Practical interest in the detection of functional abnormalities in infants and children with lung disease R. Kraemer Review Pages: 382 - 386
Withdrawal of a mumps vaccine: Reasons and impacts H. -J. SchmittM. JustA. Neiss Annotation Pages: 387 - 388
Topical application of 1,25-dihydroxyvitamin D3 (calcitriol) is an effective and reliable therapy to cure skin lesions in psoriatic children G. SaggeseG. FedericoR. Battini Dermatology Pages: 389 - 392
Failure to improve height prediction in short-stature pubertal adolescents by inhibiting puberty with luteinizing hormone-releasing hormone analogue D. LindnerJ. C. JobJ. L. Chaussain Endocrinology Pages: 393 - 396
Pericardial effusion as a sign of acquired hypothyroidism in children with Down syndrome E. A. WerderT. TorresaniU. Hunziker Endocrinology Pages: 397 - 398
Pituitary stalk thickening with diabetes insipidus preceding typical manifestations of Langerhans cell histiocytosis in children S. SchmittW. WichmannE. J. Schoenle Hematology/Oncology Pages: 399 - 401
A kindred with Griscelli disease: Spectrum of neurological involvement H. HurvitzR. GillisE. Okon Immunology/Allergology Pages: 402 - 405
IgG4 deficiency with Rothmund-Thomson syndrome: A case report M. KubotaM. YasunagaC. Nishigori Immunology/Allergology Pages: 406 - 408
B-cell and T-regulatory cell dysfunction in six Chinese children with hypogammaglobulinaemia B. M. JonesY. L. LauK. L. Wong Immunology/Allergology Pages: 409 - 413
Detection ofBorrelia burgdorferi by nested polymerase chain reaction in cerebrospinal fluid and urine of children with neuroborreliosis H. -I. HuppertzH. SchmidtH. Karch Infectious Diseases Pages: 414 - 417
Association of hiatus hernia with asplenia syndrome J. -K. WangM. -H. ChangH. -C. Lue Medical Genetics Pages: 418 - 420
Hypogonadism in a patient with balanced X/18 translocation and pituitary hormone deficiency D. LarizzaP. MaraschioP. Sampaolo Medical Genetics Pages: 424 - 427
An unusual patient with the neonatal Marfan phenotype and mitochondrial complex I deficiency J. ChristodoulouR. Petrova-BenedictJ. T. R. Clarke Medical Genetics Pages: 428 - 432
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency—diagnosis, plasma carnitine fractions and management in a further patient R. MooreJ. F. T. GlasgowK. Carpenter Metabolic Diseases Pages: 433 - 436
Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intolerance M. DiRoccoG. GaribottoC. Borrone Metabolic Diseases Pages: 437 - 440
Holocarboxylase synthetase deficiency: Early diagnosis and management of a new case A. FuchshuberT. SuormalaE. R. Baumgartner Metabolic Diseases Pages: 446 - 449
Polyposis of the gallbladder associated with metachromatic leukodystrophy M. RiesK. -H. Deeg Metabolic Diseases Pages: 450 - 451
Pre- and post-operative MRI study of an aneurysm of the right brachiocephalic artery with tracheal compression A. LivolsiL. DonatoB. Eisenmann Letters to the Editors Pages: 457 - 457
Human immunodeficiency virus-type 1 screening in pregnancy: The magic wand to prevent perinatal infection in Europe? L. GalliM. de MartinoA. Vierucci Letters to the Editors Pages: 458 - 458
Flumazenil reverses diazepam-induced neonatal apnoea and hypotonia A. M. ConeS. NadelB. Sweeney Letters to the Editors Pages: 458 - 459
Complement activation in neonatal disease E. P. ZilowL. Schrod Letters to the Editors Pages: 459 - 460
Pentoxifylline treatment of persistent pulmonary hypertension of newborn R. Lauterbach Letters to the Editors Pages: 460 - 460
