1. Samuel Zachary Levine

   • H. -R. Wiedemann

   Announcement Pages: 303 - 303

2. Spontaneous pneumomediastinum in children

   • F. G. A. Versteegh
   • I. A. J. M. Broeders

   Review Pages: 304 - 307

3. Persistent hyperthyrotropinaemia since the neonatal period in clinically euthyroid children

   • L. A. Tyfield
   • S. S. A. Abusrewil
   • D. C. L. Savage

   Endocrinology Pages: 308 - 309

4. Abnormal results of biochemical liver function tests in breast-fed infants with prolonged indirect hyperbilirubinaemia

   • Y. Tazawa
   • D. Abukawa
   • M. Yamada

   Gastroenterology/Hepatology Pages: 310 - 313

5. Coombs-positive giant cell hepatitis of infancy: effect of steroids and azathioprine therapy

   • B. Brichard
   • E. Sokal
   • G. Cornu

   Gastroenterology/Hepatology Pages: 314 - 317

6. Malnutrition at diagnosis of malignancy in childhood: common but mostly missed

   • D. E. Smith
   • M. C. G. Stevens
   • I. W. Booth

   Hematology/Oncology Pages: 318 - 322

7. Translocation t(8;16)(p11;p13) in neonatal acute monocytic leukaemia

   • T. Hanada
   • I. Ono
   • A. Ohtsu

   Hematology/Oncology Pages: 323 - 324

8. Autosomal recessive chronic granulomatous disease associated with 18q- syndrome and end-stage renal failure due to Henoch-Schönlein nephritis

   • J. Kimpen
   • R. Van Damme-Lombaerts
   • W. Proesmans

   Immunology/Allergology Pages: 325 - 326

9. Anti-neutrophil antibodies in patients with nutritional copper deficiency

   • S. Higuchi
   • A. Higashi
   • I. Matsuda

   Immunology/Allergology Pages: 327 - 330

10. Tuberculosis in children: a 13-year follow up of 1714 patients in a Belgian home care centre

    • M. Toppet
    • A. Malfroot
    • I. Dab

    Infectious Diseases Pages: 331 - 335

11. Congenital cutaneous candidiasis: Report of four cases and review of the literature

    • L. Almeida Santos
    • J. Beceiro
    • J. Quero

    Infectious Diseases Pages: 336 - 338

12. Reduced secretion of gastric inhibitory polypeptide in turner patients with impaired glucose tolerance

    • E. Heinze
    • J. Schlickenrieder
    • R. Ebert

    Medical Genetics Pages: 339 - 342

13. Calcinosis cutis, osteoma cutis, poikiloderma and skeletal abnormalities (COPS syndrome) — a new entity?

    • A. P. Oranje
    • S. M. P. F. de Muinck Keizer-Schrama
    • M. Meradji

    Medical Genetics Pages: 343 - 346

14. A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia

    • Y. Okano
    • R. C. Eisensmith
    • S. L. C. Woo

    Metabolic Diseases Pages: 347 - 352

15. N-Acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication

    • G. Schubiger
    • C. Bachmann
    • D. Schüpbach

    Metabolic Diseases Pages: 353 - 356

16. Combined conventional ventilation with high frequency oscillation in neonates

    • E. W. Hoskyns
    • A. D. Milner
    • I. E. Hopkin

    Neonatology Pages: 357 - 361

17. Intraoperative measurements of cerebral haemodynamics during ductus arteriosus ligation in preterm infants

    • E. M. Saliba
    • A. Chantepie
    • J. Laugier

    Neonatology Pages: 362 - 365

18. Aminophylline reduces cerebral blood flow in stable, preterm infants without affecting the visual evoked potential

    • O. Pryds
    • S. Schneider

    Neonatology Pages: 366 - 369

19. A variant of nephrogenic diabetes insipidus: V₂ receptor abnormality restricted to the kidney

    • N. Knoers
    • L. A. H. Monnens

    Nephrology Pages: 370 - 373

20. Haemostatic measurements in childhood nephrotic syndrome

    • A. T. H. Elidrissy
    • M. B. Abdurrahman
    • A. M. A. Gader

    Nephrology Pages: 374 - 378