DOI: 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 30 · February 1999 DOI: 10.1055/s-002-5713

Invited review

  • 1
    de Koning, T. J.; Poll-The, B. T.; Jaeken, J.:

    Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders

    • Rapid publication

  • 5
    Mayatepek, E.; Lindner, M.; Zelezny, R.; Lindner, W.; Brandstetter, G.; Hoffmann, G. F.:

    A Severely Affected Infant with Absence of Cysteinyl Leukotrienes in Cerebrospinal Fluid: Further Evidence that Leukotriene C4-Synthesis Deficiency is a New Neurometabolic Disorder

    • Original articles

  • 8
    Mercuri, E.; Jongmans, Marian; Bouza, Helen; Haataja, Leena; Rutherford, Mary; Henderson, Sheila; Dubowitz, Lilly:

    Congenital Hemiplegia in Children at School Age: Assessment of Hand Function in the Non-Hemiplegic Hand and Correlation with MRI

  • 14
    Iai, M.; Takashima, S.:

    Thalamocortical Development of Parvalbumin Neurons in Normal and Periventricular Leukomalacia Brains

  • 19
    Goutières, Françoise; Dollfus, Hélène; Becquet, F.; Dufier, J.-L.:

    Extensive Brain Calcification in Two Children with Bilateral Coats' Disease

  • 22
    Mahjneh, I.; Bushby, K.; Anderson, L.; Muntoni, F.; Tolvanen-Mahjneh, H.; Bashir, R.; Pizzi, A.; Brockington, M.; Marconi, G.:

    Merosin-Positive Congenital Muscular Dystrophy: A Large Inbred Family

  • 29
    Urlesberger, B.; Kaspirek, A.; Pichler, C.; Müller, W.:

    Apnoea of Prematurity and Changes in Cerebral Oxygenation and Cerebral Blood Volume

  • 34
    Oka, Akira; Itoh, M.; Takashima, S.:

    The Early Induction of Cyclooxygenase 2 Associated with Neurofibrillary Degeneration in Brains of Patients with Fukuyama-Type Congenital Muscular Dystrophy

    • Short communications

  • 38
    Østergaard, J. R.; Christensen, T.; Nehen, Anne Marie:

    A Distinct Difference in Clinical Expression of Two Siblings with Aicardi-Goutières Syndrome

  • 42
    de Lonlay-Debeney, P.; Edery, P.; Cormier-Daire, Valerie; Parfait, Béatrice; Chrétien, Dominique; Rötig, Agnès; Romero, Norma; Saudubray, J.-M.; Munnich, A.; Rustin, P.:

    Respiratory Chain Deficiency Presenting as Recurrent Myoglobinuria in Childhood

  • 45
    Incorpora, G.; Di Gregorio, F.; Romeo, M. A.; Pavone, P.; Trifiletti, R. R.; Parano, E.:

    Focal Neurological Deficits in Children with β-Thalassemia Major

    • Letters to the editor

  • 49
    Anlar, B.; Ozdirim, E.:

    Thymectomy in Children with Myasthenia Gravis

  • 50
    Weglage, J.; Pietsch, M.; Sprinz, A.; Feldmann, R.; Denecke, J.; Kurlemann, G.:

    A Previously Unpublished Side Effect of Sulthiame in a Patient with Rolandic Epilepsy

  • 51
    Hauser, S. E. P.; Boneh, A.:

    Severe Clinical Course with Recurrent Hyperpyrexia in a Patient with Glutaric Aciduria Type I