Guidelines for neonatal screening programmes for congenital hypothyroidism Working group on congenital hypothyroidism of the European Society for Paediatric EndocrinologyA. GrütersJ. E. Toublanc Special Article Pages: 974 - 975
Extended deep vein and inferior vena cava thrombosis in a 15-year-old boy: Successful lysis with recombinant tissue-type plasminogen activator 2 weeks after onset of symptoms T. RosenbaumS. RammosU. Göbel Cardiology Pages: 978 - 980
Liposomal amphotericin-B (AmBisome) for treatment of cutaneous widespread candidosis in an infant with methylmalonic acidaemia S. StöcklerH. LacknerW. Müller Dermatology Pages: 981 - 983
Circulating immunoreactive growth hormone releasing hormone concentrations and growth hormone response to growth hormone releasing hormone in short children P. J. Tapanainen Endocrinology Pages: 984 - 989
Hypergalactosaemia in a patient with portal-hepatic venous and hepatic arterio-venous shunts detected by neonatal screening T. MatsumotoR. OkanoD. Amano Gastroenterology/Hepatology Pages: 990 - 992
Pubertal development in thalassaemic patients after allogenic bone marrow transplantation V. De SanctisM. GalimbertiC. Vullo Hematology/Oncology Pages: 993 - 997
Effect of interleukin 2 on intractable herpes virus infection and chronic eczematoid dermatitis in a patient with Wiskott-Aldrich syndrome H. AzumaH. SakataA. Okuno Immunology/Allergology Pages: 998 - 1000
Recurrent wheezing in children with respiratory syncytial virus (RSV) bronchiolitis in Qatar V. M. OsundwaS. T. DawodM. Ehlayel Infectious Diseases Pages: 1001 - 1003
Neonatal suppurative parotitis: A vanishing disease? A. ÇobanZ InceG. Can Infectious Diseases Pages: 1004 - 1005
Cystic fibrosis: The ΔF508 mutation does not lead to an exceptionally severe phenotype. A cohort study G. BorgoP. GaspariniP. F. Pignatti Medical Genetics Pages: 1006 - 1011
White matter abnormalities in patients with treated hyperphenylalaninaemia: Magnetic resonance relaxometry and proton spectroscopy findings U. BickK. UllrichU. Wendel Metabolic Disease Pages: 1012 - 1020
Contribution of odd-numbered fatty acid oxidation to propionate production in neonates with methylmalonic an propionic acidaemias U. WendelR. ZassD. Leupold Metabolic Disease Pages: 1021 - 1023
Correlations between radiological and cytological findings in early development of bronchopulmonary dysplasia G. NoackW. MortenssonR. Nilsson Neonatology Pages: 1024 - 1029
Results of parenchymal and angiographic magnetic resonance imaging and neuropsychological testing of children after stroke as neonates W. KoelfenM. FreundCh. Schultze Neuropediatrics Pages: 1030 - 1035
Protein quality of human milk fortifier in low birth weight infants: Effects on growth and plasma amino acid profiles G. BoehmM. BorteI. Minoli Nutrition Pages: 1036 - 1039
Carbamazepine hypersensitivity and rickettsiosis mimicking Kawasaki disease S. ParhaA. GaroufiTh. Karpathios Pharmacology Pages: 1040 - 1041
Trends in hospitalization among asthmatic children in Finland from 1972 to 1986 T. TuuponenT. KeistinenS. -L. Kivelä Pneumology Pages: 1042 - 1044
Neuro-ophthalmological manifestations of tick-borne borreliosis: a case report K. AlbermannW. BlunckH. Helwig Letters to the Editors Pages: 1046 - 1047
Bloody nipple discharge in a 3-year-old girl K. U. MenkenC. Roll Letters to the Editors Pages: 1047 - 1047
Facilitation of hyperphenylalaninaemia phenotype assessment by genotype analysis D. S. KoneckiS. Schweitzer-KrantzU. Lichter-Konecki Letters to the Editors Pages: 1048 - 1049
