Results 181 to 190 of about 20,100 (227)
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Current Paediatrics, 1997
Abstract Familial dysautonomia (FD, Riley-Day syndrome, hereditary sensory and autonomic neuropathy type III) can be considered a genetic model for understanding how perturbations in the autonomic nervous system and the sensory system can compromise cognition and alter behavior.
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Abstract Familial dysautonomia (FD, Riley-Day syndrome, hereditary sensory and autonomic neuropathy type III) can be considered a genetic model for understanding how perturbations in the autonomic nervous system and the sensory system can compromise cognition and alter behavior.
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Postganglionic cholinergic dysautonomia
Annals of Neurology, 1977AbstractA 9‐year‐old boy presented with symptoms and signs of marked postganglionic cholinergic autonomic dysfunction manifested by bilateral internal ophthalmoplegia, impaired secretion of tears and saliva, lack of gastrointestinal motility, atony of the bladder, generalized absence of sweating, and hypertension.
S I, Harik +3 more
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Sympathetic Cardioneuropathy in Dysautonomias
New England Journal of Medicine, 1997The classification of dysautonomias has been confusing, and the pathophysiology obscure. We examined sympathetic innervation of the heart in patients with acquired, idiopathic dysautonomias using thoracic positron-emission tomography and assessments of the entry rate of the sympathetic neurotransmitter norepinephrine into the cardiac venous drainage ...
D S, Goldstein +4 more
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Pediatrics, 1979
The study of 53 patients with dysautonomia by Welton et al (Pediatrics 63:708, 1979) is the most extensive survey of mental ability in this condition yet published. The conclusion is drawn "that the same proportion of the dysautonomic population scored within the average range of intelligence as if found in the general population." The ...
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The study of 53 patients with dysautonomia by Welton et al (Pediatrics 63:708, 1979) is the most extensive survey of mental ability in this condition yet published. The conclusion is drawn "that the same proportion of the dysautonomic population scored within the average range of intelligence as if found in the general population." The ...
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Nervenheilkunde, 2013
SummarySystemic amyloidosis is a life-threatening and frequently unrecognized cause of dysautonomia. Autonomic neuropathy is a common manifestation of AL amyloidosis (caused by deposition of an immunoglobulin free light chain produced by an underlying plasma cell clone) and of autosomal dominant hereditary ATTR amyloidosis (caused by a transthyretin ...
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SummarySystemic amyloidosis is a life-threatening and frequently unrecognized cause of dysautonomia. Autonomic neuropathy is a common manifestation of AL amyloidosis (caused by deposition of an immunoglobulin free light chain produced by an underlying plasma cell clone) and of autosomal dominant hereditary ATTR amyloidosis (caused by a transthyretin ...
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