Criss-cross heart evaluated by colour Doppler echocardiography and magnetic resonance imaging H. IgarashiT. KuramatsuM. Yanagisawa Cardiology Pages: 523 - 525
Blue rubber-bled naevus syndrome: Report of a case with consumption coagulopathy complicated by manifest thrombosis W. J. D. HofhuisA. P. OranjeM. Sinaasappel Dermatology Pages: 526 - 528
Comparison of atrophic and goitrous auto-immune thyroiditis in children: Clinical, laboratory and TSH-receptor antibody studies N. MatsuuraJ. KonishiA. Okuno Endocrinology Pages: 529 - 533
Premature thelarche: A possible adverse effect of cimetidine treatment J. M. BosmanN. M. A. BaxJ. M. Wit Endocrinology Pages: 534 - 535
Growth hormone deficiency in children: Role of magnetic resonance imaging in assessing aetiopathogenesis and prognosis in idiopathic hypopituitarism C. PelliniB. di NataleG. Chiumello Endocrinology Pages: 536 - 541
Concurrence of transient asplenia and pure red cell aplasia M. F. OzkaynakJ. A. OrtegaJ. Miller Hematology/Oncology Pages: 542 - 544
Oral immunotherapy with grass pollen in enterosoluble capsules R. UrbanekK. H. BürgelinU. Wahn Immunology/Allergology Pages: 545 - 550
Increase of CALLA-positive stimulated lymphoid cells in transient erythroblastopenia of childhood S. LeuschnerS. Bödewaldt-RadzunM. Rister Immunology/Allergology Pages: 551 - 554
Three cases of neonatal herpes simplex virus infection presenting as fulminant hepatitis N. BenadorW. MannhardtS. Suter Infectious Diseases Pages: 555 - 559
Acute mastoiditis: Clinical, microbiological, and therapeutic aspects D. NadalP. HerrmannA. Fanconi Infectious Diseases Pages: 560 - 564
Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): Report of three additional cases E. JaeggiC. KindR. Morger Medical Genetics Pages: 565 - 566
Autistic disorder in Sotos syndrome: A case report J. D. MorrowB. Y. WhitmanP. J. Accardo Medical Genetics Pages: 567 - 569
The effect of fasting hyperinsulinaemia on physical fitness in obese children D. MolnàrJ. Pòrszàsz Metabolic Diseases Pages: 570 - 573
Biochemical and clinical observations in four patients with fructose-1,6-diphosphatase deficiency P. BührdelH. -J. BöhmeL. Didt Metabolic Diseases Pages: 574 - 576
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: Report of two siblings C. CatzeflisC. BachmannG. Délèze Metabolic Diseases Pages: 577 - 581
Symmetrical necrosis of the basal ganglia in methylmalonic acidaemia A. M. RoodhooftE. R. BaumgartnerK. J. Van Acker Metabolic Diseases Pages: 582 - 584
Very early prolonged premature rupture of membranes and survival J. H. HoekstraR. de Boer Neonatology Pages: 585 - 586
Impact of hyperbilirubinaemia and transient mother-child separation in the neonatal period on mother-child attachment in the 1st year of life A. SchedleH. S. Fricker Neonatology Pages: 587 - 591
Pain symptoms in an adolescent Italian population G. MagniG. CantonL. Gallimberti Psychology/Child Psychiatry Pages: 592 - 593
Therapeutic attempts in sulphite oxidase deficiency P. KamounP. Tardy Letters to the Editors Pages: 594 - 594
Association of Wilms tumour with spina bifida occulta P. KajtárJ. WeisenbachK. Méhes Letters to the Editors Pages: 594 - 595
A new therapeutic approach for X-linked adrenoleukodystrophy M. CappaE. BertiniG. Uziel Letters to the Editors Pages: 595 - 596
