DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 03 · Volume 21 · August 1990 DOI: 10.1055/s-002-12371

Original article

115
Deliac, Ph.; Demarquez, J. L.; Barberot, J. P.; Sandler, B.; Paty, J.: Brainstem Auditory Evoked Potentials in Icteric Fullterm Newborns: Alterations After Exchange Transfusion
119
Tanaka, K.; Nishizawa, K.; Yamamoto, H.; Naruto, T.; Izeki, E.; Taga, T.; Shimada, M.; Saeki, Y.: Analysis of Very Long-Chain Fatty Acids and Plasmalogen in the Erythrocyte Membrane: A Simple Method for the Detection of Peroxisomal Disorders and Discrimination Between Adrenoleukodystrophy and Zellweger Syndrome
124
Belec, L.; Tayot, J.; Tron, P.; Mikol, J.; Scaravilli, F.; Gray, F.: Cytomegalovirus Encephalopathy in an Infant with Congenital Acquired Immuno-Deficiency Syndrome
130
Amato, M.; Hüppi, P.; Durig, P.; Kaiser, G.; Schneider, H.: Fetal Ventriculomegaly Due to Isolated Brain Malformations
133
de Grauw, T. J.; Smit, L. M. E.; Brockstedt, M.; Meijer, Y.; v d Klei-v Moorsel, J.; Jakobs, C.: Acute Hemiparesis as the Presenting Sign in a Heterozygote for Ornithine Transcarbamylase Deficiency
136
De Vries, L. S.; Pierrat, V.; Minami, T.; Smet, M.; Casaer, P.: The Role of Short Latency Somatosensory Evoked Responses in Infants with Rapidly Progressive Ventricular Dilatation*
140
Yalaz, K.; Topçu, M.; Topaloğlu, H.; Gürçay, Ö; Özcan, O. E.; Önol, B.; Renda, Y.: N-Acetylaspartic Aciduria in Canavan Disease: Another Proof in Two Infants
143
Gaggero, R.; Cornaglia Ferraris, P.; De Negri, M.: CSF Anomalies in Children Affected by Epilepsia Partialis Continua (EPC)
146
Sperner, J.; Schmauser, I.; Bittner, R.; Henkes, H.; Bassir, C.; Sprung, C.; Scheffner, D.; Felix, R.: MR-Imaging Findings in Children with Sturge-Weber Syndrome
153
Forsgren, L.; Sidenvall, R.; Blomquist, H. K.; Heijbel, J.; Nyström, L.: An Incident Case-Referent Study of Febrile Convulsions in Children: Genetical and Social Aspects

Case report

160
Baraitser, Paula; Shieff, Colin: Cutaneomeningo-Spinal Angiomatosis: The Syndrome of Cobb. A Case Report
162
Kapusta, L.; Daniëls, O.; Renier, W. O.: Moya-Moya Syndrome and Primary Pulmonary Hypertension in Childhood
164
Harbord, M. G.; Harden, A.; Harding, B.; Brett, E. M.; Baraitser, M.: Megalencephaly with Dysmyelination, Spasticity, Ataxia, Seizures and Distinctive Neurophysiological Findings in Two Siblings