fluids and breath of TMA derived from the enteroba …
Primary trimethylaminuria (fish odor syndrome) and hypothyroidism in an adolescent.
Kılıç M. Kılıç M. Turk J Pediatr. 2017;59(5):614-616. doi: 10.24953/turkjped.2017.05.020. Turk J Pediatr. 2017. PMID: 29745129 Free article.
Primary trimethylaminuria (fish-odor syndrome) is a rare autosomal recessive inherited metabolic disorder due to decreased metabolism of trimethylamine by enzyme flavin-containing monooxygenase 3. ...Coexistence of primary trimethylaminuria and hypothyroidism might …
Primary trimethylaminuria (fish-odor syndrome) is a rare autosomal recessive inherited metabolic disorder due to decreased metabolism …
29 results