3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients K. M. GibsonJ. BreuerW. L. Nyhan Review Pages: 180 - 186
Right ventricular performance and pulmonary haemodynamics in adolescent and adult patients with cystic fibrosis O. C. BurghuberU. Salzer-MuharM. Götz Cardiology Pages: 187 - 192
Cardiomyopathy associated with carnitine loss in kidneys and small intestine R. Rodrigues PereiraH. R. ScholteM. H. M. Vaandrager-Verduin Cardiology Pages: 193 - 197
Arteriovenous haemangioma of the joint capsule of the knee in a child D. GozalM. SoudryJ. H. Boss Cardiology Pages: 198 - 199
The effect of gonadotrophin releasing hormone analogue on height prognosis in growth hormone deficiency and normal puberty R. StanhopeC. G. D. Brook Endocrinology Pages: 200 - 202
Carditis complicating inflammatory bowel disease in children E. GranotM. RottemA. J. J. T. Rein Gastroenterology/Hepatology Pages: 203 - 205
Sonography of subependymal cysts in congenital rubella syndrome C. BeltingerH. Saule Imaging Techniques Pages: 206 - 207
Acute rheumatic fever in the young: changing prevalence and pattern G. EshelJ. BarrG. Mundel Immunology/Allergology Pages: 208 - 210
Undetectable IgG4 in immunoprecipitation: association with repeated infections in children? P. BartmannE. Kleihauer Immunology/Allergology Pages: 211 - 214
Immunoglobulin deficiency with increased immunoglobulin M in three siblings: effect of long-term immunoglobulin therapy L. MaródiI. SzabóÁ. Kalmár Immunology/Allergology Pages: 215 - 217
Intravenous gammaglobulin in treatment of isoimmune neonatal neutropenia T. HanadaR. ShinH. Takita Immunology/Allergology Pages: 218 - 219
Noonan syndrome: growth and clinical manifestations in 144 cases M. B. RankeP. HeidemannJ. R. Bierich Medical Genetics Pages: 220 - 227
Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency T. MatsumotoT. KondohN. Niikawa Medical Genetics Pages: 228 - 232
Reduced insulin removal and erythrocyte insulin binding in obese children M. KnipP. LautalaR. Puukka Metabolic Diseases Pages: 233 - 237
Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine C. LykkelundJ. B. NielsenF. Güttler Metabolic Diseases Pages: 238 - 245
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency W. EndresY. S. ShinS. K. Wadman Metabolic Diseases Pages: 246 - 249
Mevalonate kinase deficiency in a child with cerebellar ataxia, hypotonia and mevalonic aciduria K. M. GibsonG. HoffmannG. P. A. Smit Metabolic Diseases Pages: 250 - 252
Sympatho-adrenal response to hypoglycaemia in infants B. StanekA. LischkaA. Pollak Neonatology Pages: 253 - 256
Postnatal course of plasma levels of adrenocortical steroids in premature infants with and without NaCl supplementation E. SulyokH. G. DörrGy. Gyódi Neonatology Pages: 257 - 261
Oral versus intramuscular loading of caffeine in idiopathic apnoea of prematurity L. CattarossiV. ColacinoF. Macagno Neonatology Pages: 262 - 263
Transient hyperphosphatasaemia of infancy E. SchönauK. H. HerzogH. J. Böhles Neonatology Pages: 264 - 266
Hyperamino-acidaemia and hyperammonaemia in epileptic children treated with valproic acid K. IinumaK. HayasakaK. Hori Neuropediatrics Pages: 267 - 269
Angelman (“happy puppet”) syndrome —seven new cases documented by cerebral computed tomography: review of the literature A. DörriesH. -L. SpohrJ. Kunze Neuropediatrics Pages: 270 - 273
Preliminary data on a field study with a new hypo-allergic formula Y. VandenplasM. DeneyerH. Loeb Nutrition Pages: 274 - 277
Theophylline pharmacokinetics in children, comparing sustained release spheres (Theo-Dur sprinkle) with elixir N. -I. M. KjellmanS. CronerS. -O. Thuresson Pharmacology Pages: 278 - 280
