Familial glucocorticoid deficiency with achalasia of the cardia associated with mixed neuropathy, long-tract degeneration and mild dementia D. B. GrantD. B. DungerK. Hyland Endocrinology Pages: 85 - 89
Correlation of hepatitis B virus, hepatitis D virus and human immunodeficiency virus type I infection markers in hepatitis B surface antigen positive haemophiliacs and patients without haemophilia with clinical and histopathological outcome of hepatitis N. WagnerH. W. RotthauweH. H. Brackmann Gastroenterology/Hepatology Pages: 90 - 94
Thymic rebound following successful chemotherapy of B-lymphoma in an adolescent boy K. LeibundgutU. WilliH. -J. Plüss Hematology Pages: 95 - 97
Isotype composition of antibodies to streptococcus group B type III polysaccharide and to tetanus toxoid in maternal, cord blood sera and in breast milk T. LagergårdK. ThiringerB. Trollfors Immunology/Allergology Pages: 98 - 102
Recombinant human interferon-γ treatment in severe leucocyte adhesion deficiency R. S. WeeningR. G. M. BrediusD. Roos Immunology/Allergology Pages: 103 - 107
Mutations of the cystic fibrosis gene locus within the population of the Northwest of England M. SuperM. J. Schwarz Medical Genetics Pages: 108 - 111
Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy T. VoitE. Neuen-JacobM. Cremer Medical Genetics Pages: 112 - 116
Clinical recognition of patients affected by a peroxisomal disorder: A retrospective study in 40 patients A. C. TheilR. B. H. SchutgensH. S. A. Heymans Metabolic Diseases Pages: 117 - 120
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency E. BertiniC. Dionisi-ViciS. DiDonato Metabolic Diseases Pages: 121 - 126
Clinical and biochemical observations in a patient with combined Pompe disease and cblC mutation F. A. WijburgD. S. RosenblattR. B. H. Schutgens Metabolic Diseases Pages: 127 - 131
Increased intracranial pressure in a neonate with citrullinaemia J. -L. WayenbergD. VermeylenA. Pardou Metabolic Diseases Pages: 132 - 133
Dexamethasone and hypertension in preterm infants A. GreenoughE. F. EmeryH. R. Gamsu Neonatology Pages: 134 - 135
Non-invasive blood pressure monitoring in preterm infants receiving intensive care E. F. EmeryA. Greenough Neonatology Pages: 136 - 139
Effectiveness of early prednisone treatment in preventing the development of nephropathy in anaphylactoid purpura F. MollicaS. LiVoltiG. Russo Nephrology/Urology Pages: 140 - 144
Yersinia enterocolitica mesenteric adenitis in a thalassaemic adolescent P. CianciulliG. TruaC. Chiesa Letters to the Editors Pages: 145 - 146
Bowen syndrome: Congenital glaucoma, flexion contracture of fingers and facial dysmorphism without peroxisomal abnormalities T. Billette de VillemeurG. BijaouiJ. M. Richardet Letters to the Editors Pages: 146 - 147
Low frequency of high level Shiga-like toxin production in enteropathogenicEscherichia coli 0 serogroups N. CimolaiC. Trombley Letters to the Editors Pages: 147 - 147
Effect of a long-term methionyl growth hormone treatment on growth hormone releasing hormone-induced growth hormone secretion in patients with constitutional growth delay A. SartorioA. ContiG. Faglia Letters to the Editors Pages: 148 - 149
Human milk T lymphocytes are mostly HML-1-positive cells A. BertottoG. CastellucciR. Vaccaro Letters to the Editors Pages: 150 - 150
Permanent neonatal diabetes mellitus: Lack of diabetic complications after a 20-year follow up H. Dorchy Letters to the Editors Pages: 151 - 151
The use of midazolam in the preterm neonate J. N. van den AnkerP. J. J. Sauer Letters to the Editors Pages: 152 - 152