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Charles Miller Fisher (December 5, 1913, Waterloo, Ontario – April 14, 2012, Albany, New York) was a Canadian neurologist whose notable contributions include the first detailed descriptions of lacunar strokes, the identification of transient ischemic attacks as stroke precursors, the identification of the link between carotid atherosclerosis and stroke, and the description of a variant form ...
Other symptoms can include numbness in the face, arm, or leg, particularly if it’s one side of the body, confusion, trouble seeing, trouble walking, and a severe headache with no known cause.
Symptoms of a DVT will include unilateral leg swelling and pain, warmth, and redness of the affected area. [9] This is due to the blockage of blood attempting to return to the heart through the venous system. Additional findings in a patient with a paradoxical embolism will be dependent upon where the emboli lodges and disrupts blood flow.
Elsevier's parent company, RELX, has a global workforce that is 51% female to 49% male, with 43% female and 57% male managers, and 29% female and 71% male senior operational managers. [38] [39] In 2018, Elsevier accounted for 34% of the revenues of RELX group (£2.538 billion of £7.492 billion).
Sacco’s collaborative research advanced the understanding of stroke and cardiovascular and brain health, and helped elucidate the impact of modifiable behaviors, such as alcohol consumption and ...
The founder of Guild, the $4.4 billion education and upskilling startup, had just driven her twin girls home from their last day of preschool; they were next door at their father’s house for the ...
The following is a list of notable deaths in October 1999.. Entries for each day are listed alphabetically by surname. A typical entry lists information in the following sequence:
CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the NOTCH3 gene on chromosome 19. [1] The disease belongs to a family of disorders called the leukodystrophies.