(Q83120596)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

R A Chalmers

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

M D Bain

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

H Michelakakis

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

J Zschocke

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

R A Iles

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

1 February 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

162-172

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16601883%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10545-006-0158-6

19 January 2020

exact match

0 references

cites work

Trimethylaminuria and a human FMO3 mutation database

1 reference

12 December 2020

Choline and L-carnitine as precursors of trimethylamine

1 reference

12 December 2020

Trimethylaminuria: fishy odors in children

1 reference

12 December 2020

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

1 reference

12 December 2020

Fish odour syndrome with features of both primary and secondary trimethylaminuria.

1 reference

12 December 2020

Trimethylaminuria: diet does not always control the fishy odor

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy

1 reference

12 December 2020

Living with water stress: evolution of osmolyte systems

1 reference

12 December 2020

Dietary precursors of trimethylamine in man: a pilot study

1 reference

12 December 2020

Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication

1 reference

12 December 2020

Trimethylaminuria: the fish malodor syndrome

1 reference

12 December 2020

Trimethylamine oxide accumulation in marine animals: relationship to acylglycerol storage.

1 reference

12 December 2020

Trimethylamine N-oxide synthesis: a human variant

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort

1 reference

12 December 2020

Mild trimethylaminuria caused by common variants in FMO3 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Trimethylaminuria: the fish-odour syndrome

1 reference

12 December 2020