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Items: 1 to 20 of 134

1.

Trimethylaminuria ('fish-odour syndrome'): a study of an affected family.

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

Clin Sci (Lond). 1988 Mar;74(3):231-6.

PMID:
3345632
2.

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
3.

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
4.

Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole.

Treacy E, Johnson D, Pitt JJ, Danks DM.

J Inherit Metab Dis. 1995;18(3):306-12.

PMID:
7474897
5.

Trimethylaminuria: the fish malodor syndrome.

Mitchell SC, Smith RL.

Drug Metab Dispos. 2001 Apr;29(4 Pt 2):517-21.

6.

The fish odour syndrome: biochemical, familial, and clinical aspects.

Ayesh R, Mitchell SC, Zhang A, Smith RL.

BMJ. 1993 Sep 11;307(6905):655-7.

7.

[Trimethylaminuria: fish-odor syndrome].

Sela BA, Trau H, Spira A.

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

PMID:
8495879
8.

Transient trimethylaminuria in childhood.

Mayatepek E, Kohlmüller D.

Acta Paediatr. 1998 Nov;87(11):1205-7.

PMID:
9846928
9.

Trimethylaminuria.

Brewster MA, Schedewie H.

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

PMID:
6838148
10.

Fish odour syndrome: verification of carrier detection test.

Zhang AQ, Mitchell S, Smith R.

J Inherit Metab Dis. 1995;18(6):669-74.

PMID:
8750603
11.

Lactulose in trimethylaminuria, the fish-odour syndrome.

Pike MG, King GS, Pettit BR, Leonard JV, Atherton DJ.

Helv Paediatr Acta. 1989 Feb;43(4):345-8.

PMID:
2708075
12.

[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
13.

Fish odor syndrome: a case report of trimethylaminuria.

Ulman CA, Trevino JJ, Miller M, Gandhi RK.

Dermatol Online J. 2014 Jan 15;20(1):21260.

14.

Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome.

Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.

Nat Genet. 1997 Dec;17(4):491-4.

PMID:
9398858
15.

Stop codon mutations in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population.

Yamazaki H, Fujita H, Gunji T, Zhang J, Kamataki T, Cashman JR, Shimizu M.

Mol Genet Metab. 2007 Jan;90(1):58-63. Epub 2006 Sep 25.

PMID:
16996766
16.

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
17.

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
18.

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
19.

Compound heterozygosity for missense mutations in the flavin-containing monooxygenase 3 (FM03) gene in patients with fish-odour syndrome.

Dolphin CT, Janmohamed A, Smith RL, Shephard EA, Phillips IR.

Pharmacogenetics. 2000 Dec;10(9):799-807.

PMID:
11191884
20.

Trimethylaminuria and a human FMO3 mutation database.

Hernandez D, Addou S, Lee D, Orengo C, Shephard EA, Phillips IR.

Hum Mutat. 2003 Sep;22(3):209-13. Review.

PMID:
12938085

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