By Kat Duff
Release the stunning proof, myths, and advantages of 1 of the main endangered human resources—sleep.
It has develop into more and more transparent that our sleep shapes who we're up to, if no more than, we form it.
While so much sleep learn hasn’t ventured some distance past examine labs and remedy clinics, the key lifetime of Sleep faucets into the large reservoir of human studies to light up the complexities of a global the place sleep has turn into a dwindling source.
With a feeling of infectious interest, award profitable writer Kat Duff mixes state-of-the-art study with insightful narratives, surprising insights, and well timed inquiries to aid us greater comprehend what we’re wasting earlier than it’s too overdue.
The mystery lifetime of Sleep tackles the entire breadth of what sleep skill to humans across the world. Embark on an exploration of what lies in the back of and past our eyelids once we quit to the key lifetime of sleep.
Read Online or Download The Secret Life of Sleep PDF
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Additional info for The Secret Life of Sleep
Adenovirus-mediated gene transfer holds some promise in delivering a-glucosidase to muscle ( 418). The problems inherent in gene delivery to the brain are discussed by Kennedy ( 419). Allogeneic bone marrow transplantation offers more promise for the treatment of lysosomal storage diseases. In glycogenosis II, however, no beneficial result has been reported, despite successful engraftment. Liver transplantation has been used with some effect in type IV glycogen storage disease (brancher deficiency) ( 420).
Some have been of normal intelligence, or only mildly retarded, whereas others have presented with severe retardation and macrocephaly ( 468). Hepatomegaly is generally present, and the facial and skeletal abnormalities are characteristic for a mucopolysaccharidosis. 12) is readily detected in serum, leukocytes, and fibroblasts ( 469). Mucolipidoses Mucolipidoses have the clinical features of both the mucopolysaccharidoses and the lipidoses. At least four mucolipidoses have been distinguished, characterized by MPS storage despite normal excretion of MPS.
Corneal opacities are almost invariable, as is strabismus and an ERG with markedly reduced amplitude. Photophobia was noted in 25% of the children in the Israeli series of Amir and coworkers ( 475). A striking hypotonia and extrapyramidal signs also have been encountered, and some patients have been evaluated for a congenital myopathy. Seizures are not part of the clinical picture. Skeletal deformities and visceromegaly are absent (475). Curiously, patients with ML IV are constitutionally achlorhydric ( 476).