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Select item 78026211.

Impact of trimethylaminuria on daily psychosocial functioning

Daniel Roddy, Philomena McCarthy, Darragh Nerney, Jennifer Mulligan‐Rabbitt, Edwin Smith, Eileen P. Treacy

JIMD Rep. 2021 Jan; 57(1): 67–75. Published online 2020 Oct 6. doi: 10.1002/jmd2.12170

PMCID:: PMC7802621

Abstract Article PDF–1.0M

Select item 68565092.

Endovascular Closure Resolves Trimethylaminuria Caused by Congenital Portosystemic Shunts

María Dolores Ponce-Dorrego, Gonzalo Garzón-Moll

Pediatr Gastroenterol Hepatol Nutr. 2019 Nov; 22(6): 588–593. Published online 2019 Nov 7. doi: 10.5223/pghn.2019.22.6.588

PMCID:: PMC6856509

Abstract Article PDF–893K

Select item 67518753.

Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: ¹H NMR spectroscopy and genetic testing

Nadia Bouchemal, Lisa Ouss, Anaïs Brassier, Valérie Barbier, Stéphanie Gobin, Laurence Hubert, Pascale de Lonlay, Laurence Le Moyec

Orphanet J Rare Dis. 2019; 14: 222. Published online 2019 Sep 18. doi: 10.1186/s13023-019-1174-6

PMCID:: PMC6751875

Abstract Article PDF–469K

Select item 64988254.

The genetic and biochemical basis of trimethylaminuria in an Irish cohort

Samantha Doyle, James J. O'Byrne, Mandy Nesbitt, Daniel N. Murphy, Zaza Abidin, Niall Byrne, Gregory Pastores, Richard Kirk, Eileen P. Treacy

JIMD Rep. 2019 May; 47(1): 35–40. Published online 2019 Mar 25. doi: 10.1002/jmd2.12028

PMCID:: PMC6498825

Abstract Article PDF–680K

Select item 54713995.

Analysis of six novel flavin-containing monooxygenase 3 (FMO3) gene variants found in a Japanese population suffering from trimethylaminuria

Makiko Shimizu, Yumi Origuchi, Marika Ikuma, Nanako Mitsuhashi, Hiroshi Yamazaki

Mol Genet Metab Rep. 2015 Dec; 5: 89–93. Published online 2015 Nov 7. doi: 10.1016/j.ymgmr.2015.10.013

PMCID:: PMC5471399

Abstract Article PDF–682K

Select item 48541396.

Trimethylaminuria

Numaera Sabir, Elizabeth A Jones, Beena Padmakumar

BMJ Case Rep. 2016; 2016: bcr2015213742. Published online 2016 Apr 26. doi: 10.1136/bcr-2015-213742

PMCID:: PMC4854139

Abstract Article PDF–238K

Select item 41905927.

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report

Rosalia D’Angelo, Concetta Scimone, Teresa Esposito, Daniele Bruschetta, Carmela Rinaldi, Alessia Ruggeri, Antonina Sidoti

J Med Case Rep. 2014; 8: 328. Published online 2014 Oct 6. doi: 10.1186/1752-1947-8-328

PMCID:: PMC4190592

Abstract Article PDF–254K

Select item 40499378.

Archaebiotics: Proposed therapeutic use of archaea to prevent trimethylaminuria and cardiovascular disease

Jean-François Brugère, Guillaume Borrel, Nadia Gaci, William Tottey, Paul W O’Toole, Corinne Malpuech-Brugère

Gut Microbes. 2014 Jan 1; 5(1): 5–10. Published online 2013 Oct 31. doi: 10.4161/gmic.26749

PMCID:: PMC4049937

Abstract Article PDF–1.9M

Select item 40044049.

Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population

Makiko Shimizu, Charles K Allerston, Elizabeth A Shephard, Hiroshi Yamazaki, Ian R Phillips

Br J Clin Pharmacol. 2014 May; 77(5): 839–851. Published online 2014 Apr 22. doi: 10.1111/bcp.12240

PMCID:: PMC4004404

Abstract Article PDF–1.1M

Select item 389778810.

Transient Massive Trimethylaminuria Associated with Food Protein–Induced Enterocolitis Syndrome

Natalie B. Miller, Avraham Beigelman, Elizabeth Utterson, Marwan Shinawi

JIMD Rep. 2014; 12: 11–15. Published online 2013 Jul 3. doi: 10.1007/8904_2013_238

PMCID:: PMC3897788

Abstract Article PDF–125K

Select item 384865211.

A Review of Trimethylaminuria: (Fish Odor Syndrome)

Jeffrey Messenger, Shane Clark, Susan Massick, Mark Bechtel

J Clin Aesthet Dermatol. 2013 Nov; 6(11): 45–48.

PMCID:: PMC3848652

Abstract Article PDF–9.9M

Select item 373840212.

Trimethylaminuria (fish malodour syndrome) in chronic renal failure

E Hur, O Gungor, D Bozkurt, SMK Bozgul, F Dusunur, H Caliskan, A Berdeli, F Akcicek, A Basci, S Duman

Hippokratia. 2012 Jan-Mar; 16(1): 83–85.

PMCID:: PMC3738402

Abstract Article PDF–480K

Select item 350992513.

Riboflavin-Responsive Trimethylaminuria in a Patient with Homocystinuria on Betaine Therapy

Nigel J. Manning, Elizabeth K. Allen, Richard J. Kirk, Mark J. Sharrard, Edwin J. Smith

JIMD Rep. 2012; 5: 71–75. Published online 2011 Nov 20. doi: 10.1007/8904_2011_99

PMCID:: PMC3509925

Abstract Article PDF–92K

Select item 305239214.

Trimethylaminuria: Causes and Diagnosis of a Socially Distressing Condition

Richard J Mackay, Christopher J McEntyre, Caroline Henderson, Michael Lever, Peter M George

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

PMCID:: PMC3052392

Abstract Article PDF–408K

Select item 273959315.

Novel Variants of the Human Flavin-Containing Monooxygenase 3 (FMO3) Gene Associated with Trimethylaminuria

Meike S. Motika, Jun Zhang, Xueying Zheng, Kiersten Riedler, John R. Cashman

Mol Genet Metab. Author manuscript; available in PMC 2010 Jun 1.

Published in final edited form as: Mol Genet Metab. 2009 Jun; 97(2): 128–135. Published online 2009 Feb 27. doi: 10.1016/j.ymgme.2009.02.006

PMCID:: PMC2739593

Abstract Article PDF–321K

Select item 203992116.

Functional Characterization of Genetic Variants of Human FMO3 Associated with Trimethylaminuria

Catherine K. Yeung, Elinor T. Adman, Allan E. Rettie

Arch Biochem Biophys. Author manuscript; available in PMC 2008 Aug 15.

Published in final edited form as: Arch Biochem Biophys. 2007 Aug 15; 464(2): 251–259. Published online 2007 May 2. doi: 10.1016/j.abb.2007.04.014

PMCID:: PMC2039921

Abstract Article PDF–927K

Select item 179088517.

Transient trimethylaminuria related to menstruation

Makiko Shimizu, John R Cashman, Hiroshi Yamazaki

BMC Med Genet. 2007; 8: 2. Published online 2007 Jan 27. doi: 10.1186/1471-2350-8-2

PMCID:: PMC1790885

Abstract Article PDF–267K

Select item 966767518.

FMO3 deficiency of duck leads to decreased lipid deposition and increased antibacterial activity

Xingzheng Li, Jianlou Song, Xuefeng Shi, Mingyi Huang, Lei Liu, Guoqiang Yi, Ning Yang, Guiyun Xu, Jiangxia Zheng

J Anim Sci Biotechnol. 2022; 13: 119. Published online 2022 Nov 16. doi: 10.1186/s40104-022-00777-1

PMCID:: PMC9667675

Abstract Article PDF–4.4M

Select item 861876819.

Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Simona Alibrandi, Fabiana Nicita, Luigi Donato, Concetta Scimone, Carmela Rinaldi, Rosalia D’Angelo, Antonina Sidoti

Molecules. 2021 Nov; 26(22): 7045. Published online 2021 Nov 22. doi: 10.3390/molecules26227045

PMCID:: PMC8618768

Abstract Article PDF–3.6M

Select item 791209820.

Gut-Brain Axis Cross-Talk and Limbic Disorders as Biological Basis of Secondary TMAU

Luigi Donato, Simona Alibrandi, Concetta Scimone, Andrea Castagnetti, Giacomo Rao, Antonina Sidoti, Rosalia D’Angelo

J Pers Med. 2021 Feb; 11(2): 87. Published online 2021 Jan 31. doi: 10.3390/jpm11020087

PMCID:: PMC7912098

Abstract Article PDF–3.5M

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