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Myelin
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Myelin : The Brain's Supercharger

Book Details

Format Hardback or Cased Book
ISBN-10 019068609X
ISBN-13 9780190686093
Publisher Oxford University Press Inc
Imprint Oxford University Press Inc
Country of Manufacture US
Country of Publication GB
Publication Date Oct 25th, 2018
Print length 328 Pages
Weight 504 grams
Dimensions 14.60 x 21.60 x 2.40 cms
Ksh 8,000.00
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Emerging 425 million years ago during our evolution, the substance known now as myelin enables the split-second acceleration of nerve impulses. Remarkably, myelin occupies nearly half the volume of the human brain and is critical for our intellectual and motor performance. We owe our reflexes to myelin: it is what makes us brake when a child dashes out onto the road, or snatch away a hand absent-mindedly placed on a burning hot stove.The study of myelin''s role in the conduction of nerve impulses has led to a better understanding of several diseases including multiple sclerosis, Guillain-Barre syndrome, Charcot-Marie-Tooth peripheral neuropathies, and other genetic diseases of myelin.
The emergence of myelin 425 million years ago marked a turning point in evolution. Consider for a moment the invention of insulated wire, which allows for the transmission of electrical current. Functioning in a similar way, the membrane surrounding nerve fibers, or myelin, enables the remarkable acceleration of nerve impulses. Surprisingly, myelin occupies nearly half the volume of the human brain and is critical for our intellectual and motor performance. Without myelin, our thoughts and our movements would suffer overwhelming delays. We owe our reflexes to myelin: it is what makes us brake when a child dashes out onto the road, or snatch away a hand absent-mindedly placed on a burning hot stove. When damaged, myelin can lead to irreversible disability, cognitive decline, and sensory impairments. The study of myelin''s role in the conduction of nerve impulses has led to a better understanding of several diseases including multiple sclerosis, Guillain-Barre syndrome, Charcot-Marie-Tooth peripheral neuropathies, and other genetic diseases of myelin.

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