Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap

Author:

Harvey Mudd S,Braverman Nancy,Pomper Martin,Tezcan Kamer,Kronick Jonathan,Jayakar Parul,Garganta Cheryl,Ampola Mary G,Levy Harvey L,McCandless Shawn E,Wiltse Hobart,Stabler Sally P,Allen Robert H,Wagner Conrad,Borschel Marlene W

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference30 articles.

1. Energy;Fomon,1993

2. Screening for “inborn errors of metabolism” in the newborn infant—a multiple test program;Guthrie;Birth Defects,1968

3. Rapid diagnosis of homocystinuria and other hypermethioninemias from newborns’ blood spots by tandem mass spectrometry;Chace;Clin. Chem.,1996

4. Metabolic abnormalities in cobalamin (vitamin B12) and folate deficiency;Allen;FASEB J.,1993

5. Elevation of serum cystathionine levels in patients with cobalamin and folate deficiency;Stabler;Blood,1993

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