The Marfan syndrome —analysis of growth and cardiovascular manifestation U. VetterR. MayerhoferA. A. Schmaltz Cardiology Pages: 452 - 456
An atypical paediatric case of malignant atrophic papulosis (Köhlmeier-Degos disease) A. BarabinoF. PesceA. Giampalmo Dermatology Pages: 457 - 458
Serum immunoreactive erythropoietin of children in health and disease K. -U. EckardtW. HartmannA. Kurtz Hematology/Oncology Pages: 459 - 464
Brittle cornea syndrome: An heritable connective tissue disorder distinct from Ehlers-Danlos syndrome type VI and fragilitas oculi, with spontaneous perforations of the eye, blue sclerae, red hair, and normal collagen lysyl hydroxylation P. M. RoyceB. SteinmannA. Kohlschuetter Medical Genetics Pages: 465 - 469
Mental retardation syndrome with renal concentration deficiency and intracerebral calcification O. SchoferR. BeetzJ. Spranger Medical Genetics Pages: 470 - 474
Ring chromosome 7: Report of the fifth case G. M. CaramiaA. BaronciniA. Forabosco Medical Genetics Pages: 475 - 476
Nephrosis in two siblings with infantile sialic acid storage disease W. SperlW. GruberE. Paschke Metabolic Diseases Pages: 477 - 482
Non-invasive31P magnetic resonance spectroscopy revealed McArdle disease in an asymptomatic child R. GruetterP. KaelinB. Werner Metabolic Diseases Pages: 483 - 486
Deficiency of the α and β subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death W. SperlW. RuitenbeekJ. A. J. M. Bakkeren Metabolic Diseases Pages: 487 - 492
Risk factors for fatal pulmonary interstitial emphysema in neonates C. MorisotN. KacetP. Lequien Neonatology Pages: 493 - 495
Pulmonary hypoplasia secondary to oligohydramnios with very premature rupture of fetal membranes D. TibboelJ. L. J. GaillardH. C. S. Wallenburg Neonatology Pages: 496 - 499
Priapism and Fabry disease: A case report J. García-ConsuegraM. PadrónJ. Ramos Nephrology/Urology Pages: 500 - 501
Primitive megalencephaly in children: Natural history, medium term prognosis with special reference to external hydrocephalus B. LaubscherT. DeonnaG. van Melle Neuropediatrics Pages: 502 - 507
Fatty acid composition of phospholipids of plasma and of mononuclear blood cells in children with allergic asthma and the influence of glucocorticoids M. GrieseN. SchurB. Biggemann Pneumology Pages: 508 - 512
DNA testing for Huntington disease results in a modification of risk and not diagnosis of disease M. BlochM. R. HaydenM. Schömig-Spingler Letters to the Editors Pages: 513 - 513
The 67th Annual General Meeting of the Scottish Paediatric Society Eric Coleman Abstracts Pages: 514 - 516
