1. The history of the glycogen storage diseases

   • J. Fernandes

   Classics in Pediatrics Pages: 423 - 424

2. Clinical manifestations of trisomy 4p syndrome

   • Sanjivan V. Patel
   • Hirut Dagnew
   • Ram S. Verma

   Review Pages: 425 - 431

3. Croup: A review

   • K. De Boeck

   Special Article Pages: 432 - 436

4. Treatment of patients with Ullrich-Turner syndrome with conventional doses of growth hormone and the combination with testosterone or oxandrolone: Effect on growth, IGF-I and IGFBP-3 concentrations

   • G. Haeusler
   • H. Frisch
   • T. Waldhör

   Endocrinology Pages: 437 - 444

5. Circadian growth hormone secretion in short multitransfused prepubertal children with thalassaemia major

   • G. Katzos
   • F. Harsoulis
   • K. Sava

   Endocrinology Pages: 445 - 449

6. Organ- and non-organ-specific auto-antibodies in children with hypopituitarism on growth hormone therapy

   • M. Maghnie
   • R. Lorini
   • F. Severi

   Endocrinology Pages: 450 - 453

7. Sleep apnoea in babies born after in vitro fertilization

   • H. Audiens
   • E. Denayer
   • Y. Vandenplas

   Growth/Development Pages: 454 - 457

8. Erythropoietin, erythropoesis and iron status in children after major surgical stress

   • Christoph Aufricht
   • Martina Ties
   • Ferdinand Haschke

   Hematology/Oncology Pages: 458 - 461

9. Tumour-induced rickets: A case report and review of the literature

   • B. Eyskens
   • W. Proesmans
   • M. Hoogmartens

   Hematology/Oncology Pages: 462 - 468

10. Fulminant liver failure in a 12-year-old girl with sickle cell anaemia: Favourable outcome after exchange transfusions

    • J. L. Stéphan
    • E. Merpit-Gonon
    • F. Freycon

    Hematology/Oncology Pages: 469 - 471

11. The changing presentations of meningococcal disease

    • F. A. I. Riordan
    • O. Marzouk
    • C. A. Hart

    Infectious Diseases Pages: 472 - 474

12. Acute post-streptococcal polymyalgia: Two new cases with a review of the literature

    • A. Venuta
    • P. Ferrari
    • L. Laudizi

    Infectious Diseases Pages: 475 - 476

13. Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus

    • D. Kotzot
    • F. Bernasconi
    • A. Schinzel

    Medical Genetics Pages: 477 - 482

14. Bone mineralisation in type 1 glycogen storage disease

    • Philip J. Lee
    • Jatin S. Patel
    • Nicholas J. Bishop

    Metabolic Diseases Pages: 483 - 487

15. The long-term effect of a partial whey hydrolysate formula on the prophylaxis of atopic disease

    • Y. Vandenplas
    • B. Hauser
    • I. Dab

    Nutrition Pages: 488 - 494

16. New for the practitioner

    News Pages: 495 - 496

17. The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany

    • R. Santer
    • N. Gregersen
    • J. Schaub

    Letters to the Editors Pages: 497 - 497

18. Osteomyelitis as a complication of perinatal fracture of the clavicle

    • Paolo G. Valerio
    • Peter Harmsen

    Letters to the Editors Pages: 497 - 498

19. Maternal amalgam and prenatal mercury exposure

    • Stefan Halbach
    • Karl H. Summer
    • G. Drasch

    Letters to the Editors Pages: 498 - 499

20. Benign infantile familial convulsions

    • E. Hauser
    • R. Seidl
    • A. Lischka

    Letters to the Editors Pages: 499 - 500

21. Immune-complex disease: A link between viral infection and sudden infant death?

    • S. Ritz
    • J. Peters
    • H. Thomsen

    Letters to the Editors Pages: 500 - 501

22. The frequency of MCAD mutation (K329E) in the Finnish population

    • E. I. Schwartz
    • J. Ilonen
    • H. K. Åkerblom

    Letters to the Editors Pages: 501 - 501

23. Partial splenic embolization in a child with hereditary spherocytosis

    • M. Jiménez
    • C. Azcona
    • L. Sierrasesúmaga

    Letters to the Editors Pages: 501 - 502