Neuropädiatrie
Issue 01 · February 1977
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Original article
3
Gerken, H.; Kiefer, R.; Doose, H.; Völzke, E.:
Genetic Factors in Childhood Epilepsy with Focal Sharp Waves
1
– I. Clinical Data and Familial Morbidity for Seizures
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10
Doose, H.; Gerken, H.; Kiefer, R.; Völzke, E.:
Genetic Factors in Childhood Epilepsy with Focal Sharp Waves
1
– II. EEG Findings in Patients and Siblings
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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
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29
Windorfer, A.; Sauer, W.:
Drug Interactions During Anticonvulsant Therapy in Childhood: Diphenylhydantoin, Primidone, Phenobarbitone, Clonazepam, Nitrazepam, Carbamazepin and Dipropylacetate
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Case report
42
Lenard, H. G.; Goebel, H. H.; Weigel, W.:
Smooth Muscle Involvement in Congenital Myotonic Dystrophy
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53
Kyllerman, M.:
Infantile Spinal Muscular Atrophy (Morbus Werdnig-Hoffmann) Causing Neonatal Asphyxia
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57
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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67
Holmgren, G.; Blomquist, H. K:son:
Non-Ketotic Hyperglycinemia in Two Sibs with Mild Psycho-Neurological Symptoms
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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)
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89
Verity, M. A.; Montasir, M.:
Infantile Gaucher's Disease: Neuropathology, Acid Hydrolase Activities and Negative Staining Observations
1
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