Zobrazeno 1 - 10
of 52
pro vyhledávání: '"D, Horoupian"'
Autor:
Kara Weisiger, Seymour Packman, Nathan M. Bass, S. J. DeArmond, Charles L. Hoppel, D. Horoupian, Gregory M. Enns, Susan Schelley
Publikováno v:
Clinical Genetics. 68:337-348
Variation in the size and relative proportion of type 1 and type 2 muscle fibers can occur in a number of conditions, including structural myopathies, neuropathies, and various syndromes. In most cases, the pathogenesis of such fiber type changes is
Autor:
C. F. Lippa, J. P. Vonsattel, D. Horoupian, Koichi Wakabayashi, Dennis W. Dickson, P. L. Lantos, Massimo Tabaton, K. Ikeda, C. Bergeron, C. Duyckaerts, S. S. Mirra, Irene Litvan, S. S. Chin, K. Jellinger
Publikováno v:
Scopus-Elsevier
A working group supported by the Office of Rare Diseases of the National Institutes of Health formulated neuropathologic criteria for corticobasal degeneration (CBD) that were subsequently validated by an independent group of neuropathologists. The c
Autor:
G M, Enns, C L, Hoppel, S J, DeArmond, S, Schelley, N, Bass, K, Weisiger, D, Horoupian, S, Packman
Publikováno v:
Clinical genetics. 68(4)
Variation in the size and relative proportion of type 1 and type 2 muscle fibers can occur in a number of conditions, including structural myopathies, neuropathies, and various syndromes. In most cases, the pathogenesis of such fiber type changes is
Autor:
D, Horoupian
Publikováno v:
Pediatric pathologylaboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association. 15(1)
Publikováno v:
Neurology. 31:464-467
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 40:73-79
A patient with clinical features of idiopathic normal pressure hydrocephalus, who responded dramatically to shunting, was found a necropsy to have a severe hypertensive and arteriosclerotic vasculopathy with multiple lacunar infarcts. There was no pa
Autor:
P, Pick, D, Horoupian
Publikováno v:
Clinical neuropathology. 3(2)
A 53-year-old chronic alcoholic male developed an acute febrile, fulminant fatal encephalopathy which lasted 2.5 weeks. Necropsy showed focal, acute hemorrhagic necrotizing lesions of the diencephalon, cingulate gyrus, and amygdala, apparently due to
Publikováno v:
Neurology. 33(8)
A 51-year-old woman who had systemic Weber-Christian disease (WCD) displayed multiple xanthomatous lesions and a large xanthogranuloma of the tentorium cerebelli with signs of brainstem and cerebellar compression. Three other cases of dural xanthomat
Autor:
C S, Raine, D, Horoupian
Publikováno v:
Musclenerve. 3(2)
Publikováno v:
Transactions of the American Neurological Association. 103