DOI: 10.1055/s-00000041

Neuropädiatrie

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

Original article

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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
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Doose, H.; Gerken, H.; Kiefer, R.; Völzke, E.: Genetic Factors in Childhood Epilepsy with Focal Sharp Waves1– II. EEG Findings in Patients and Siblings
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Dietrich, K.; Gaab, M.; Knoblich, O. E.; Schupp, J.; Ott, B.: A New Miniaturized System for Monitoring the Epidural Pressure in Children and Adults
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Windorfer, A.; Sauer, W.: Drug Interactions During Anticonvulsant Therapy in Childhood: Diphenylhydantoin, Primidone, Phenobarbitone, Clonazepam, Nitrazepam, Carbamazepin and Dipropylacetate

Case report

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Lenard, H. G.; Goebel, H. H.; Weigel, W.: Smooth Muscle Involvement in Congenital Myotonic Dystrophy
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Kyllerman, M.: Infantile Spinal Muscular Atrophy (Morbus Werdnig-Hoffmann) Causing Neonatal Asphyxia
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Boltshauser, E.; Isler, W.: Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar Vermis
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Holmgren, G.; Blomquist, H. K:son: Non-Ketotic Hyperglycinemia in Two Sibs with Mild Psycho-Neurological Symptoms
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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)
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Verity, M. A.; Montasir, M.: Infantile Gaucher's Disease: Neuropathology, Acid Hydrolase Activities and Negative Staining Observations1