By Aertsen A., Braitenberg V. (eds.)
The current choice of papers makes a speciality of the topic of imaginative and prescient. The papers compile new insights and proof from quite a few branches of experimental and theoretical neuroscience. The experimental proof awarded within the quantity stem from disparate fields, resembling neuroanatomy, electrophysiology, optical imaging and psychophysics. The theoretical types partially are unsophisticated, but nonetheless inspiring, whereas others skilfully practice complicated mathematical reasoning to result of experimental measurements. The e-book is the 5th in a sequence of volumes aspiring to outline a thought of the mind by way of bringing jointly formal reasoning and experimental evidence. The reader is hence being brought to a brand new form of mind technology, the place evidence and idea are commencing to mix jointly.
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G. g. g. of size [micropsia, macropsia], shape, position) Loss or dulling of vision (amaurosis) Eyelid ﬂuttering, blinking, nystagmus The clinical forms and causes of epilepsy reported. Sexual feelings can occur sometimes with erection or ejaculation. Gustatory seizures have their origin in the suprasylvian region (adjacent to the mouth and throat primary sensory region). Ictal vertigo also originates in the suprasylvian region. Transient postictal sensory deﬁcits or spatial disorientation occur.
85. Childhood absence epilepsy Childhood absence epilepsy (pyknolepsy) appears in the early and middle years of childhood (peak age 6–7 years), more commonly in girls than in boys and usually in children without learning disability or other neurological problems. It accounts for between 1 and 3% of newly diagnosed epilepsies and up to 10% of childhood epilepsies. The absence seizures (see p. 7) usually last 10–15 seconds, and are so brief that in many cases they pass unrecognized for long periods.
Almost all cases are associated with coeliac disease, which may be demonstrable only on jejunal biopsy. Other rarer but interesting childhood benign focal syndromes have been described, sometimes in a handful of families only, and include: benign partial epilepsy in infancy, idiopathic photosensitive occipital lobe epilepsy, idiopathic frontal lobe epilepsy, familial temporal lobe epilepsy, autosomal dominant rolandic epilepsy with speech dyspraxia, and benign focal seizures in adolescents. 17).