227 related articles for article (PubMed ID: 1777980)
1. Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens.
Qu Y; Miller JB; Slocum RH; Shapira E
Clin Chim Acta; 1991 Dec; 203(2-3):191-7. PubMed ID: 1777980
[TBL] [Abstract][Full Text] [Related]
2. Neonatal screening for inborn errors of amino acid metabolism.
Levy HL
Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646
[No Abstract] [Full Text] [Related]
3. Development of micellar electro kinetic chromatography for the separation and quantitation of L-valine, L-leucine, L-isoleucin and L-phenylalanine in human plasma and comparison with HPLC.
Darvish M; Ebrahimi SA; Ghadam P
Pak J Biol Sci; 2007 Aug; 10(15):2436-41. PubMed ID: 19070110
[TBL] [Abstract][Full Text] [Related]
4. Isocratic reverse-phase liquid chromatography assay for amino acid metabolic disorders using eluates of dried blood spots.
Vollmer DW; Jinks DC; Guthrie R
Anal Biochem; 1990 Aug; 189(1):115-21. PubMed ID: 2278380
[TBL] [Abstract][Full Text] [Related]
5. 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.
Deng C; Deng Y
J Chromatogr B Analyt Technol Biomed Life Sci; 2003 Jul; 792(2):261-8. PubMed ID: 12860033
[TBL] [Abstract][Full Text] [Related]
6. [Experiences with a new amino acid analyzer for a rapid analysis].
Irtel von Brenndorff A; Hagge W
Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):417-9. PubMed ID: 5523694
[No Abstract] [Full Text] [Related]
7. Determination of branched chain amino acids, methionine, phenylalanine, tyrosine and alpha-keto acids in plasma and dried blood samples using HPLC with fluorescence detection.
Kand'ár R; Záková P; Jirosová J; Sladká M
Clin Chem Lab Med; 2009; 47(5):565-72. PubMed ID: 19290779
[TBL] [Abstract][Full Text] [Related]
8. A rapid procedure for the determination of phenylalanine and tyrosine from blood filter paper specimens.
Levy HL; Baullinger PC; Madigan PM
Clin Chim Acta; 1971 Feb; 31(2):447-52. PubMed ID: 5573686
[No Abstract] [Full Text] [Related]
9. Chromatographic diagnosis of maple syrup urine disease by measuring the L-alloisoleucine/L-phenylalanine ratio in dried blood spots.
Jeong JS; Sim HJ; Lee YM; Yoon HR; Kwon HJ; Hong SP
J Chromatogr B Analyt Technol Biomed Life Sci; 2011 Jul; 879(22):2171-4. PubMed ID: 21680261
[TBL] [Abstract][Full Text] [Related]
10. [A screening test for phenylketonuria using a paper chromatography method].
Halvorsen S; Skjelkvåle L
Lakartidningen; 1974 Mar; 71(12):1166-7. PubMed ID: 4821497
[No Abstract] [Full Text] [Related]
11. Multivariate discrimination for phenylketonuria (PKU) and non-PKU hyperphenylalaninemia after analysis of newborns' dried blood-spot specimens for six amino acids by ion-exchange chromatography.
Reilly AA; Bellisario R; Pass KA
Clin Chem; 1998 Feb; 44(2):317-26. PubMed ID: 9474031
[TBL] [Abstract][Full Text] [Related]
12. Semiquantitation of leucine, isoleucine, and valine by thin-layer chromatography in management of maple-syrup urine diseases.
Allen RJ; Frey HJ; Fleming LM; Owings CL
Clin Chem; 1972 May; 18(5):413-6. PubMed ID: 5019114
[No Abstract] [Full Text] [Related]
13. Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry.
Chace DH; Hillman SL; Millington DS; Kahler SG; Roe CR; Naylor EW
Clin Chem; 1995 Jan; 41(1):62-8. PubMed ID: 7813082
[TBL] [Abstract][Full Text] [Related]
14. Newborn screening may fail to identify intermediate forms of maple syrup urine disease.
Bhattacharya K; Khalili V; Wiley V; Carpenter K; Wilcken B
J Inherit Metab Dis; 2006 Aug; 29(4):586. PubMed ID: 16830261
[TBL] [Abstract][Full Text] [Related]
15. Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer.
Allard P; Cowell LD; Zytkovicz TH; Korson MS; Ampola MG
Clin Biochem; 2004 Oct; 37(10):857-62. PubMed ID: 15369715
[TBL] [Abstract][Full Text] [Related]
16. Neonatal screening in Italy for congenital hypothyroidism and metabolic disorders: hyperphenylalaninemia, maple syrup urine disease and homocystinuria.
Antonozzi I; Dominici R; Andreoli M; Monaco F
J Endocrinol Invest; 1980; 3(4):357-63. PubMed ID: 7204885
[TBL] [Abstract][Full Text] [Related]
17. Direct analysis of dried blood spots by in-line desorption combined with high-resolution chromatography and mass spectrometry for quantification of maple syrup urine disease biomarkers leucine and isoleucine.
Miller JH; Poston PA; Karnes HT
Anal Bioanal Chem; 2011 Apr; 400(1):237-44. PubMed ID: 21331490
[TBL] [Abstract][Full Text] [Related]
18. [Maple syrup urine disease and cystathioninemia].
Simma B; Sperl W; Berger H
Padiatr Padol; 1989; 24(1):69-75. PubMed ID: 2497426
[TBL] [Abstract][Full Text] [Related]
19. Recent advances in the early detection and treatment of inborn errors with brain damage.
Bickel H
Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066
[No Abstract] [Full Text] [Related]
20. HPLC for confirmatory diagnosis and biochemical monitoring of Cuban patients with hyperphenylalaninemias.
Contreras J; Alonso E; Fuentes LE
MEDICC Rev; 2015 Jan; 17(1):23-8. PubMed ID: 25725765
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]