DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 19 · November 1988 DOI: 10.1055/s-002-10719

Original articles

  • 171
    Angelini, L.; Rumi, V.; Lamperti, E.; Nardocci, N.:

    Transient Paroxysmal Dystonia in Infancy

  • 175
    Korinthenberg, R.; Ullrich, K.; Füllenkemper, F.:

    Evoked Potentials and Electroencephalography in Adolescents with Phenylketonuria

  • 179
    Roodhooft, A. M.; Van Acker, K. J.; Van Thienen, M. N.; Martin, J. J.; Ceuterick, C.:

    Marshall-Smith Syndrome: New Aspects

  • 183
    van de Bor, Margot; Verloove-Vanhorick, S. Pauline; Baerts, W.; Brand, R.; Ruys, J. H.:

    Outcome of Periventricular-Intraventricular Hemorrhage at 2 Years of Age in 484 Very Preterm Infants Admitted to 6 Neonatal Intensive Care Units in The Netherlands* **

  • 186
    Illum, N.; Reske-Nielsen, Edith; Skovby, F.; Askjær, S. A.; Bernsen, Alice:

    Lethal Autosomal Recessive Arthrogryposis Multiplex Congenita with Whistling Face and Calcifications of the Nervous System

  • 193
    Kálmánchey, R.; Veres, E.:

    Dancing Eyes Syndrome - Brainstem Acoustic Evoked Potential Approach

  • 197
    Barth, P. G.; Stam, F. C.; Hack, W.; Delemarre-van de Waal, H. A.:

    Gliomatosis Cerebri in a Newborn

  • 201
    Andre, M.; Matisse, N.; Vert, P.; Debruille, Ch.:

    Neonatal Seizures - Recent Aspects

    • Case report

  • 208
    Bošnjak, V.; Bešenski, N.; Marušić Della-Marina, B.; Polak, J.:

    Ultrasonography in Hereditary Degenerative Diseases of the Cerebral White Matter in Infancy

  • 212
    Linssen, W. H. J. P.; Fiselier, T. J. W.; Gabreëls, F. J. M.; Wevers, R. A.; Cuppen, M. P. M. J.; Rotteveel, J. J.:

    Acute Transverse Myelopathy as the Initial Manifestation of Probable Systemic Lupus Erythematosus in a Child

  • 216
    van der Wal, A. C.; Troost, D.:

    Enterogenous Cyst of the Brainstem - A Case Report

  • 218
    Boel, M.; Casaer, P.:

    Familial Periodic Ataxia Responsive to Flunarizine

  • 221
    Novotny Jr , E. J.:

    Arthrogryposis Associated with Connatal Pelizaeus-Merzbacher Disease: Case Report