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A typical radiation pattern of phased arrays whose inter-element spacing is greater than half a wavelength, hence the radiation pattern has grating lobes.. For discrete aperture antennas (such as phased arrays) in which the element spacing is greater than a half wavelength, a spatial aliasing effect allows plane waves incident to the array from visible angles other than the desired direction ...
It is typically diffuse, involving larger areas of one or multiple lobes. There are a variety of potential causes, including Pneumocystis pneumonia, late-stage adenocarcinoma, pulmonary edema, some types of idiopathic interstitial pneumonias, diffuse alveolar hemorrhage, sarcoidosis, and pulmonary alveolar proteinosis. [ 6 ]
For discrete aperture antennas (such as phased arrays) in which the element spacing is greater than a half wavelength, the spatial aliasing effect causes some sidelobes to become substantially larger in amplitude, and approaching the level of the main lobe; these are called grating lobes, and they are either identical, or nearly identical as shown in the figure, copies of the main beams.
Gerstmann syndrome is a neurological disorder that is characterized by a constellation of symptoms [1] that suggests the presence of a lesion usually near the junction of the temporal and parietal lobes at or near the angular gyrus. Gerstmann syndrome is typically associated with damage to the inferior parietal lobule of the dominant hemisphere ...
Impaired blood flow to the cells of the occipital lobe (ischemia, for example as caused by a TIA or Vertebrobasilar insufficiency) will lead to temporary visual problems; if the poor blood flow is sustained it will lead to cell death (infarction, for example as caused by a stroke) which may cause persistent visual problems.
Typical treatment for pneumonitis includes conservative use of corticosteroids such as a short course of oral prednisone or methylprednisolone. Inhaled corticosteroids such as fluticasone or budesonide may also be effective for reducing inflammation and preventing re-inflammation on a chronic level by suppressing inflammatory processes that may ...
Pelger–Huët anomaly is a blood laminopathy associated with the lamin B receptor, [2] wherein several types of white blood cells (neutrophils and eosinophils) have nuclei with unusual shape (being bilobed, peanut or dumbbell-shaped instead of the normal trilobed shape) and unusual structure (coarse and lumpy).
Frontotemporal lobar degeneration; Neuropathologic analysis of brain tissue from FTLD-TDP patients. Ubiquitin immunohistochemistry in cases of familial FTLD-TDP demonstrates staining of (a) neurites and neuronal cytoplasmic inclusions in the superficial cerebral neocortex, (b) neuronal cytoplasmic inclusions in hippocampal dentate granule cells, and (c) neuronal intranuclear inclusions in the ...