Hirschsprung disease: Paternal transmission to a son H. SkopnikU. BeudtM. Habedank Gastroenterology/Hepatology Pages: 467 - 468
A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease T. ArigaY. SakiyamaS. Matsumoto Hematology/Oncology Pages: 469 - 472
Anti-neutrophil cytoplasmic auto-antibodies-associated vasculitis with pulmonary and renal involvement G. Pintos-MorellA. Roca-ComasJ. Prats Immunology/Allergology Pages: 473 - 475
Immunological responses in an infant after cyclosporine A exposure during pregnancy R. BaarsmaW. A. Kamps Immunology/Allergology Pages: 476 - 477
Acellular pertussis diphtheria-tetanus-pertussis vaccine containing separately purified pertussis toxoid, filamentous haemagglutinin and 69 kDa outer membrane protein as a booster in children G. KanraM. CeyhanH. Bogaerts Infectious Diseases Pages: 478 - 483
Early detection of IgA specific antibodies in HIV-1 infected children by peptide-ELISA and peptide time-resolved fluoro-immunoassay V. LombardiM. CanigliaP. Rossi Infectious Diseases Pages: 484 - 489
Association of hepatitis C virus infection with chronic liver disease in paediatric cancer patients F. M. FinkS. Höcker-SchulzH. Gadner Infectious Diseases Pages: 490 - 492
Isolation of adenovirus type 11 from the brain of a neonate with pneumonia and encephalitis T. OsamuraR. MizutaS. Fushiki Infectious Diseases Pages: 496 - 499
Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): A follow-up study A. FoisL. CalistriM. Vanni Medical Genetics Pages: 500 - 504
Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome) R. E. BrennerU. VetterW. M. Teller Medical Genetics Pages: 505 - 508
Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism Á. HaraldssonC. J. A. M. van der BurgtG. B. A. Stoelinga Medical Genetics Pages: 509 - 512
Myoadenylate deaminase deficiency with severe rhabdomyolysis F. A. M. BaumeisterM. GrossR. Eife Metabolic Diseases Pages: 513 - 515
Effect of chronic lung disease on blood pressure levels at follow up A. GreenoughE. F. Emery Neonatology Pages: 516 - 518
Diminished cord blood lymphocytel-selectin expression in neonatal bacterial infection C. BührerU. LuxenburgerM. Obladen Neonatology Pages: 519 - 522
Primary vesicoureteral reflux in infants with a dilated fetal urinary tract E. RingP. PetritschG. Fueger Nephrology/Urology Pages: 523 - 525
Hypothalamic dysfunction in a child: A distinct syndrome? F. ProulxM. L. WeberM. Delisle Neuropediatrics Pages: 526 - 529
Ceftriaxone-bilirubin-albumin interactions in the neonate: An in vivo study E. MartinA. FanconiR. Brodersen Pharmacology Pages: 530 - 534
Beneficial effect of sodium dichloroacetate in muscle cytochrome C oxidase deficiency A. B. BurlinaO. MilanesiS. Di Mauro Letters to the Editors Pages: 537 - 537
Insufficient ketoconazole concentrations in preterm infants with fungal infections J. N. van den AnkerR. A. van LingenP. J. J. Sauer Letters to the Editors Pages: 538 - 538
Is liver involvement of beta thalassaemic children related to the presence of hepatitis C virus antibodies? Ş. ÖzsoyluM. RestiA. Vierucci Letters to the Editors Pages: 538 - 539
Congenital atresia of left coronary ostium K. HaradaT. ItoG. Takada Letters to the Editors Pages: 539 - 540
Klinefelter syndrome associated with juvenile hypothyroidism due to chronic thyroiditis T. Kondo Letters to the Editors Pages: 540 - 540
Neonatal necrotizing enterocolitis and co-existing defect of the intestinal musculature B. HöhmannM. HolzwarthW. Krautzberger Letters to the Editors Pages: 540 - 541
Coma in a neonate following single intranasal dose of xylometazoline C. DunnM. GauthierP. Gaudreault Letters to the Editors Pages: 541 - 541
The 70th Annual General Meeting of the Scottish Paediatric Society James Syme Abstracts Pages: 542 - 544
