Increased high density lipoproteins in diabetic children U. EwaldS. GustafsonB. Vessby Original Investigations Pages: 154 - 156
Leukemic cell differentiation in childhood leukemias. Analysis by enzyme markers G. GaedickeH. G. Drexler Original Investigations Pages: 157 - 164
Steroid biochemistry of virilising adrenal tumours in childhood J. W. HonourD. A. PriceD. B. Grant Original Investigations Pages: 165 - 169
A developmental approach to the management of children with sleep disturbances in the first three years of life Remo H. LargoUrs A. Hunziker Original Investigations Pages: 170 - 173
Continuous ambulatory peritoneal dialysis in a program for children with end stage renal disease R. S. Fennell IIIJ. K. OrakM. I. Knight Original Investigations Pages: 174 - 178
Long-term follow-up of children with craniopharyngioma N. StahnkeG. GrubelR. P. Willig Original Investigations Pages: 179 - 185
Pseudopituitary dwarfism due to resistance to somatomedin: A new syndrome J. R. BierichH. MoellerR. G. Rosenfeld Original Investigations Pages: 186 - 188
Slight impairment of psychomotor skills in children after treatment of acute lymphoblastic leukemia G. HartenU. StephaniF. Hanefeld Original Investigations Pages: 189 - 197
Lung function in congenital and idiopathic scoliosis J. W. Owange-IrakaAilie HarrisonJ. O. Warner Original Investigations Pages: 198 - 200
Calcification of cartilages, brachytelephalangy and peripheral pulmonary stenosis. Confirmation of the Keutel syndrome J. P. FrynsA. van FleterenH. van den Berghe Original Investigations Pages: 201 - 203
Follow-up study of a nation-wide neonatal metabolic screening program in Japan K. TadaH. TatedaH. Naruse Original Investigations Pages: 204 - 207
Seven years of experience with selective screening for organic acidurias W. LehnertH. Niederhoff Original Investigations Pages: 208 - 210
Idiopathic infantile arterial calcification: a case report and review of the literature Ch. MaayanO. PelegJ. Bar Ziv Case Reports Pages: 211 - 215
Combined autoimmune neutro-and thrombocytopenia H. SchneiderA. JobkeW. Künzer Case Reports Pages: 216 - 219
Activity of renal 25-hydroxyvitamin D3-1α-hydroxylase in a case of X-linked hypophosphataemic rickets Y. SeinoK. SatomuraH. Yabuuchi Case Reports Pages: 219 - 222
Systemic carnitine deficiency: Benefit of oral carnitine supplements vs. persisting biochemical abnormalities M. DuranJ. B. C. de KlerkF. G. I. Jennekens Case Reports Pages: 224 - 228
Dysplastic features, growth retardation, malrotation of the gut, and fatal ventricular septal defect in a 4-month-old girl with ring chromosome 15 J. OttoE. BackW. Pringsheim Case Reports Pages: 229 - 231
Hereditary branchial arch defects in a Turkish family F. AksuH. B. v. StockhausenH.-J. Schultz-Coulon Letters to the Editor Pages: 232 - 233
The Tay syndrome (congenital ichthyosis with trichothiodystrophy) F. CrovatoC. BorroneGisela Bonsmann Letters to the Editor Pages: 233 - 234
Asthmatic attack associated with oral clonidine test S. AshkenaziM. MimouniI. Varsano Letters to the Editor Pages: 235 - 235