1. The pioneers of pediatric medicine

   • H. -R. Wiedemann

   Announcement Pages: 531 - 531

2. The cephalosporin antibiotics in pediatric therapy

   • H. F. Eichenwald
   • H. J. Schmitt

   Review Pages: 532 - 538

3. Ventilatory response to CO₂ in infants with alleged sleep apnoea

   • H. Folgering
   • J. Boon

   Original Investigations Pages: 539 - 544

4. Partial exchange transfusion using peripheral vessels in polycythaemic newborn infants

   • A. Scarcella
   • P. Gambardella

   Original Investigations Pages: 545 - 546

5. Variations in dried blood spot immunoreactive trypsin in relation to gestational age and during the first week of life

   • J. P. Bourguignon
   • G. Deby-Dupont
   • P. Franchimont

   Original Investigations Pages: 547 - 549

6. Compensatory maturational deceleration of growth or “catch-down growth” in patients with congenital adrenal hyperplasia after delayed initiation of therapy

   • U. Hunziker
   • R. Largo
   • A. Prader

   Original Investigations Pages: 550 - 553

7. Captopril in severe childhood hypertension—Reversible anaemia with high dosage

   • H. A. Verhaaren
   • J. Vande Walle
   • A. Devloo-Blancquaert

   Original Investigations Pages: 554 - 556

8. Childhood neuromuscular disease with rimmed vacuoles

   • H. H. Goebel
   • S. von Loh
   • J. Gehler

   Original Investigations Pages: 557 - 562

9. Rett syndrome revisited: A patient with biotin dependency

   • C. Bachmann
   • J. Schaub
   • B. Wolf

   Original Investigations Pages: 563 - 566

10. Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect

    • E. A. Haan
    • R. D. Scholem
    • G. K. Brown

    Original Investigations Pages: 567 - 570

11. Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)

    • I. Lombeck
    • U. Wendel
    • S. Wadman

    Original Investigations Pages: 571 - 573

12. The Dubowitz syndrome

    • W. Küster
    • F. Majewski

    Original Investigations Pages: 574 - 578

13. LADD syndrome: report of new cases and review of the clinical spectrum

    • H. -R. Wiedemann
    • J. Drescher

    Original Investigations Pages: 579 - 582

14. Pachymeningitis presenting feature of posterior sinus infection

    • A. Leiberman
    • F. Tovi
    • M. Hirsch

    Original Investigations Pages: 583 - 585

15. 3-Ketothiolase deficiency

    • B. Middleton
    • K. Bartlett
    • W. L. Nyhan

    Short Communications Pages: 586 - 589

16. Dystonia as a presenting sign of subacute necrotising encephalomyelopathy in infancy

    • J. Campistol
    • V. Cusi
    • E. Fernandez-Alvarez

    Short Communications Pages: 589 - 591

17. Urinary microscopy in the diagnosis of haematuria in schönlein-henoch purpura

    • A. Martini
    • A. Ravelli
    • G. Beluffi

    Short Communications Pages: 591 - 593

18. Infantile multisystem inflammatory disease: another case of a new syndrome

    • F. Lampert

    Case Report Pages: 593 - 596

19. Bronchoscopic treatment of necrotising tracheo-bronchitis in a newborn

    • P. J. J. Sauer
    • E. J. v. d. Schans
    • H. N. Lafeber

    Letters to the Editors Pages: 596 - 597

20. Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material

    • E. A. Kvittingen
    • Pr. P. Guibaud
    • E. Christensen

    Letters to the Editors Pages: 597 - 598

21. Serum zinc concentrations in exclusively breast-fed infants and in infants fed an adapted formula

    • J. P. van Wouwe
    • C. J. A. van den Hamer
    • Vittorio Vigi

    Letters to the Editors Pages: 598 - 599

22. Announcement

    Announcement Pages: 600 - 600

23. 63rd Annual General Meeting of the Scottish Paediatric Society

    Abstracts Pages: 601 - 604