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Items: 1 to 20 of 111

1.

Trimethylaminuria: causes and diagnosis of a socially distressing condition.

Mackay RJ, McEntyre CJ, Henderson C, Lever M, George PM.

Clin Biochem Rev. 2011 Feb;32(1):33-43.

2.

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.

Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA.

J Inherit Metab Dis. 2006 Feb;29(1):162-72.

PMID:
16601883
3.

Diagnosis of suspected trimethylaminuria by NMR spectroscopy.

Podadera P, Sipahi AM, Arêas JA, Lanfer-Marquez UM.

Clin Chim Acta. 2005 Jan;351(1-2):149-54. Erratum in: Clin Chim Acta. 2005 Jul 1;357(1):88. Sipahi, Aytan M [added].

PMID:
15563884
4.

Primary Trimethylaminuria.

Phillips IR, Shephard EA.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2007 Oct 8 [updated 2015 Oct 1].

5.

[Trimethylaminuria: fish-odor syndrome].

Sela BA, Trau H, Spira A.

Harefuah. 1993 Feb 1;124(3):138-9, 183. Hebrew.

PMID:
8495879
7.

Effects of the dietary supplements, activated charcoal and copper chlorophyllin, on urinary excretion of trimethylamine in Japanese trimethylaminuria patients.

Yamazaki H, Fujieda M, Togashi M, Saito T, Preti G, Cashman JR, Kamataki T.

Life Sci. 2004 Apr 16;74(22):2739-47.

PMID:
15043988
8.

[Primary trimethylaminuria: the fish odor syndrome].

Montoya Alvarez T, Guardiola PD, Roldán JO, Elviro R, Wevers R, Guijarro G.

Endocrinol Nutr. 2009 Jun-Jul;56(6):337-40. doi: 10.1016/S1575-0922(09)71948-5. Spanish.

PMID:
19695515
9.

FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor.

D'Angelo R, Esposito T, Calabrò M, Rinaldi C, Robledo R, Varriale B, Sidoti A.

Gene. 2013 Feb 25;515(2):410-5. doi: 10.1016/j.gene.2012.12.047. Epub 2012 Dec 21.

PMID:
23266626
10.
11.

A genetic polymorphism of the N-oxidation of trimethylamine in humans.

Al-Waiz M, Ayesh R, Mitchell SC, Idle JR, Smith RL.

Clin Pharmacol Ther. 1987 Nov;42(5):588-94.

PMID:
3677545
12.

Trimethylaminuria: the detection of carriers using a trimethylamine load test.

al-Waiz M, Ayesh R, Mitchell SC, Idle JR, Smith RL.

J Inherit Metab Dis. 1989;12(1):80-5.

PMID:
2501587
13.

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.

Curr Drug Metab. 2003 Apr;4(2):151-70. Review.

PMID:
12678693
14.

Trimethylamine N-oxidation in Turkish women with bacterial vaginosis.

Sardas S, Akyol D, Green RL, Mellon T, Gökmen O, Cholerton S.

Pharmacogenetics. 1996 Oct;6(5):459-63.

PMID:
8946478
15.

Trimethylaminuria.

Brewster MA, Schedewie H.

Ann Clin Lab Sci. 1983 Jan-Feb;13(1):20-4.

PMID:
6838148
16.

Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Hsu WY, Lo WY, Lai CC, Tsai FJ, Tsai CH, Tsai Y, Lin WD, Chao MC.

Rapid Commun Mass Spectrom. 2007;21(12):1915-9.

PMID:
17510942
17.

Disclosure of the metabolic retroversion of trimethylamine N-oxide in humans: a pharmacogenetic approach.

Al-Waiz M, Ayesh R, Mitchell SC, Idle JR, Smith RL.

Clin Pharmacol Ther. 1987 Dec;42(6):608-12.

PMID:
3690938
18.

A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene.

Teresa E, Lonardo F, Fiumara A, Lombardi C, Russo P, Zuppi C, Scarano G, Musumeci S, Gianfrancesco F.

Mol Genet Metab. 2006 Jun;88(2):192-5. Epub 2006 Apr 4.

PMID:
16600650
19.

Trimethylamine: metabolic, pharmacokinetic and safety aspects.

Bain MA, Fornasini G, Evans AM.

Curr Drug Metab. 2005 Jun;6(3):227-40. Review.

PMID:
15975041
20.
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