Pyridoxine-dependent seizures, clinical and therapeutic aspects C. -A. HaenggeliE. GirardinL. Paunier Review Pages: 452 - 455
Reye syndrome or side-effects of anti-emetics? M. Casteels-Van Daele Medical Controversies Pages: 456 - 459
Growth hormone treatment of Turner syndrome patients with insufficient growth hormone response to pharmacological stimulation tests G. MassaM. Vanderschueren-LodeweyckxG. van Vliet Endocrinology Pages: 460 - 463
Calcitonin secretion in children with insulin-dependent diabetes mellitus G. SaggeseS. BertelloniP. Ghirri Endocrinology Pages: 464 - 467
Histiocytic cytophagic panniculitis: Report of a case in a 12-year-old girl J. Garcia-ConsuegraM. I. BarrioF. Contreras Hematology/Oncology Pages: 468 - 469
Persistence of parvovirus B19-DNA in blood of a child with severe combined immunodeficiency associated with chronic pure red cell aplasia M. GahrA. PekrunH. Eiffert Hematology/Oncology Pages: 470 - 472
AIDS cases in adolescents and young adults in Italy: Inferences from descriptive epidemiology A. E. TozziS. SalmasoD. Greco Immunology/Allergology Pages: 473 - 476
Successful bone marrow transplantation and treatment of BCG infection in two patients with severe combined immunodeficiency R. S. HeydermanG. MorganS. Strobel Immunology/Allergology Pages: 477 - 480
Neutrophil chemotaxis in infants delivered by caesarean section A. GasparoniG. ChiricoG. Rondini Immunology/Allergology Pages: 481 - 482
Control of proven pulmonary and suspected CNS aspergillus infection with itraconazole in a patient with chronic granulomatous disease S. KloßA. SchusterV. Wahn Infectious Diseases Pages: 483 - 485
The cardio-facio-cutaneous syndrome: report of a patient and review of the literature A. BottaniI. HammererA. Schinzel Medical Genetics Pages: 486 - 488
Medullary sponge kidneys and unilateral Wilms tumour in a child with Beckwith-Wiedemann syndrome R. BeetzO. SchoferP. Gutjahr Medical Genetics Pages: 489 - 492
Maternal phenylketonuria syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation A. Superti-FurgaB. SteinmannR. Gitzelmann Metabolic Diseases Pages: 493 - 497
Pellagra with colitis due to a defect in tryptophan metabolism P. T. ClaytonN. A. BridgesD. A. Bender Metabolic Diseases Pages: 498 - 502
Effects of dopamine infusion on plasma catecholamines in preterm and term newborn infants H. StopfkuchenK. RackéK. Vogel Neonatology Pages: 503 - 506
Can high-dose immunoglobulin therapy be indicated in neonatal rhesus haemolysis? S. KuboT. ArigaT. Ishii Neonatology Pages: 507 - 508
Epoetin alfa in anaemic children or adolescents on regular dialysis M. G. BianchettiI. HämmerliO. H. Oetliker Nephrology/Urology Pages: 509 - 512
High serum aluminium levels and acute reversible encephalopathy in a 4-year-old boy with acute renal failure A. MorenoP. DomínguezA. Ballabriga Nephrology/Urology Pages: 513 - 514
Significance of ultrasound appearances in the neurological development and cognitive abilities of preterm infants at 5 years C. L. FawerA. Calame Neuropediatrics Pages: 515 - 520
Colour-flow-mapping in patients with ventricular septal defect C. -F. WippermannD. SchranzE. Trowitzsch Letters to the Editors Pages: 527 - 527
The 68th Annual General Meeting of the Scottish Paediatric Society A. G. M. Campbell Abstracts Pages: 528 - 532
