Benign partial epilepsy and related conditions: Multifactorial pathogenesis with hereditary impairment of brain maturation H. DooseW. K. Baier Review Pages: 152 - 158
Wilms tumour in a patient with growth hormone replacement therapy T. MomoiC. YamanakaH. Mikawa Endocrinology Pages: 159 - 161
Osteonecrosis of vertebrae in a child with acute lymphocytic leukaemia duringl-asparaginase therapy T. HanadaY. HorigomeH. Takita Hematology/Oncology Pages: 162 - 163
Serum IgG subclass concentrations in healthy subjects at different age: Age normal percentile charts A. PlebaniA. G. UgazioG. R. Burgio Immunology/Allergology Pages: 164 - 167
IgG2/IgG4 subclass deficiency in a patient with chronic mucocutaneous candidiasis and bronchiectases C. BräggerR. A. SegerW. H. Hitzig Immunology/Allergology Pages: 168 - 169
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes P. M. SchneiderC. WendlerC. Rittner Immunology/Allergology Pages: 170 - 174
Development of hypogammaglobulinaemia in a patient with common variable immunodeficiency A. IshizakaM. NakanishiS. Matsumoto Immunology/Allergology Pages: 175 - 176
Fatal infectious mononucleosis with staphylococcal pyoderma in a girl with hereditary immunological dysregulations T. InabaR. HanadaH. Hukada Immunology/Allergology Pages: 177 - 178
Facial dysmorphia, parathyroid and thymic dysfunction in the father of a newborn with the DiGeorge complex P. D. Maaswinkel-MooijS. E. PapapoulosJ. J. P. Van De Kamp Immunology/Allergology Pages: 179 - 183
Osteogenesis imperfecta in childhood: cardiac and renal manifestations U. VetterB. MaierhoferO. Wörsdörfer Medical Genetics Pages: 184 - 187
Keutel syndrome: A report of four cases H. E. KhosroshahiÖ. UluoğluC. Başaklar Medical Genetics Pages: 188 - 191
No reduction of high density lipoprotein2 during weight reduction in obese children and adolescents K. ZwiauerB. KerblK. Widhalm Metabolic Diseases Pages: 192 - 193
4-Hydroxybutyric aciduria: Further clinical heterogeneity in a new case W. OnkenhoutP. D. Maaswinkel-MooijB. J. H. M. Poorthuis Metabolic Diseases Pages: 194 - 196
The male disadvantage in very low birthweight infants: Does it really exist? S. P. Verloove-VanhorickD. M. van Zeben-van der AaJ. H. Ruys Neonatology Pages: 197 - 202
Frequent relapser minimal change nephrosis: An unrecognized X-linked disorder? N. B. AwadallaA. S. TeebiA. Shaltout Nephrology/Urology Pages: 205 - 207
Exogenous prostaglandin administration and pseudo-Bartter syndrome J. P. LanghendriesV. ThiryJ. M. Bertrand Nephrology/Urology Pages: 208 - 209
Symptomatology in children with focal sharp waves of genetic origin H. Doose Neuropediatrics Pages: 210 - 215
Role of protein C in childhood cerebrovascular occlusive accidents S. UysalB. AnlarS. Kirazli Neuropediatrics Pages: 216 - 218
Blood concentrations after accidental cyclosporin overdose K. de MeerR. H. J. HouwenM. J. H. Slooff Pharmacology Pages: 219 - 220
Sauna habits and related symptoms in Finnish children L. MarkkolaK. J. MattilaM. J. Koivikko Preventive Pediatrics and Epidemiology Pages: 221 - 222
