Newborn screening by tandem mass spectrometry gaining experience

Clinical Chemistry

Volumn 47, Issue 11, 2001, Pages 1937-1938

  Sweetman, L ^a  

^a BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD ANALYSIS; BLOOD STAIN; EDITORIAL; LABORATORY DIAGNOSIS; METABOLIC DISORDER; NEWBORN SCREENING; TANDEM MASS SPECTROMETRY;

EID: 0034780874     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/47.11.1937     Document Type: Editorial

References (18)

1. Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism
2. The analysis of diagnostic markers of genetic disorders to human blood and urine using tandem mass spectrometry with liquid secondary ion mass spectrometry
3. Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry
4. Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 h
5. Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry
6. Rapid diagnosis of homocystinuria and other hypermethioninemias from newborns' blood spots by tandem mass spectrometry
7. Rapid diagnosis of MCAD deficiency: Quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry
8. Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid β-oxidation
9. Rapid screening of high-risk patients for disorders of purine and pyrimidine metabolism using HPLC-electrospray tandem mass spectrometry of liquid urine or urine-soaked filter paper strips
10. Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometry
11. The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots
12. Screening blood spots for inborn errors of metabolism by electrospray tandem mass spectrometry with a microplate batch process and a computer algorithm for automated flagging of abnormal profiles
13. Newborn screening with tandem mass spectrometry 12 months' experience in NSW Australia
14. Newborn screening by tandem mass spectrometry (MS-MS)
15. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: A two-year summary from the New England Newborn Screening Program
16. Newborn screening by tandem mass spectrometry: A new era
17. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mile MCAD deficiency