نتایج جستجو برای: urbach wiethe disease
تعداد نتایج: 1490423 فیلتر نتایج به سال:
SIEBENMANN (1908) described lipidproteinosis, and the condition was subsequently reported as a clinical entity by Urbach and Wiethe (1929). During infancy and early childhood a structureless eosinophilic substance develops under the epithelium of the skin and upper respiratory tract. Hoarseness is followed by a skin eruption giving a pale, yellow-brown, pock-marked appearance, especially on the...
Numerous neuroimaging studies have strongly implicated the amygdala in dreaming. Various neuropsychological dream theories propose roles for the amygdala in dreaming (particularly in the generation of dream affect), however little empirical research on its function in dreaming exists. Urbach Wiethe Disease is a very rare genetic condition which leads to calcification of the amygdala over time. ...
A Jewish-Iranian family suffered from lipoid proteinosis. The 8 affected siblings were from consanguineous matings and presented a wide range of phenotypic expressions. Minimal manifestations in 2 heterozygote carriers and the possibility of autosomal recessive inheritance are discussed.
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