Diagnosis of maple syrup urine disease by determination of L-valine, L-isoleucine, L-leucine and L-phenylalanine in neonatal blood spots by gas chromatography-mass spectrometry

Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

Volumn 792, Issue 2, 2003, Pages 261-268

  Deng, Chunhui ^a   Deng, Yonghui ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

Isoleucine; Leucine; Maple syrup urine disease; Phenylalanine; Valine

Indexed keywords

AMINO ACIDS; DERIVATIVES; DIAGNOSIS; EXTRACTION; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY;

BLOOD SPOTS;

BODY FLUIDS;

AMINO ACID DERIVATIVE; BUTANOL; ISOLEUCINE; LEUCINE; METHANOL; PHENYLALANINE; TRIFLUOROACETIC ACID; VALINE;

AMINO ACID ANALYSIS; ARTICLE; BLOOD ANALYSIS; DIAGNOSTIC PROCEDURE; EXTRACTION; GAS CHROMATOGRAPHY; HUMAN; ION MONITORING; MAPLE SYRUP URINE DISEASE; MASS SPECTROMETRY; NEWBORN; NEWBORN PERIOD; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS;

ACER;

EID: 0038306717     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1570-0232(03)00270-8     Document Type: Article

References (26)

1. Matsumoto I., Sakamoto S., Kuhara T., Sudo M., Yoshino M. GC-MS Practical Chemical Diagnosis - Inherited Metabolic Disorders. 1995;Soft Science Publications, Tokyo.
2. Deyl Z., Hyanek J., Horakova M. J. Chromatogr. 379:1986;177.
3. Kuhara T., Matsumoto I. Proc. Jpn. Soc. Biomed. Mass Spectrom. 20:1995;45.
4. Kuhara T. J. Chromatogr. B. 758:2001;3.
5. Rashed M.S. J. Chromatogr. B. 758:2001;27.
6. Bruckner H., Schieber A. Biomed. Chromatogr. 15:2001;166.
7. Kuhara T., Shinka T., Inoue Y., Ohse M., Zhen-Wei X., Yashida I., Inokuchi T., Yamaguchi S., Takayanagi M., Matsumoto I. J. Chromatogr. B. 731:1999;141.
8. Marquez C.D., Weintraub S.T., Smith P.C. J. Chromatogr. B. 658:1994;213.
9. Stabler S.P., Marcell P.D., Podell E.R., Allen R.H. Anal. Chem. 162:1987;185.
10. Zhang C., Matsumoto M., Inoue Y., et al. J. Kanazawa Med. Univ. 21:1996;399.
11. Utsumomiya M., Nozaki T., Zhang C., et al. Proc. J. Jpn. Soc. Biomed. Mass Spectrom. 22:1997;119.
12. Molnar-Perl I., Katona Zs.F. Chromatographia. (Suppl. 51):2000;S228.
13. Jellum E., Horn L., Thoresen O. Scand. J. Clin. Lab. Invest. 184:1986;21.
14. Kaiser F.E., Gehrke C.W., Zumalt R.W. J. Chromatogr. 94:1974;113.
15. Zomezely C., Marco G., Emery E. Anal. Chem. 34:1962;1414.
16. Deng C.H., Shang C.Q., Hu Y.M. J. Chromatogr. B. 755:2002;115.
17. Deng C.H., Deng Y.H., Wang B. J. Chromatogr. B. 780:2002;245.
18. Scriver A.L., Beaudet W.S., Sly D.V. The Metabolic and Molecular Bases of Inherited Disease. 1995;McGraw-Hill, New York.
19. Tavares R.G., Santos C.E.S., Tasca A.I., Wajner M., Souza D.O., Dutra-Filho C.S. J. Neurol. Sci. 181:2000;44.
20. Pessoa-Pureur R., Funchal C., Pelaez P.D., Vivian L., Loureiro S.O., Miranda R.D., Wajner M. Metab. Brain Dis. 17:2002;65.
21. Efron M.L. New Engl. J. Med. 272:1965;1058.
22. Snyderman S.E., Norton P.M., Roitman E. Pediatrics. 34:1964;454.
23. Chace D.H., Hillman S.L., Millngton D.S., Kahler S.G. Clin. Chem. 41:1995;62.
24. Podebrad F., Heil M., Leib S., Geier B., Beck T. HRC-J. High Resolut. Chromatogr. 20:1997;355.
25. Qu Y., Slocum R.H., Fu J., Rasmussen W.E., Rector H.D., Miller J.B., Coldwell J.G. Clin. Chim. Acta. 312:2001;153.
26. Qu Y., Miller J.B., Slocum R.H. Clin. Chim. Acta. 203:1991;191.