Persistent microalbuminuria in adolescents with Type I (insulin-dependent) diabetes mellitus is associated to early rather than late puberty M. JannerS. Eberhard KnillP. E. Mullis Endocrinology Pages: 403 - 408
Painfulness of needle and jet injection in children with diabetes mellitus U. SchneiderR. BirnbacherE. Schober Endocrinology Pages: 409 - 410
Virilizing adrenal tumour mimicking congenital adrenal hyperplasia with P450c11 (11β-hydroxylase) deficiency E. A. WerderR. VoutilainenM. Zachmann Endocrinology Pages: 411 - 415
Monitoring steatorrhoea in cystic fibrosis M. De CurtisF. SantamariaF. Ciccimarra Gastroenterology/Hepatology Pages: 416 - 418
A clinical trial with an “anti-regurgitation” formula Yvan VandenplasSaid Hachimi-IdrissiHelmuth Loeb Gastroenterology/Hepatology Pages: 419 - 423
Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease) Emmanuel JacqueminMicheline DumontMichelle Hadchouel Gastroenterology/Hepatology Pages: 424 - 428
Focal fatty liver change in a 12-year-old Japanese boy M. IgarashiY. AkiyamaY. Nakashima Gastroenterology/Hepatology Pages: 429 - 431
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease V. SchusterS. SeidenspinnerH. W. Kreth Immunology/Allergology Pages: 432 - 437
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients C. Schrander-StumpelP. MeineckeJ. P. Fryns Medical Genetics Pages: 438 - 445
Branchio-Oto-Renal (BOR) syndrome: variable expressivity in a five-generation pedigree R. KönigS. FuchsC. Dukiet Medical Genetics Pages: 446 - 450
Normal growth and normalization of hypergonadotropic hypogonadism in atypical Turner syndrome (45,X/46,XX/47,XXX) C. -J. PartschR. PankauMarlis Tolksdorf Medical Genetics Pages: 451 - 455
Neonatal portal vein thrombosis successfully treated by regional streptokinase infusion V. K. RehanC. M. G. CroninJ. M. Bowman Neonatology Pages: 456 - 459
Familial isolated pulmonary hypoplasia: a case report, suggesting autosomal recessive inheritance B. FreyA. FleischhauerM. Gersbach Pneumology Pages: 460 - 463
Methylmalonic acidaemia: haplotype analysis of the methylmalonyl-CoA-mutase gene in Europe C. BenderA. BüchlerF. K. Trefz Letters to the Editors Pages: 468 - 468
A possible relationship between polyarteritis nodosa and hydatid disease A. BakkaloğluO. SöylemezoğluÜ. Saatci Letters to the Editors Pages: 469 - 469
Pubertal development in thalassaemic patients after allogenic bone marrow transplantation V. De SanctisM. GalimbertiC. Vullo Erratum Pages: 470 - 470
