Jürgen Spranger: On the occasion of his 60th birthday Hans-Rudolf Wiedemann Announcement Pages: 219 - 219
Diffuse infantile haemangiomatosis: clinicopathological features and management problems in five fatal cases R. W. ByardP. E. BurrowsM. M. Silver Hematology/Oncology Pages: 224 - 227
Mega-dose intravenous methylprednisone for the treatment of onyalai: a case report S. ÖzsoyluG. Ertürk Hematology/Oncology Pages: 228 - 229
Lymphocyte subsets in whole blood and isolated mononuclear leucocytes of healthy infants and children N. RemyM. OberreitU. Wahn Immunology/Allergology Pages: 230 - 233
IgG2 deficiency in children with human immunodeficiency virus infection P. BartmannI. Grosch-WörnerB. H. Belohradsky Immunology/Allergology Pages: 234 - 237
Effects of short-term administration of human chorionic gonadotropin on immune functions in cryptorchid children M. MaghnieA. ValtortaF. Severi Immunology/Allergology Pages: 238 - 241
Severe pulmonary vascular occlusive disease following bone marrow transplantation in Omenn syndrome C. BrückmannW. LindnerB. H. Belohradsky Immunology/Allergology Pages: 242 - 245
New observations on midline defects: Coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders J. R. BierichM. ChristieA. S. Martinez Medical Genetics Pages: 246 - 249
Cystic fibrosis and Helicobacter pylori gastritis, megaloblastic anaemia, subnormal mentality and minor anomalies in two siblings: a new syndrome? M. M. LubaniQ. A. Al-SalehM. H. Kalaoui Medical Genetics Pages: 253 - 255
Prenatal deletion detection in a sporadic case of Duchenne muscular dystrophy without genotype information from the affected individual F. PeinemannM. WagnerJ. Reiss Medical Genetics Pages: 256 - 258
Renal tubular dysfunction in methylmalonic acidaemia C. T. D'AngioM. J. DillonJ. V. Leonard Metabolic Diseases Pages: 259 - 263
Cystic fibrosis presenting with recurrent vomiting and metabolic alkalosis P. M. MathewJ. A. HamdanH. Nazer Metabolic Diseases Pages: 264 - 266
Breast mild jaundice: Natural history, familial incidence and late neurodevelopmental outcome of the infant E. GrunebaumJ. AmirI. Varsano Neonatology Pages: 267 - 270
First day serum creatine kinase BB isoenzyme in high-risk infants R. A. PrimhakE. Simmonds Neonatology Pages: 271 - 273
Clinical usefulness of high intensity green light phototherapy in the treatment of neonatal jaundice M. AmatoD. Inaebnit Neonatology Pages: 274 - 276
Early onset neonatal sepsis with Campylobacter jejuni: A case report R. KrishnaswamyP. SasidharanY. Abu Osba Neonatology Pages: 277 - 278
Haemolytic uraemic syndrome in the defined population of Northeast of Scotland I. A. Abu-ArafehP. J. SmailI. A. Auchterlonie Nephrology Pages: 279 - 281
Brain abscess in childhood-long-term experiences C. AebiF. KaufmannU. B. Schaad Neuropediatrics Pages: 282 - 286
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy J. KapplerR. W. E. WattsV. Gieselmann Neuropediatrics Pages: 287 - 290
The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency C. JakobsF. StellaardP. Rovers Letter to the Editors Pages: 291 - 291