Zobrazeno 1 - 10 of 27 pro vyhledávání: '"R L Schelper"'
1
Partial protection from salt-induced stroke and mortality by high oral calcium in hypertensive rats
Autor: J D Peuler, R L Schelper
Publikováno v: Stroke. 23:532-538
Repeated demonstration of an antihypertensive effect of high oral calcium in stroke-prone spontaneously hypertensive rats led us to determine whether it also protects such rats from premature mortality and stroke-related lesions. Female stroke-prone
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ee3dc4852e6c0454263f8d8e2c7784
https://doi.org/10.1161/01.str.23.4.532
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2
The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ('pallido-ponto-nigral degeneration')
Autor: R. L. Schelper, L. A. Reed, Brian J. Balin, John Q. Trojanowski, Zbigniew K. Wszolek, Marie L. Schmidt, Virginia M.-Y. Lee, Virawudh Soontornniyomkij
Publikováno v: Journal of neuropathology and experimental neurology. 57(6)
A group of similar autosomal dominant hereditary neurodegenerative disorders have been linked to chromosome 17 in thirteen kindreds. One of these disorders, known as pallido-ponto-nigral degeneration (PPND), is characterized by extensive degeneration
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af8cd7c14a192445ca4ab1839ee77f17
https://pubmed.ncbi.nlm.nih.gov/9630238
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3
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q
Autor: K D, Mathews, K A, Mills, H L, Bailey, R L, Schelper, J C, Murray
Publikováno v: Musclenerve. Supplement. 2
Myodystrophy (myd) is an autosomal-recessive mouse mutation with dystrophic skeletal muscle. We propose that myd may be a model of the human disorder facioscapulohumeral dystrophy (FSHD) on the basis of clinical features and homologous genetic map lo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0cd7ff2709cf8df3eb86e2c37106e149
https://pubmed.ncbi.nlm.nih.gov/7739634
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6
beta-amyloid protein of Alzheimer's disease is found in cerebral and spinal cord vascular malformations
Autor: M N, Hart, P, Merz, J, Bennett-Gray, A H, Menezes, J A, Goeken, R L, Schelper, H M, Wisniewski
Publikováno v: The American journal of pathology. 132(1)
Congo/Red deposition with birefringence to polarized light was demonstrated focally in cerebrovascular malformations removed surgically from 4 older patients (ages 85, 74, 74, and 63), and in a spinal cord vascular malformation in a 76-year-old patie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::aae59547a1d9cdfee25d76439a44aa56
https://pubmed.ncbi.nlm.nih.gov/3293463
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8
Brain microvascular smooth muscle expresses class II antigens
Autor: M N, Hart, M M, Waldschmidt, J M, Hanley-Hyde, S A, Moore, J D, Kemp, R L, Schelper
Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 138(9)
Mouse (BALB/c) splenic lymphocytes co-cultured in vitro with syngeneic brain-derived microvascular smooth muscle (SM) proliferate and become activated. After subsequent transfer of the activated lymphocytes to a syngeneic host, a vasculitis develops
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::44e4e449a48209dbcd831595bb5073fc
https://pubmed.ncbi.nlm.nih.gov/3471815
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10
Ependymal cyst of the subarachnoid space. Cytologic diagnosis and developmental considerations
Autor: R L, Schelper, I, Ramzy, N, Durr
Publikováno v: Acta cytologica. 29(1)
Fluid aspirated from a subarachnoid cystic lesion that covered and compressed part of the left frontal lobe was examined cytologically and compared with histologic sections of the cyst wall. The fluid contained epithelial and histiocytelike cell popu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7efb3d4e21d3ad41c7cb373e9a964a5f
https://pubmed.ncbi.nlm.nih.gov/3855586
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