1. Jürgen Spranger: On the occasion of his 60th birthday

   • Hans-Rudolf Wiedemann

   Announcement Pages: 219 - 219

2. Balloon occlusion aortography

   • T. Ino
   • S. Shimazaki
   • Y. Hosoda

   Review Pages: 220 - 223

3. Diffuse infantile haemangiomatosis: clinicopathological features and management problems in five fatal cases

   • R. W. Byard
   • P. E. Burrows
   • M. M. Silver

   Hematology/Oncology Pages: 224 - 227

4. Mega-dose intravenous methylprednisone for the treatment of onyalai: a case report

   • S. Özsoylu
   • G. Ertürk

   Hematology/Oncology Pages: 228 - 229

5. Lymphocyte subsets in whole blood and isolated mononuclear leucocytes of healthy infants and children

   • N. Remy
   • M. Oberreit
   • U. Wahn

   Immunology/Allergology Pages: 230 - 233

6. IgG2 deficiency in children with human immunodeficiency virus infection

   • P. Bartmann
   • I. Grosch-Wörner
   • B. H. Belohradsky

   Immunology/Allergology Pages: 234 - 237

7. Effects of short-term administration of human chorionic gonadotropin on immune functions in cryptorchid children

   • M. Maghnie
   • A. Valtorta
   • F. Severi

   Immunology/Allergology Pages: 238 - 241

8. Severe pulmonary vascular occlusive disease following bone marrow transplantation in Omenn syndrome

   • C. Brückmann
   • W. Lindner
   • B. H. Belohradsky

   Immunology/Allergology Pages: 242 - 245

9. New observations on midline defects: Coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders

   • J. R. Bierich
   • M. Christie
   • A. S. Martinez

   Medical Genetics Pages: 246 - 249

10. The Floating-Harbor syndrome

    • F. Majewski
    • H. -G. Lenard

    Medical Genetics Pages: 250 - 252

11. Cystic fibrosis and Helicobacter pylori gastritis, megaloblastic anaemia, subnormal mentality and minor anomalies in two siblings: a new syndrome?

    • M. M. Lubani
    • Q. A. Al-Saleh
    • M. H. Kalaoui

    Medical Genetics Pages: 253 - 255

12. Prenatal deletion detection in a sporadic case of Duchenne muscular dystrophy without genotype information from the affected individual

    • F. Peinemann
    • M. Wagner
    • J. Reiss

    Medical Genetics Pages: 256 - 258

13. Renal tubular dysfunction in methylmalonic acidaemia

    • C. T. D'Angio
    • M. J. Dillon
    • J. V. Leonard

    Metabolic Diseases Pages: 259 - 263

14. Cystic fibrosis presenting with recurrent vomiting and metabolic alkalosis

    • P. M. Mathew
    • J. A. Hamdan
    • H. Nazer

    Metabolic Diseases Pages: 264 - 266

15. Breast mild jaundice: Natural history, familial incidence and late neurodevelopmental outcome of the infant

    • E. Grunebaum
    • J. Amir
    • I. Varsano

    Neonatology Pages: 267 - 270

16. First day serum creatine kinase BB isoenzyme in high-risk infants

    • R. A. Primhak
    • E. Simmonds

    Neonatology Pages: 271 - 273

17. Clinical usefulness of high intensity green light phototherapy in the treatment of neonatal jaundice

    • M. Amato
    • D. Inaebnit

    Neonatology Pages: 274 - 276

18. Early onset neonatal sepsis with Campylobacter jejuni: A case report

    • R. Krishnaswamy
    • P. Sasidharan
    • Y. Abu Osba

    Neonatology Pages: 277 - 278

19. Haemolytic uraemic syndrome in the defined population of Northeast of Scotland

    • I. A. Abu-Arafeh
    • P. J. Smail
    • I. A. Auchterlonie

    Nephrology Pages: 279 - 281

20. Brain abscess in childhood-long-term experiences

    • C. Aebi
    • F. Kaufmann
    • U. B. Schaad

    Neuropediatrics Pages: 282 - 286

21. Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy

    • J. Kappler
    • R. W. E. Watts
    • V. Gieselmann

    Neuropediatrics Pages: 287 - 290

22. The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency

    • C. Jakobs
    • F. Stellaard
    • P. Rovers

    Letter to the Editors Pages: 291 - 291

23. 27th Workshop for Pediatric Research

    • Werner Schröter

    Abstracts Pages: 292 - 301