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- BAUDHUIN P., HERS H. G., LOEB H. AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS. Lab Invest. 1964 Sep;13:1139–1152. [PubMed] [Google Scholar]
- Berry H. K., Leonard C., Peters H., Granger M., Chunekamrai N. Detection of metabolic disorders. Chromatographic procedures and interpretation of results. Clin Chem. 1968 Nov;14(11):1033–1065. [PubMed] [Google Scholar]
- Beutler E., Baluda M. C. A simple spot screening test for galactosemia. J Lab Clin Med. 1966 Jul;68(1):137–141. [PubMed] [Google Scholar]
- Buist N. R. Set of simple side-room urine tests for detection of inborn errors of metabolism. Br Med J. 1968 Jun 22;2(5607):745–749. doi: 10.1136/bmj.2.5607.745. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang T. M., Johnson L. J., Ransome O. J. Semipermeable aqueous microcapsules. IV. Nonthrombogenic microcapsules with heparin-complexed membranes. Can J Physiol Pharmacol. 1967 Jul;45(4):705–715. doi: 10.1139/y67-083. [DOI] [PubMed] [Google Scholar]
- Chang T. M., Poznansky M. J. Semipermeable microcapsules containing catalase for enzyme replacement in acatalasaemic mice. Nature. 1968 Apr 20;218(5138):243–245. doi: 10.1038/218243a0. [DOI] [PubMed] [Google Scholar]
- Clayton B. E., Francis D. E., Smith I. Synthetic diets in renal failure. Lancet. 1971 Aug 14;2(7720):380–381. doi: 10.1016/s0140-6736(71)90099-7. [DOI] [PubMed] [Google Scholar]
- Cusworth D. C., Dent C. E. Homocystinuria. Br Med Bull. 1969 Jan;25(1):42–47. doi: 10.1093/oxfordjournals.bmb.a070668. [DOI] [PubMed] [Google Scholar]
- Danes B. S., Bearn A. G. Cellular metachromasia, a genetic marker for studying the mucopolysaccharidoses. Lancet. 1967 Feb 4;1(7484):241–243. doi: 10.1016/s0140-6736(67)91302-5. [DOI] [PubMed] [Google Scholar]
- Danes B. S., Scott J. E., Bearn A. G. Further studies on metachromasia in cultured human fibroblasts. Staining of glycosaminoglycans (mucopolysaccharides) by Alcian blue in salt solutions. J Exp Med. 1970 Oct 1;132(4):765–774. doi: 10.1084/jem.132.4.765. [DOI] [PMC free article] [PubMed] [Google Scholar]
- EFRON M. L., YOUNG D., MOSER H. W., MACCREADY R. A. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER. N Engl J Med. 1964 Jun 25;270:1378–1383. doi: 10.1056/NEJM196406252702602. [DOI] [PubMed] [Google Scholar]
- GUTHRIE R., SUSI A. A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS. Pediatrics. 1963 Sep;32:338–343. [PubMed] [Google Scholar]
- Groth C. G., Hagenfeldt L., Dreborg S., Löfström B., Ockerman P. A., Samuelsson K., Svennerholm L., Werner B., Westberg G. Splenic transplantation in a case of Gaucher's disease. Lancet. 1971 Jun 19;1(7712):1260–1264. doi: 10.1016/s0140-6736(71)91778-8. [DOI] [PubMed] [Google Scholar]
- Hochella N. J., Hill J. B. Fluorometric screening procedure for galactosemia utilizing the autoanalyzer. Clin Chem. 1969 Oct;15(10):949–960. [PubMed] [Google Scholar]
- Hug G., Schubert W. K., Soukup S. Prenatal diagnosis of type-II glycogenosis. Lancet. 1970 May 9;1(7654):1002–1002. doi: 10.1016/s0140-6736(70)91128-1. [DOI] [PubMed] [Google Scholar]
- Jeffcoate T. N., Fliegner J. R., Russell S. H., Davis J. C., Wade A. P. Diagnosis of the adrenogenital syndrome before birth. Lancet. 1965 Sep 18;2(7412):553–555. doi: 10.1016/s0140-6736(65)90864-0. [DOI] [PubMed] [Google Scholar]
- Jellum E., Stokke O., Eldjarn L. Screening for metabolic disorders using gas-liquid chromatography, mass spectrometry, and computer technique. Scand J Clin Lab Invest. 1971 May;27(3):273–285. doi: 10.3109/00365517109080219. [DOI] [PubMed] [Google Scholar]
- Kissel P., Lamarche M., Royer R. Modification of uricaemia and the excretion of uric acid nitrogen by an enzyme of fungal origin. Nature. 1968 Jan 6;217(5123):72–74. doi: 10.1038/217072a0. [DOI] [PubMed] [Google Scholar]
- Komrower G. M., Griffiths M. J., Fowler B., Lambert A. M. A prospective community survey for aminoacidaemias. Proc R Soc Med. 1968 Mar;61(3):294–296. [PMC free article] [PubMed] [Google Scholar]
- MANN T. P., WILSON K. M., CLAYTON B. E. A DEFICIENCY STATE ARISING IN INFANTS ON SYNTHETIC FOODS. Arch Dis Child. 1965 Aug;40:364–375. doi: 10.1136/adc.40.212.364. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marchioro T. L., Hougie C., Ragde H., Epstein R. B., Thomas E. D. Hemophilia: role of organ homografts. Science. 1969 Jan 10;163(3863):188–190. doi: 10.1126/science.163.3863.188. [DOI] [PubMed] [Google Scholar]
- Milne M. D. Lessons from inborn errors of metabolism. Proc R Soc Med. 1966 Nov;59(11 Pt 1):1157–1162. [PMC free article] [PubMed] [Google Scholar]
- New M. I. Antenatal diagnosis of the adrenogenital syndrome. Lancet. 1970 Jan 10;1(7637):83–83. doi: 10.1016/s0140-6736(70)91868-4. [DOI] [PubMed] [Google Scholar]
- Nichols J. Antenatal diagnosis and treatment of the adrenogenital syndrome. Lancet. 1970 Jan 10;1(7637):83–83. doi: 10.1016/s0140-6736(70)91867-2. [DOI] [PubMed] [Google Scholar]
- Perry T. L., Hansen S., MacDougall L. Urinary screening tests in the prevention of mental deficiency. Can Med Assoc J. 1966 Jul 16;95(3):89–95. [PMC free article] [PubMed] [Google Scholar]
- SCRIVER C. R., DAVIES E., CULLEN A. M. APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES. Lancet. 1964 Aug 1;2(7353):230–232. doi: 10.1016/s0140-6736(64)90183-7. [DOI] [PubMed] [Google Scholar]
- Sutcliffe R. G., Brock D. J. Enzymes in uncultured amniotic fluid cells. Clin Chim Acta. 1971 Feb;31(2):363–365. doi: 10.1016/0009-8981(71)90404-9. [DOI] [PubMed] [Google Scholar]
- Taysi K., Kistenmacher M. L., Punnett H. H., Mellman W. J. Limitations of metachromasia as a diagnostic aid in pediatrics. N Engl J Med. 1969 Nov 13;281(20):1108–1111. doi: 10.1056/NEJM196911132812009. [DOI] [PubMed] [Google Scholar]
- WESTALL R. G. DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA). Arch Dis Child. 1963 Oct;38:485–491. doi: 10.1136/adc.38.201.485. [DOI] [PMC free article] [PubMed] [Google Scholar]