Clinical manifestations of trisomy 4p syndrome Sanjivan V. PatelHirut DagnewRam S. Verma Review Pages: 425 - 431
Treatment of patients with Ullrich-Turner syndrome with conventional doses of growth hormone and the combination with testosterone or oxandrolone: Effect on growth, IGF-I and IGFBP-3 concentrations G. HaeuslerH. FrischT. Waldhör Endocrinology Pages: 437 - 444
Circadian growth hormone secretion in short multitransfused prepubertal children with thalassaemia major G. KatzosF. HarsoulisK. Sava Endocrinology Pages: 445 - 449
Organ- and non-organ-specific auto-antibodies in children with hypopituitarism on growth hormone therapy M. MaghnieR. LoriniF. Severi Endocrinology Pages: 450 - 453
Sleep apnoea in babies born after in vitro fertilization H. AudiensE. DenayerY. Vandenplas Growth/Development Pages: 454 - 457
Erythropoietin, erythropoesis and iron status in children after major surgical stress Christoph AufrichtMartina TiesFerdinand Haschke Hematology/Oncology Pages: 458 - 461
Tumour-induced rickets: A case report and review of the literature B. EyskensW. ProesmansM. Hoogmartens Hematology/Oncology Pages: 462 - 468
Fulminant liver failure in a 12-year-old girl with sickle cell anaemia: Favourable outcome after exchange transfusions J. L. StéphanE. Merpit-GononF. Freycon Hematology/Oncology Pages: 469 - 471
The changing presentations of meningococcal disease F. A. I. RiordanO. MarzoukC. A. Hart Infectious Diseases Pages: 472 - 474
Acute post-streptococcal polymyalgia: Two new cases with a review of the literature A. VenutaP. FerrariL. Laudizi Infectious Diseases Pages: 475 - 476
Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus D. KotzotF. BernasconiA. Schinzel Medical Genetics Pages: 477 - 482
Bone mineralisation in type 1 glycogen storage disease Philip J. LeeJatin S. PatelNicholas J. Bishop Metabolic Diseases Pages: 483 - 487
The long-term effect of a partial whey hydrolysate formula on the prophylaxis of atopic disease Y. VandenplasB. HauserI. Dab Nutrition Pages: 488 - 494
The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany R. SanterN. GregersenJ. Schaub Letters to the Editors Pages: 497 - 497
Osteomyelitis as a complication of perinatal fracture of the clavicle Paolo G. ValerioPeter Harmsen Letters to the Editors Pages: 497 - 498
Maternal amalgam and prenatal mercury exposure Stefan HalbachKarl H. SummerG. Drasch Letters to the Editors Pages: 498 - 499
Benign infantile familial convulsions E. HauserR. SeidlA. Lischka Letters to the Editors Pages: 499 - 500
Immune-complex disease: A link between viral infection and sudden infant death? S. RitzJ. PetersH. Thomsen Letters to the Editors Pages: 500 - 501
The frequency of MCAD mutation (K329E) in the Finnish population E. I. SchwartzJ. IlonenH. K. Åkerblom Letters to the Editors Pages: 501 - 501
Partial splenic embolization in a child with hereditary spherocytosis M. JiménezC. AzconaL. Sierrasesúmaga Letters to the Editors Pages: 501 - 502