Spontaneous pneumomediastinum in children F. G. A. VersteeghI. A. J. M. Broeders Review Pages: 304 - 307
Persistent hyperthyrotropinaemia since the neonatal period in clinically euthyroid children L. A. TyfieldS. S. A. AbusrewilD. C. L. Savage Endocrinology Pages: 308 - 309
Abnormal results of biochemical liver function tests in breast-fed infants with prolonged indirect hyperbilirubinaemia Y. TazawaD. AbukawaM. Yamada Gastroenterology/Hepatology Pages: 310 - 313
Coombs-positive giant cell hepatitis of infancy: effect of steroids and azathioprine therapy B. BrichardE. SokalG. Cornu Gastroenterology/Hepatology Pages: 314 - 317
Malnutrition at diagnosis of malignancy in childhood: common but mostly missed D. E. SmithM. C. G. StevensI. W. Booth Hematology/Oncology Pages: 318 - 322
Translocation t(8;16)(p11;p13) in neonatal acute monocytic leukaemia T. HanadaI. OnoA. Ohtsu Hematology/Oncology Pages: 323 - 324
Autosomal recessive chronic granulomatous disease associated with 18q- syndrome and end-stage renal failure due to Henoch-Schönlein nephritis J. KimpenR. Van Damme-LombaertsW. Proesmans Immunology/Allergology Pages: 325 - 326
Anti-neutrophil antibodies in patients with nutritional copper deficiency S. HiguchiA. HigashiI. Matsuda Immunology/Allergology Pages: 327 - 330
Tuberculosis in children: a 13-year follow up of 1714 patients in a Belgian home care centre M. ToppetA. MalfrootI. Dab Infectious Diseases Pages: 331 - 335
Congenital cutaneous candidiasis: Report of four cases and review of the literature L. Almeida SantosJ. BeceiroJ. Quero Infectious Diseases Pages: 336 - 338
Reduced secretion of gastric inhibitory polypeptide in turner patients with impaired glucose tolerance E. HeinzeJ. SchlickenriederR. Ebert Medical Genetics Pages: 339 - 342
Calcinosis cutis, osteoma cutis, poikiloderma and skeletal abnormalities (COPS syndrome) — a new entity? A. P. OranjeS. M. P. F. de Muinck Keizer-SchramaM. Meradji Medical Genetics Pages: 343 - 346
A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia Y. OkanoR. C. EisensmithS. L. C. Woo Metabolic Diseases Pages: 347 - 352
N-Acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication G. SchubigerC. BachmannD. Schüpbach Metabolic Diseases Pages: 353 - 356
Combined conventional ventilation with high frequency oscillation in neonates E. W. HoskynsA. D. MilnerI. E. Hopkin Neonatology Pages: 357 - 361
Intraoperative measurements of cerebral haemodynamics during ductus arteriosus ligation in preterm infants E. M. SalibaA. ChantepieJ. Laugier Neonatology Pages: 362 - 365
Aminophylline reduces cerebral blood flow in stable, preterm infants without affecting the visual evoked potential O. PrydsS. Schneider Neonatology Pages: 366 - 369
A variant of nephrogenic diabetes insipidus: V2 receptor abnormality restricted to the kidney N. KnoersL. A. H. Monnens Nephrology Pages: 370 - 373
Haemostatic measurements in childhood nephrotic syndrome A. T. H. ElidrissyM. B. AbdurrahmanA. M. A. Gader Nephrology Pages: 374 - 378