DOI: 10.1055/s-00000041

Neuropädiatrie

Issue 01 · Volume 8 · February 1977 DOI: 10.1055/s-002-13159

Original article

  • 3
    Gerken, H.; Kiefer, R.; Doose, H.; Völzke, E.:

    Genetic Factors in Childhood Epilepsy with Focal Sharp Waves1– I. Clinical Data and Familial Morbidity for Seizures

  • 10
    Doose, H.; Gerken, H.; Kiefer, R.; Völzke, E.:

    Genetic Factors in Childhood Epilepsy with Focal Sharp Waves1– II. EEG Findings in Patients and Siblings

  • 21
    Dietrich, K.; Gaab, M.; Knoblich, O. E.; Schupp, J.; Ott, B.:

    A New Miniaturized System for Monitoring the Epidural Pressure in Children and Adults

  • 29
    Windorfer, A.; Sauer, W.:

    Drug Interactions During Anticonvulsant Therapy in Childhood: Diphenylhydantoin, Primidone, Phenobarbitone, Clonazepam, Nitrazepam, Carbamazepin and Dipropylacetate

    • Case report

  • 42
    Lenard, H. G.; Goebel, H. H.; Weigel, W.:

    Smooth Muscle Involvement in Congenital Myotonic Dystrophy

  • 53
    Kyllerman, M.:

    Infantile Spinal Muscular Atrophy (Morbus Werdnig-Hoffmann) Causing Neonatal Asphyxia

  • 57
    Boltshauser, E.; Isler, W.:

    Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar Vermis

  • 67
    Holmgren, G.; Blomquist, H. K:son:

    Non-Ketotic Hyperglycinemia in Two Sibs with Mild Psycho-Neurological Symptoms

  • 73
    Vuia, O.:

    Congenital Spongy Degeneration of the Brain (Van Bogaert – Bertrand) Associated with Micrencephaly and Ponto – Cerebellar Atrophy (Contributions to the Pathology of Glial Dystrophy of Intrauterin Origin)

  • 89
    Verity, M. A.; Montasir, M.:

    Infantile Gaucher's Disease: Neuropathology, Acid Hydrolase Activities and Negative Staining Observations1