DOI: 10.1055/s-00000041

Neuropediatrics

Issue 06 · Volume 26 · December 1995 DOI: 10.1055/s-002-6626

  • 287
    Voit, T.:

    Editorial

    • Original articles

  • 288
    Rocchigiani, M.; Sestini, S.; Micheli, V.; Pescaglini, M.; Jacomelli, G.; Hayek, G.; Pompucci, G.:

    Purine and Pyridine Nucleotide Metabolism in the Erythrocytes of Patients with Rett Syndrome

  • 293
    Vainzof, M.; Marie, S. K. N.; Reed, U. C.; Schwartzman, J. S.; Pavanello, R. C. M.; Passos-Bueno, M. R.; Zatz, M.:

    Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter Alterations

  • 298
    Shawkat, Fatima S.; Kingsley, D.; Kendall, B.; Russell-Eggitt, Isabelle; Taylor, D. S. I.; Harris, Chr. M.:

    Neuroradiological and Eye Movement Correlates in Children with Intermittent Saccade Failure: "Ocular Motor Apraxia"

    • Short communications

  • 306
    Derex, L.; Isnard, H.; Revol, M.:

    Progressive Facial Hemiatrophy with Multiple Benign Tumors and Hamartomas

  • 310
    Brandt, B. Ryde; Rosén, I.:

    Impaired Peripheral Somatosensory Function in Children with Down Syndrome

  • 313
    Gascon, G. G.; Chavis, P.; Yaghmour, A.; Stigsby, B.; Ozand, P.; Siddique, T.:

    Familial Childhood Primary Lateral Sclerosis with Associated Gaze Paresis

  • 320
    Boltshauser, E.; Forster, I.; Deonna, T.; Willi, U.:

    Joubert Syndrome: Are Kidneys Involved?

  • 322
    Barbot, C.; Martins, E.; Vilarinho, L.; Dorche, C.; Cardoso, M. L.:

    A Mild Form of Infantile Isolated Sulphite Oxidase Deficiency

  • 325
    Gordon, B. A.; Gordon, K. E.; Seo, H. C.; Yang, M.; DiCioccio, R. A.; O'Brien, J. S.:

    Fucosidosis with Dystonia

  • 328
    Zammarchi, E.; Donati, M. A.; Ciani, F.:

    Transient Neonatal Nonketotic Hyperglycinemia: A 13-Year Follow-Up

  • 331
    Boltshauser, E.; Gehrmann, J.; Steinlin, M.; Eich, G.; Spiegel, R.:

    Progressive Subcutaneous and Periarticular Calcifications in a Patient with Spinal Muscular Atrophy Type III

    • Letters to the editor

  • 333
    Rees, M.; Elmslie, F.; Whitehouse, W.; Sundqvist, A.; Gardiner, M.:

    Analysis of a Human Brain Voltage-Gated Potassium Channel Gene, KCNA6 (HBK2), in Patients with Juvenile Myoclonic Epilepsy

  • 335
    Anlar, B.; Kuruoǧlu, R.; Varh, K.; Renda, Y.:

    Acetylcholine Receptor Antihodies and Single-Fiber EMG in First-Degree Relatives of Children with Myasthenia Gravis