Literature DB >> 18928446

Trimethylaminuria (fish malodour syndrome): a "benign" genetic condition with major psychosocial sequelae.

Helen Mountain, Joanna M Brisbane, Amanda J Hooper, John R Burnett, Jack Goldblatt.   

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Year:  2008        PMID: 18928446     DOI: 10.5694/j.1326-5377.2008.tb02126.x

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


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  6 in total

1.  A pilot study of the effect of (e, e)-2, 4-undecadienal on the offensive odour of trimethylamine.

Authors:  Pankaj Garg; Kevin Carpenter; Shanley Chong; John Christodoulou
Journal:  JIMD Rep       Date:  2012-05-23

2.  Trimethylaminuria: causes and diagnosis of a socially distressing condition.

Authors:  Richard J Mackay; Christopher J McEntyre; Caroline Henderson; Michael Lever; Peter M George
Journal:  Clin Biochem Rev       Date:  2011-02

Review 3.  A review of trimethylaminuria: (fish odor syndrome).

Authors:  Jeffrey Messenger; Shane Clark; Susan Massick; Mark Bechtel
Journal:  J Clin Aesthet Dermatol       Date:  2013-11

4.  A compound heterozygous mutation in the FMO3 gene: the first pediatric case causes fish odor syndrome in Korea.

Authors:  Ji Hyun Kim; Sung Min Cho; Jong-Hee Chae
Journal:  Korean J Pediatr       Date:  2017-03-27

5.  Endovascular Closure Resolves Trimethylaminuria Caused by Congenital Portosystemic Shunts.

Authors:  María Dolores Ponce-Dorrego; Gonzalo Garzón-Moll
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2019-11-07

6.  Impact of trimethylaminuria on daily psychosocial functioning.

Authors:  Daniel Roddy; Philomena McCarthy; Darragh Nerney; Jennifer Mulligan-Rabbitt; Edwin Smith; Eileen P Treacy
Journal:  JIMD Rep       Date:  2020-10-06
  6 in total

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