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Pediatric Clinical Chemistry
Citations 151-160 of 264 total displayed.
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Past content
(since Jan 1997):
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- Letters to the Editor
Monitoring Neonatal Hypoglycemia with the Accu-chek Advantage II Glucose Meter: The Cautionary Tale of Galactosemia
- Julie D. Newman, C. Andrew Ramsden, and Nicholas D.H. Balazs
Clin. Chem. 2002; 48: 2071.
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- Proteomics and Protein Markers
Neopterin and Quinolinic Acid Are Surrogate Measures of Disease Activity in the Juvenile Idiopathic Inflammatory Myopathies
- Lisa G. Rider, Adam S. Schiffenbauer, Mark Zito, Ken L. Lim, Alaa Ahmed, Lawrence S. Zemel, Robert M. Rennebohm, Murray H. Passo, Ronald M. Summers, Jeanne E. Hicks, Peter A. Lachenbruch, Melvyn P. Heyes, and Frederick W. Miller
Clin. Chem. 2002; 48: 1681-1688.
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- Pediatric Clinical Chemistry
Guanidinoacetate and Creatine plus Creatinine Assessment in Physiologic Fluids: An Effective Diagnostic Tool for the Biochemical Diagnosis of Arginine:Glycine Amidinotransferase and Guanidinoacetate Methyltransferase Deficiencies
- Claudia Carducci, Maurizio Birarelli, Vincenzo Leuzzi, Carla Carducci, Roberta Battini, Giovanni Cioni, and Italo Antonozzi
Clin. Chem. 2002; 48: 1772-1778.
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- Technical Briefs
Improved Matrix-assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometric Method for Identification of Amino Acid O-Glycosides in Patients with  -N-Acetylgalactosaminidase Deficiency
- Masahisa Horiuchi, Tomoko Fukushige, Takeyori Saheki, and Tamotsu Kanzaki
Clin. Chem. 2002; 48: 1798-1799.
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- Editorials
A Hematologic "Gold Standard" for Iron-deficient States?
- Carlo Brugnara
Clin. Chem. 2002; 48: 981-982.
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- Hematology
Biochemical Markers and Hematologic Indices in the Diagnosis of Functional Iron Deficiency
- Christian Thomas and Lothar Thomas
Clin. Chem. 2002; 48: 1066-1076.
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- Molecular Diagnostics and Genetics
Multiplex Minisequencing of the 21-Hydroxylase Gene as a Rapid Strategy to Confirm Congenital Adrenal Hyperplasia
- Nils Krone, Andreas Braun, Stefanie Weinert, Michael Peter, Adelbert A. Roscher, Carl-Joachim Partsch, and Wolfgang G. Sippell
Clin. Chem. 2002; 48: 818-825.
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- Molecular Diagnostics and Genetics
Analysis of Carnitine Biosynthesis Metabolites in Urine by HPLC–Electrospray Tandem Mass Spectrometry
- Frédéric M. Vaz, Bela Melegh, Judit Bene, Dean Cuebas, Douglas A. Gage, Albert Bootsma, Peter Vreken, Albert H. van Gennip, Loran L. Bieber, and Ronald J.A. Wanders
Clin. Chem. 2002; 48: 826-834.
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- Molecular Diagnostics and Genetics
5,10-Methylenetetrahydrofolate Reductase (MTHFR) Assay in the Forward Direction: Residual Activity in MTHFR Deficiency
- Terttu Suormala, Gertraud Gamse, and Brian Fowler
Clin. Chem. 2002; 48: 835-843.
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- Letters to the Editor
More on the Metabolic Autopsy
- Anne Green, Mary Anne Preece, and David Hardy
Clin. Chem. 2002; 48: 964-a-965-a.
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