MEBO Research is a
EURORDIS and
NORD Member Organization
See RareConnect
Metabolomic Profiling Study

Start : Aug 2016
Stage 1 : 27 Canadian volunteers to test
Latest : Awaiting samples from participants above
Links :
clinicaltrials.gov
latest posts
Note : Stage 1 is Canada only

MEBO malodor map

Herbal Hill
Deodorising Products
see this post
Herbal Hill site
Facebook Page

TMAU Test through MEBO Research

MEBO Research International
TMAU Urine Test
Click here for
REQUISITION FORM
SEE UPDATES HERE
$150 plus
shipping costs

for one test,

$250plus
shipping costs

for 2 tests over time.
TWO PAYMENT PLAN OPTION
Send email to maria.delatorre@meboresearch.org to arrange, AFTER filling out Requisition Form, please.


Test analysis performed in batches of 20

DATE: 22 JUNE 2016
Now on : Program Resumed 5 July 2016
Samples analyzed since June 2012 : 287

Test analysis performed in batches of 20

Sonya's TMAU diet book

One of our group, Sonya McClinton, has written a 'low choline' recipe book. If you buy from Amazon through these links MEBO get a small % at no extra cost to the buyer


Amazon USA
38 sold

Amazon UK
14 sold
Don't have a kindle ? There are details on the right-side of the amazon pages how to download an app for smartphones, PC, or tablet. For Spain/Canada use the Amazon links in the left sidebar

tell others: send these links
Amazon USA : http://goo.gl/iisvYR
Amazon UK : http://goo.gl/mH2ZyN
BannerFans.com
RESEARCH DETAILS

DONATIONS THRU 31-MAY-2015:
£ 913.03/GBP
$ 568.00/USD

TOTAL at today's ROE
£0.6537/GBP = $1.00/USD

£1,281.23 = $1,948.81

MEBO UK PAYPAL FOR TRINZYME

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MEBO US PAYPAL FOR TRINZYME

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Blog Archive

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:
http://www.springerlink.com/content/542235781n315104/

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