DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 04 · Volume 28 · August 1997 DOI: 10.1055/s-002-5734

Original articles

  • 191
    Schmitt, B.; Bauersfeld, U.; Fanconi, S.; Wohlrab, G.; Huisman, T. A. G. M.; Bandtlow, Ch.; Baumann, P.; Superti-Furga, A.; Martin, E.; Arbenz, U.; Molinari, L.; Turina, M.; Boltshauser, E.; Schmid, E. R.:

    The Effect of the N-methyl-D-aspartate Receptor Antagonist Dextromethorphan on Perioperative Brain Injury in Children Undergoing Cardiac Surgery with Cardiopulmonary Bypass: Results of a Pilot Study

  • 198
    Gropman, A. L.; Barkovich, A. J.; Vezina, L. G.; Conry, J. A.; Dubovsky, E. C.; Packer, R. J.:

    Pediatric Congenital Bilateral Perisylvian Syndrome: Clinical and MRI Features in 12 Patients

  • 204
    Steinlin, M.; Schmid, M.; Landau, K.; Boltshauser, E.:

    Follow-Up in Children with Joubert Syndrome

  • 212
    Topaloǧlu, H.; Dinçer, P.; Richard, I.; Akçören, Z.; Alehan, D.; Özme, Ş; Çaǧlar, M.; Karaduman, A.; Urtizberea, J. A.; Beckmann, J. S.:

    Calpain-3 Deficiency Causes a Mild Muscular Dystrophy in Childhood

  • 217
    Sewry, C. A.; D'Alessandro, M.; Wilson, L. A.; Sorokin, L. M.; Naom, I.; Bruno, S.; Ferlini, A.; Dubowitz, V.; Muntoni, F.:

    Expression of Laminin Chains in Skin in Merosin-Deficient Congenital Muscular Dystrophy

  • 223
    Vainzof, M.; Costa, C. S.; Marie, S. K.; Moreira, E. S.; Reed, U.; Passos-Bueno, M. R.; Beggs, A. H.; Zatz, M.:

    Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy

  • 229
    Sperl, W.; Felber, S.; Skladal, D.; Wermuth, B.:

    Metabolic Stroke in Carbamyl Phosphate Synthetase Deficiency

    • Short communication

  • 235
    Brandis, A.; Heyer, R.; Hori, A.; Walter, G. F.:

    Cerebellar Neurocytoma in an Infant: An Important Differential Diagnosis from Cerebellar Neuroblastoma and Medulloblastoma?

    • Letter to the editor

  • 239
    Weglage, J.; Bick, U.; Schuierer, G.; Pietsch, M.; Sprinz, A.; Zaß, R.; Ullrich, K.:

    Progression of Cerebral White Matter Abnormalities in Early Treated Patients with Phenylketonuria During Adolescence