1. Preface

   • G. F. Hoffmann
   • H. J. Bremer

   EditorialNotes Pages: S1 - S1

2. Selective screening for inborn errors of metabolism — past, present and future

   • G. F. Hoffmann

   OriginalPaper Pages: S2 - S8

3. Long-term results of selective screening for inborn errors of metabolism

   • Willy Lehnert

   OriginalPaper Pages: S9 - S13

4. Results of selective screening for inborn errors of metabolism in the former East Germany

   • G. Machill
   • U. Grimm
   • T. Schneider

   OriginalPaper Pages: S14 - S16

5. Quality control for selective screening of inborn errors of metabolism

   • F. A. Hommes

   OriginalPaper Pages: S17 - S22

6. Pitfalls in aminoacid and organic acid analysis: 3-Hydroxypropionic aciduria

   • C. Bachmann
   • O. Boulat
   • P. Pilloud

   OriginalPaper Pages: S23 - S26

7. Group tests for selective screening of inborn errors of metabolism

   • M. Duran
   • L. Dorland
   • R. Berger

   OriginalPaper Pages: S27 - S32

8. Selective screening for amino acid disorders

   • M. Duran
   • L. Dorland
   • R. Berger

   OriginalPaper Pages: S33 - S37

9. Screening for lysosomal disorders

   • K. Ullrich

   OriginalPaper Pages: S38 - S43

10. Clinical and biochemical characteristics of peroxisomal disorders: an update

    • R. J. A. Wanders
    • P. G. Barth
    • J. M. Tager

    OriginalPaper Pages: S44 - S48

11. New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation disorders

    • Paul M. Coates

    OriginalPaper Pages: S49 - S56

12. Carnitine esters in metabolic disease

    • H. Böhles
    • A. Evangeliou
    • A. Sewell

    OriginalPaper Pages: S57 - S61

13. Screening for defects of branched-chain amino acid metabolism

    • K. Michael Gibson
    • Carol F. Lee
    • Georg F. Hoffmann

    OriginalPaper Pages: S62 - S67

14. Propionic acidaemia: clinical, biochemical and therapeutic aspects

    • W. Lehnert
    • W. Sperl
    • E. R. Baumgartner

    OriginalPaper Pages: S68 - S80

15. The investigation of inborn errors in vivo using stable isotopes

    • J. V. Leonard
    • S. J. R. Heales

    OriginalPaper Pages: S81 - S83

16. DNA techniques for screening of inborn errors of metabolism

    • E. R. B. McCabe

    OriginalPaper Pages: S84 - S85

17. Cerebrospinal fluid as a tool in the diagnosis of neurometabolic diseases: amino acid analysis before and after acid hydrolysis

    • J. Jaeken

    OriginalPaper Pages: S86 - S89

18. Neuroradiological and neurophysiological indices for neurometabolic disorders

    • Alfried Kohlschütter

    OriginalPaper Pages: S90 - S93

19. Neurological manifestations of organic acid disorders

    • G. F. Hoffmann
    • K. M. Gibson
    • D. Rating

    OriginalPaper Pages: S94 - S100