1. Anton Oberniedermayr

   • H. -R. Wiedemann

   The Pioneers of Pediatric Medicine Pages: 77 - 77

2. β-thalassaemia: Molecular pathogenesis and clinical variability

   • A. E. Kulozik

   Review Pages: 78 - 84

3. Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia

   • D. B. Grant
   • D. B. Dunger
   • K. Hyland

   Endocrinology Pages: 85 - 89

4. Correlation of hepatitis B virus, hepatitis D virus and human immunodeficiency virus type I infection markers in hepatitis B surface antigen positive haemophiliacs and patients without haemophilia with clinical and histopathological outcome of hepatitis

   • N. Wagner
   • H. W. Rotthauwe
   • H. H. Brackmann

   Gastroenterology/Hepatology Pages: 90 - 94

5. Thymic rebound following successful chemotherapy of B-lymphoma in an adolescent boy

   • K. Leibundgut
   • U. Willi
   • H. -J. Plüss

   Hematology Pages: 95 - 97

6. Isotype composition of antibodies to streptococcus group B type III polysaccharide and to tetanus toxoid in maternal, cord blood sera and in breast milk

   • T. Lagergård
   • K. Thiringer
   • B. Trollfors

   Immunology/Allergology Pages: 98 - 102

7. Recombinant human interferon-γ treatment in severe leucocyte adhesion deficiency

   • R. S. Weening
   • R. G. M. Bredius
   • D. Roos

   Immunology/Allergology Pages: 103 - 107

8. Mutations of the cystic fibrosis gene locus within the population of the Northwest of England

   • M. Super
   • M. J. Schwarz

   Medical Genetics Pages: 108 - 111

9. Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy

   • T. Voit
   • E. Neuen-Jacob
   • M. Cremer

   Medical Genetics Pages: 112 - 116

10. Clinical recognition of patients affected by a peroxisomal disorder: A retrospective study in 40 patients

    • A. C. Theil
    • R. B. H. Schutgens
    • H. S. A. Heymans

    Metabolic Diseases Pages: 117 - 120

11. Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

    • E. Bertini
    • C. Dionisi-Vici
    • S. DiDonato

    Metabolic Diseases Pages: 121 - 126

12. Clinical and biochemical observations in a patient with combined Pompe disease and cblC mutation

    • F. A. Wijburg
    • D. S. Rosenblatt
    • R. B. H. Schutgens

    Metabolic Diseases Pages: 127 - 131

13. Increased intracranial pressure in a neonate with citrullinaemia

    • J. -L. Wayenberg
    • D. Vermeylen
    • A. Pardou

    Metabolic Diseases Pages: 132 - 133

14. Dexamethasone and hypertension in preterm infants

    • A. Greenough
    • E. F. Emery
    • H. R. Gamsu

    Neonatology Pages: 134 - 135

15. Non-invasive blood pressure monitoring in preterm infants receiving intensive care

    • E. F. Emery
    • A. Greenough

    Neonatology Pages: 136 - 139

16. Effectiveness of early prednisone treatment in preventing the development of nephropathy in anaphylactoid purpura

    • F. Mollica
    • S. LiVolti
    • G. Russo

    Nephrology/Urology Pages: 140 - 144

17. Yersinia enterocolitica mesenteric adenitis in a thalassaemic adolescent

    • P. Cianciulli
    • G. Trua
    • C. Chiesa

    Letters to the Editors Pages: 145 - 146

18. Bowen syndrome: Congenital glaucoma, flexion contracture of fingers and facial dysmorphism without peroxisomal abnormalities

    • T. Billette de Villemeur
    • G. Bijaoui
    • J. M. Richardet

    Letters to the Editors Pages: 146 - 147

19. Low frequency of high level Shiga-like toxin production in enteropathogenicEscherichia coli 0 serogroups

    • N. Cimolai
    • C. Trombley

    Letters to the Editors Pages: 147 - 147

20. Effect of a long-term methionyl growth hormone treatment on growth hormone releasing hormone-induced growth hormone secretion in patients with constitutional growth delay

    • A. Sartorio
    • A. Conti
    • G. Faglia

    Letters to the Editors Pages: 148 - 149

21. Ascorbic acid and alkaptonuria

    • P. Kamoun
    • M. Coude
    • J. L. Guenet

    Letters to the Editors Pages: 149 - 149

22. Human milk T lymphocytes are mostly HML-1-positive cells

    • A. Bertotto
    • G. Castellucci
    • R. Vaccaro

    Letters to the Editors Pages: 150 - 150

23. Reye syndrome

    • G. Veereman-Wauters
    • R. Dimand

    Letters to the Editors Pages: 150 - 150

24. Permanent neonatal diabetes mellitus: Lack of diabetic complications after a 20-year follow up

    • H. Dorchy

    Letters to the Editors Pages: 151 - 151

25. The use of midazolam in the preterm neonate

    • J. N. van den Anker
    • P. J. J. Sauer

    Letters to the Editors Pages: 152 - 152