Betaine dose and treatment intervals in therapy for homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency-Reference-Cited by-同舟云学术

Betaine dose and treatment intervals in therapy for homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency

Published:1998-02 Issue:1 Volume:21 Page:84-85
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Sakura N.,Ono H.,Nomura S.,Ueda H.,Fujita N.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005331902497/fullpdf

Reference4 articles.

1. Serum betaine, N, N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism;Allen;Metabolism,1993

2. Effect of betaine on S-adenosylmethionine levels in the cerebrospinal fluid in a patient with methylenetetrahydrofolate reductase deficiency and 55 peripheral neuropathy;Kishi;J Inher Metab Dis,1994

3. High performance liquid chromatographic determination of human serum betaine and its clinical trial in the betaine treatment of homocystinuria;Sakura;J Jpn P ediatr Soc,1997

4. Human hepatic methionine 60 biosynthesis;Skiba;J Biol Chem,1982

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