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Average vertical velocity (in pascals per second) at the 500 hPa pressure height in July from 1979–2001. Ascent (negative values) is concentrated close to the solar equator while descent (positive values) is more diffuse; their distribution is an imprint of the ascending and descending branches of the Hadley circulation.
Severe acute respiratory syndrome coronavirus 2: bats, felines, raccoon dogs, minks, white-tailed deer [4] respiratory transmission 2019–present COVID-19 pandemic; ongoing pandemic. Cowpox: Cowpox virus: rodents, cattle, cats direct contact with infected animals Creutzfeldt-Jacob disease: PrP vCJD: cattle
Ascent (negative values; blue to violet) is concentrated close to the solar equator; descent (positive values; red to yellow) is more diffuse but also occurs mainly in the Hadley cell. The wind belts girdling the planet are organised into three cells in each hemisphere—the Hadley cell, the Ferrel cell, and the polar cell. Those cells exist in ...
L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS).
A clinically isolated syndrome (CIS) is a clinical situation of an individual's first neurological episode, caused by inflammation or demyelination of nerve tissue. An episode may be monofocal , in which symptoms present at a single site in the central nervous system , or multifocal , in which multiple sites exhibit symptoms.
The diseases are not restricted to Finns; they are genetic diseases with far wider distribution in the world, but due to founder effects and genetic isolation they are more common in Finns. Within Finland these diseases are more common in the east and north, consistent with their higher association with ethnic Finns than with ethnic Swedes . [ 2 ]
Humoral immune deficiencies are conditions which cause impairment of humoral immunity, which can lead to immunodeficiency.It can be mediated by insufficient number or function of B cells, the plasma cells they differentiate into, or the antibody secreted by the plasma cells. [7]
Diagnosis of DRPLA rests on positive family history, clinical findings, and genetic testing. Family history can be difficult to obtain if a relative was misdiagnosed, died young, or experiences late onset of symptoms. [citation needed] Other diseases in the differential diagnosis of adult-onset DRPLA include Huntington's and the spinocerebellar ...