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March20 podcast Dr Hazen
anti-TMA pill in a year or 2 ? (scroll 12 mins)

Additional info:
MEBO Karen
at UK Findacure conf 2020

Scroll down and select country

MEBO Map Testing & Meetups

Full details :
want listed ? contact

MEBO - UBIOME study 2018



MEBO Gut Microbiome Study
"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"
Funded by uBiome Research Grant

"Microbial Basis of Systemic Malodor and PATM Conditions (PATM)"

Dynamics of the Gut Microbiota in
Idiopathic Malodor Production

Started May 2018 - Ongoing

Current people sent kits : 100/100
3 kits per person


Participation info : LINK English

MEBO Private Facebook Group
to join : go to
or contact
Join/Watch the weekly
BO Sufferers Podcasts



TMAU Petition world
TMAU UK end total:262
TMAU UK ends 23/01/20
TMAU Petition USA end total 204
USA : Moveon open
TMAU (Dominican)
Metabolomic Profiling Study

Start : Aug 2016
Stage 1 : 27 Canadian volunteers to test
Latest click here (26 oct) :
17 samples returned

Note : Stage 1 is Canada only.
Return cut-off date : passed
Analysis can take 6/8 weeks
Analysis start in/before Nov
MEBO Research is a
NORD Member Organization
See RareConnect

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MEBO Research Clinical Trials

Friday, April 11, 2008

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children

Journal of Inherited Metabolic Disease Volume 29, Number 1 / February, 2006
R. A. Chalmers, M. D. Bain, H. Michelakakis, J. Zschocke and R. A. Iles (
1) Paediatric Metabolism Unit, St George’s Hospital Medical School, London, UK
(2) Institute of Child Health, Aghia Sophia Children’s Hospital, Athens, Greece
(3) Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany
(4) Department of Diabetes and Metabolic Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary College, London, UK
(5) Present address: CIMOA, London BioScience Innovation Centre, 2 Royal College Street, London, NW1 0NH, UK

Persistent trimethylaminuria in children is caused by autosomal recessively inherited impairment of hepatic trimethylamine (TMA) oxidation due to deficiency of flavin monooxygenase 3 (FMO3) secondary to mutations in the FMO3 gene...

full article:


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