Results 251 to 260 of about 1,837,376 (291)

Neurological Manifestations of Aging

Journal of Gerontology, 1977
A group of 51 socially active, self-declared neurologically normal subjects ranging from 61 to 84 years of age were studied with a battery of clinical neurological examinations and a semiquantitative vibration perception test. None of the subjects showed a consistent pattern of neurological deficit that could be identified as pathological. On review of
E, Kokmen, R W, Bossemeyer, J, Barney, W J, Williams   +3 more
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Neurologic Manifestations of Sarcoidosis

Neurologic Clinics, 2002
Sarcoidosis is multisystem granulomatous disease of unknown etiology. Although the nervous system is involved in only 5% to 16% of patients, neurosarcoidosis is one of the more serious manifestations of the disease. Cranial neuropathies are common, but involvement of the mininges or the brain or spinal cord parenchyma causes more severe morbidity.
Dakshinamurty, Gullapalli, Lawrence H, Phillips   +1 more
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Neurological Manifestations in COVID-19 Patients: A Meta-Analysis

ACS Chemical Neuroscience, 2021
Common symptoms such as dizziness, headache, olfactory dysfunction, nausea, vomiting, etc. in COVID-19 patients have indicated the involvement of the nervous system.
Vitalakumar D, A. Sharma, Anoop Kumar, S. Flora   +3 more
semanticscholar   +1 more source

Neurological Manifestations in Otolaryngology

Archives of Otolaryngology - Head and Neck Surgery, 1961
To appreciate the protean manifestations of neurologic, and the frequently related emotional, disorders affecting the head and neck areas, is to realize the morphological complexity of the human mechanism and its susceptibility to a wide range of disturbing experiences.
F L, LEDERER, E M, SKOLNIK
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Uveitis with Neurological Manifestations

International Ophthalmology Clinics, 2001
Neurological symptoms are not rare in patients with various uveitic syndromes, and they can be used as a guide to diagnosis. Some of the findings are nonspecific, but others can be typical of certain pathological conditions (table). After combining the information obtained in the medical history with the physical examination, target-oriented laboratory
V L, Perez, C S, Foster
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Encephalocraniocutaneous Lipomatosis: Neurologic Manifestations

Journal of Child Neurology, 2003
We report a new case of encephalocraniocutaneous lipomatosis, a rare neurocutaneous syndrome of unknown etiology with involvement of tissues arising from the mesoderm and ectoderm: skin, eye, adipose tissue, and brain. We also review the neurologic manifestations of the syndrome, the most frequent of which include seizures, ventricular enlargement ...
Rafael, Lasierra, Ignacio, Valencia, Francisco J, Carapeto, Purificación, Ventura, M Pilar, Samper, Gerardo, Rodríguez, José M, Pérez-González, Agustín, Legido   +7 more
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Neurologic manifestations of homocystinuria

Clinical Neurology and Neurosurgery, 1981
Recognition of the disease homocystinuria by the neurologist may be of importance as is illustrated in the dramatic case history of a 20 year old woman. Confusion with Marfan's syndrome frequently occurs. The clinical and pathologic anatomical features are described. A review of the literature is given and the use of contraceptives is discussed.
H C, Schoonderwaldt, G H, Boers, J R, Cruysberg, B P, Schulte, J L, Slooff, H O, Thijssen   +5 more
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Neurological manifestations of gnathostomiasis

Journal of the Neurological Sciences, 1977
Neurological features of 24 patients with nervous system gnathostomiasis were reviewed. The commonest presenting features were radiculomyelitis or radiculomyelitis terminating with encephalitis, and subarachnoid haemorrhage. A primary encephalitic form was noted in 2 patients.
P, Boongird, P, Phuapradit, N, Siridej, T, Chirachariyavej, S, Chuahirun, A, Vejjajiva   +5 more
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Neurologic manifestations of achondroplasia

2014
Achondroplasia is the best described and most common form of the congenital short-limbed dwarfing conditions. Achondroplasia is apparent at birth and has a birth prevalence of 1 in 20000-30000 live-born infants. Achondroplasia is inherited as an autosomal dominant condition, although 80% of cases occur sporadically as new events in their families ...
Jacqueline T, Hecht, John B, Bodensteiner, Ian J, Butler   +2 more
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Neurologic Manifestations of Myxedema

New England Journal of Medicine, 1962
Headache Headache, a vague, subjective symptom, often encountered, but difficult to evaluate, seems to occur quite frequently in the myxedematous patient although the underlying mechanism is not clear. The headache is usually described as chronic, recurrent, bilateral and diffuse, and quite unlike sinusitis, migraine, eyestrain and the incidental ...
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