Cerebrospinal fluid amino acids, purines and pyrimidines as a tool in the study of metabolic brain diseases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00711899
Reference20 articles.
1. Applegarth DA, Edelsten AD, Wong LTK, Morrison BJ (1979) Observed range of assay values for plasma and cerebrospinal fluid amino acid levels in infants and children aged 3 months to 10 years.Clin Biochem 12: 173?178.
2. Bakkeren JAJM, De Abreu RA, Sengers RCA, Gabreëls FJM, Maas JM, Renier WO (1984) Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dehydrothymine dehydrogenase deficiency.Clin Chim Acta 14: 247?256.
3. Cangiano C, Cardelli-Cangiano P, Cascino A, Ceci F, Fiori A, Mulieri M, Muscaritoli M, Barberini C, Strom R, Fanelli FR (1988) Uptake of amino acids by brain microvessels from rats with experimental chronic renal failure.J Neurochem 51: 1675?1681.
4. Ferraro TN, Hare TA (1985) Free and conjugated amino acids in human CSF: influence of age and sex.Brain Res 338: 53?60.
5. Gerrits GPJM, Haagen AAM, De Abreu RA, Monnens LAH, Gabreëls FJM, Trijbels JMF, Theeuwes ALM, Van Baal JM (1988) Reference values for nucleosides and nucleobases in cerebrospinal fluid of children.Clin Chem 34: 1439?1442.
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1. Neurometabolic Testing in Developmental Delay;Journal of Child Neurology;2000-09
2. Diagnosis of developmental delay: the metabolic biochemist's approach;Current Paediatrics;1994-12
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