DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 21 · November 1990 DOI: 10.1055/s-002-12372

A special article

  • 171
    Menkes, J. H.; Kinsbourne, M.:

    Workshop on Neurologic Complications of Pertussis and Pertussis Vaccination

    • Original article

  • 177
    Robinson, R. O.:

    Arthrogryposis Multiplex Congenita; Feeding, Language and Other Health Problems

  • 179
    Cusmai, R.; Curatolo, P.; Mangano, S.; Cheminal, R.; Echenne, B.:

    Hemimegalencephaly and Neurofibromatosis

  • 183
    Tanaka, J.; Mimaki, T.; Okada, Sh.; Fujimura, H.:

    Changes in Cerebral White Matter in a Case of Congenital Muscular Dystrophy (Non-Fukuyama Type)

  • 187
    Murakami, K.; Sugimoto, T.; Nishida, N.; Woo, M.; Araki, A.; Kobayashi, Y.; Sakane, Y.:

    Carnitine Metabolism and Morphometric Change of Liver Mitochondria in Valproate-Treated Rats

  • 191
    Barišić, Nina; Škarpa, D.; Jušić, A.; Jadro-Šantel, D.:

    Steroid Responsive Familial Neuropathy with Liability to Pressure Palsies

  • 193
    Hashimoto, T.; Tayama, M.; Miyazaki, M.; Kuroda, Y.; Hiura, K.; Hujino, K.; Yamashita, K.:

    Cranial MR Imaging in Patients with von Recklinghausen's Disease (Neurofibromatosis Type I)

  • 199
    Kyllerman, M.; Blomstrand, S.; Månsson, J.-E.; Conradi, N. G.; Hindmarsh, T.:

    Central Nervous System Malformations and White Matter Changes in Pseudo-Neonatal Adrenoleukodystrophy*

  • 202
    Bennett, M. J.; Galloway, J. H.; Cartwright, I. J.; Gillis, W. S.; Hosking, G. P.:

    Decreased Erythrocyte and Platelet Phospholipids and Fatty Acids in Juvenile Neuronal Ceroid-Lipofuscinosis (Batten Disease)

  • 206
    Moodley, M.; Moosa, A.:

    Chondrodystrophic Myotonia (Schwartz-Jampel Syndrome) in South African Children

    • Case report

  • 211
    McShane, M. A.; Finn, J. P.; Hall-Craggs, M. A.; Hanmer, O.; Harper, J.:

    Neonatal Hemangiomatosis Presenting as Infantile Spasms

  • 213
    Deonna, Th.; Roulet, E.; Meyer, H. U.:

    Benign Paroxysmal Tonic Upgaze of Childhood - A New Syndrome*

  • 215
    Haddad, J.; Messer, J.; Gut, J. P.; Chaigne, D.; Christmann, D.; Willard, D.:

    Neonatal Echovirus Encephalitis with White Matter Necrosis

  • 218
    Harbord, M. G.; Boyd, S.; Hall-Craggs, M. A.; Kendall, B.; McShane, M. A.; Baraitser, M.:

    Ataxia, Developmental Delay and an Extensive Neuronal Migration Abnormality in 2 Siblings

  • 222
    Vigevano, F.; Di Rocco, C.:

    Effectiveness of Hemispherectomy in Hemimegalencephaly with Intractable Seizures

    • Letter to the editor

  • 224
    Parano, E.:

    Walker-Warburg Syndrome