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Current drug therapy--antiepilepsy agents.
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[Psychopathological syndromes in epilepsy].
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Anesthesiologic considerations in psychiatric convulsive therapy.
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Clinical evaluation of Morfolep.
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[Epilepsies in the adult. Can we distinguish progressive types?].
Electro-clinical, neuro-radiologic and socio-professional study of 100 epileptic adults, followed by the same physician during 12 to 20 years (average 15 1/2 years), now 30 to 75 years old, all cases of evolutive pathology being excluded. The evolution statistically is more favourable when the epilepsy: has developed late (between 21 and 30 years); ils described as "idiopathic", or with small primary lesion; is characterized by primary generalized fits with strong convulsive component, occurring preferably at awaking. The evolution is less favourable, even unfavourable, when the epilepsy: is secondary to a severe encephalopathy or to extensive focal lesions; has developed during childhood; is characterized by fits with partial start, little tendency to secondary convulsive generalization, and occurring any time of the day or bound to sleep.
[Familial progressive myoclonus epilepsy (pme) (type Unverricht)].
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[The necessity of comparative morphology in epilepsy].
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Neurological disease in an English city.
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[Studies on the ammonia content in the serum of children with brain damage with special reference to hyperammonemia].
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Ultraviolet-absorbing urinary components. II. Mentally retarded children and abnormal rats.
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Development of so-called "genuine" epileptic seizures in dogs during emotional excitement.
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[Outpatient therapy of epilepsy].
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[The modern treatment of various forms of epileptic attacks and other symptoms of epileptic illnesses].
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[Contribution to the problem of hormone treatment in children with nodding spasms].
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[Moadon in the management of child seizures].
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[The West-syndrome and its treatment with ACTH].
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[Early results (initial effects) of the treatment with mogadan in propulsive petit mal epilepsy].
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