1. John Caffey

   • H. -R. Wiedemann

   The Pioneers of Pediatric Medicine Pages: 141 - 141

2. Copper and liver disease

   • D. M. Danks

   Review Pages: 142 - 148

3. Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies

   • B. P. Hauffa
   • J. Sólyom
   • J. Homoki

   Endocrinology Pages: 149 - 153

4. Massive breast enlargement in an infant girl with central nervous system dysfunction

   • G. J. Mick
   • K. L. McCormick
   • H. Wakimoto

   Endocrinology Pages: 154 - 157

5. Intestinal ultrasonographic findings in Schönlein-Henoch syndrome

   • T. Bömelburg
   • U. Claasen
   • H. -J. von Lengerke

   Gastroenterology/Hepatology Pages: 158 - 160

6. Diagnosis of chronic granulomatous disease and of its mode of inheritance by dihydrorhodamine 123 and flow microcytofluorometry

   • J. Roesler
   • M. Hecht
   • A. Emmendörffer

   Hematology Pages: 161 - 165

7. Radionuclide bone imaging in toddler's fracture

   • K. De Boeck
   • S. Van Eldere
   • M. Casteels-Van Daele

   Imaging Techniques Pages: 166 - 169

8. Intra-articular steroids in pauciarticular juvenile chronic arthritis, type 1

   • R. Hertzberger-ten Cate
   • B. C. M. de Vries-van der Vlugt
   • A. Cats

   Immunology Pages: 170 - 172

9. Increased whole blood chemiluminescence in patients with Shwachman syndrome: therapy trial with thiamine and α-tocopherol

   • M. Ristola
   • E. Savilahti
   • H. Repo

   Immunology Pages: 173 - 178

10. The changes of interleukin-2, tumour necrotic factor and gamma-interferon production among patients with Kawasaki disease

    • C. -Y. Lin
    • C. -C. Lin
    • B. N. Chiang

    Infectious Diseases Pages: 179 - 182

11. Haemophilus influenzae epiglottitis occurring simultaneously in two siblings

    • M. Trop
    • G. Zobel
    • M. Mokry

    Infectious Diseases Pages: 183 - 184

12. Disturbed myelination in patients with treated hyperphenylalaninaemia: evaluation with magnetic resonance imaging

    • U. Bick
    • G. Fahrendorf
    • K. Ullrich

    Metabolic Diseases Pages: 185 - 189

13. 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

    • M. Duran
    • R. J. A. Wanders
    • F. J. van Sprang

    Metabolic Diseases Pages: 190 - 195

14. Infantile isolated sulphite oxidase deficiency: Report of a case with negative sulphite test and normal sulphate excretion

    • J. M. van der Klei-van Moorsel
    • L. M. E. Smit
    • M. Duran

    Metabolic Diseases Pages: 196 - 197

15. Mitochondrial phosphoenolpyruvate carboxykinase deficiency

    • J. V. Leonard
    • K. Hyland
    • P. T. Clayton

    Metabolic Diseases Pages: 198 - 199

16. Polygraphic sleep patterns and growth hormone secretion in children after cranial irradiation

    • I. Fagioli
    • R. Brauner
    • R. Rappaport

    Neuropediatrics Pages: 200 - 204

17. Maternal vegan diet causing a serious infantile neurological disorder due to vitamin B₁₂ deficiency

    • T. Kühne
    • R. Bubl
    • R. Baumgartner

    Nutrition Pages: 205 - 208

18. Influence of short- and long-term inhalation of salbutamol on lung function and β₂-andrenoceptors of mononuclear blood cells in asthmatic children

    • A. Schuster
    • R. Kozlik
    • D. Reinhardt

    Pneumology Pages: 209 - 213

19. Daycare attendance and risk of first infectious disease

    • J. P. Collet
    • T. Ducruet
    • J. -P. Boissel

    Pneumology Pages: 214 - 216

20. Massive overdose with thyroxine, —toxicity and treatment

    • G. K. Singh
    • M. H. Winterborn

    Letters to the Editors Pages: 217 - 217

21. Septic arthritis associated withHaemophilus influenzae meningitis

    • W. Courtens
    • H. De Boeck
    • J. Ramet

    Letters to the Editors Pages: 217 - 218

22. Announcement

    Announcement Pages: 218 - 218