Sulphur Amino Acids-Reference-Cited by-同舟云学术

Sulphur Amino Acids

Published:2013-01-28 Issue: Volume: Page:33-46
ISSN:
Container-title:Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases
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Author:

Barić Ivo,Fowler Brian

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/978-3-642-40337-8_3

Reference25 articles.

1. Augoustides-Savvopoulou P, Luka Z, Karyda S et al (2003) Glycine N-methyltransferase deficiency: A new patient with a novel mutation. J Inherit Metab Dis 26:745–759

2. Barić I, Fumić K, Glenn B et al (2004) S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism. Proc Nat Acad Sci U S A 101:4234–4239

3. Barić I, Ćuk M, Fumić K et al (2005) S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy. J Inherit Metab Dis 28:885–902

4. Bjursell MK, Blom HJ, Cayuela JA et al (2011) Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function. Am J Hum Genet 89:507–515

5. Braverman NE, Mudd SH, Barker PB, Pomper MG (2005) Characteristic MR imaging changes in severe hypermethioninemic states. AJNR Am J Neuroradiol 26:2705–2706

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