Zobrazeno 1 - 10
of 38
pro vyhledávání: '"J. E. Parisi"'
Publikováno v:
Neuropathology and applied neurobiology. 38(2)
Rapid eye movement sleep behaviour disorder (RBD) is characterized by loss of muscle atonia during rapid eye movement sleep and is associated with dream enactment behaviour. RBD is often associated with α-synuclein pathology, and we examined if ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b6dfd6c9f634664a905c2368d746bc6
https://pubmed.ncbi.nlm.nih.gov/21696423
https://pubmed.ncbi.nlm.nih.gov/21696423
Publikováno v:
European journal of neurology. 17(7)
Frontotemporal lobar degeneration (FTLD) can be subdivided into those in which the abnormal protein is tau (FTLD-TAU), the TAR DNA binding protein 43 (FTLD-TDP) and the fused in sarcoma protein (FTLD-FUS). We have observed severe caudate atrophy at a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d2a73604ab710fdef72dee4dbd56341
https://pubmed.ncbi.nlm.nih.gov/20236174
https://pubmed.ncbi.nlm.nih.gov/20236174
Publikováno v:
Annals of neurology. 47(3)
CADASIL, an autosomal dominant arteriopathy responsible for stroke and dementia, is caused by strongly stereotyped mutations in the Notch3 gene. We report a patient with a condition strongly suggestive of CADASIL (migraine, stroke, and white matter a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87d4a40c6e5389500326b60459e79485
https://pubmed.ncbi.nlm.nih.gov/10716263
https://pubmed.ncbi.nlm.nih.gov/10716263
Publikováno v:
Annals of neurology. 45(4)
We report on a 28-year-old man with long-standing intractable complex partial and secondary generalized seizures, whose magnetic resonance imaging scans 4 years apart documented progressive decrease in the left hippocampal volume. Left anterior tempo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f974db1bd191c0916e08efaf270357f4
https://pubmed.ncbi.nlm.nih.gov/10211480
https://pubmed.ncbi.nlm.nih.gov/10211480
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 14(2)
Prehension is an ideationally simple, cued movement requiring proximal (transport) and distal (manipulation) limb control. Patients with this syndrome of progressive apraxia are unable to perform many activities of daily living that require prehensio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9b7c1454f09b7c56599455fc843c683
https://pubmed.ncbi.nlm.nih.gov/10091622
https://pubmed.ncbi.nlm.nih.gov/10091622
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 13(3)
We report a rare case of Erdheim-Chester disease (ECD) presenting as a progressive cerebellar syndrome and diabetes insipidus. On magnetic resonance imaging, a 7-mm extraaxial, enhancing mass was seen enveloping the right vertebral artery and was con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::881e1188698c6c680554f8677d1d8a59
https://pubmed.ncbi.nlm.nih.gov/9613758
https://pubmed.ncbi.nlm.nih.gov/9613758
Autor:
R E, McLendon, R C, Bentley, J E, Parisi, R D, Tien, J C, Harrison, N J, Tarbell, A L, Billitt, R J, Gualtieri, H S, Friedman
Publikováno v:
Archives of pathologylaboratory medicine. 121(5)
Malignant neoplasms exhibiting mixed populations of neuronal and glial cells occurring in the cerebral hemispheres of young adults and children are well recognized, but rare. A confusing array of diagnostic terms has arisen. We describe two patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25864307c557e4869428694e63f70130
https://pubmed.ncbi.nlm.nih.gov/9167602
https://pubmed.ncbi.nlm.nih.gov/9167602
Autor:
T, Gómez-Isla, R, Hollister, H, West, S, Mui, J H, Growdon, R C, Petersen, J E, Parisi, B T, Hyman
Publikováno v:
Annals of neurology. 41(1)
To assess the relationship between dementia, neuronal loss, and neuropathological findings in Alzheimer's disease (AD), we counted the number of neurons, senile plaques, and neurofibrillary tangles in a high-order association cortex. We studied the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea90a1a24229026ef52a322b0cd6ab35
https://pubmed.ncbi.nlm.nih.gov/9005861
https://pubmed.ncbi.nlm.nih.gov/9005861
Publikováno v:
Journal of neurosurgery. 85(3)
Recent studies have suggested that a deficiency of alpha 1-antitrypsin may be a genetic risk factor for the development of intracranial aneurysms and arterial fibromuscular dysplasia. The authors report a 16-year-old girl with a history of lung disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b1c8ac16dacf491936379f4138d0d14c
https://pubmed.ncbi.nlm.nih.gov/8751640
https://pubmed.ncbi.nlm.nih.gov/8751640
Publikováno v:
Clinical chemistry. 41(2)
The concentrations of five essential elements and six potentially toxic elements were determined in seven organs collected at autopsy from 30 human subjects. Elemental analyses were carried out by graphite furnace atomic absorption spectroscopy, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3bae1636b8164212f0599f714c9fd81c
https://pubmed.ncbi.nlm.nih.gov/7874782
https://pubmed.ncbi.nlm.nih.gov/7874782