Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D. L. Murman"'
Autor:
B. Bayer, D. L. Murman, D. Bessette, Diego Torres-Russotto, Rebecca Thompson, Danish Bhatti, Mark Harry Fleisher, Nabeel Muzaffar Syed, Kalyan Malgireddy
Publikováno v:
Clinical Parkinsonism & Related Disorders
Clinical Parkinsonism & Related Disorders, Vol 1, Iss, Pp 10-12 (2019)
Clinical Parkinsonism & Related Disorders, Vol 1, Iss, Pp 10-12 (2019)
Background Orthostatic Tremor (OT) is a rare movement disorder characterized by a sensation of unsteadiness while standing and associated with high frequency tremors. Patients with OT commonly report a fear of falling and significant limitations in e
Autor:
Diego Torres-Russotto, E. Piccione, S. Kedar, J.A. Fernandes, John M. Bertoni, O. Taraschenko, D. L. Murman, P. Fayad, Rebecca Thompson, Danish Bhatti, R. High, James Shou
Publikováno v:
Parkinsonism & Related Disorders. 46:e27
Autor:
D. L. Murman, A. M. Mellow, Roderick J. A. Little, Jewel R. Johanns, Norman L. Foster, Bruno Giordani, M. Hariharan
Publikováno v:
Neurology. 49:153-161
Background: Excitotoxicity may contribute to neuronal degeneration in Huntington's disease (HD). N-methyl-D-aspartate (NMDA) receptor antagonists can prevent neuronal degeneration caused by excitotoxicity, but their effects in HD patients are not kno
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 7:251-255
Apolipoprotein E (apoE) Ε4 allele frequency among Alzheimer''s disease (AD) patients is increased compared to control subjects and is influenced by the presence of other genetic factors and age at symptom onset. We examined the relationship between
Autor:
James T. Warren, D. L. Murman, Allen D. Roses, John K. Fink, Anders A. F. Sima, Michael L. Peacock
Publikováno v:
Annals of Neurology. 35:432-438
Amyloid plaques in Alzheimer's disease contain beta-amyloid, encoded by portions of exons 16 and 17 of the amyloid precursor protein. The specific association of rare amyloid precursor protein mutations with some kindreds with early-onset familial Al
Publikováno v:
European Journal of Neurology. 14:e5-e6
Publikováno v:
Neurology. 41(10)
We analyzed the prion protein coding sequence in a familial Creutzfeldt-Jakob disease patient who did not have any of the currently recognized prion protein mutations. Denaturing gradient gel electrophoresis indicated that the prion protein coding se
Autor:
D. L. Murman, R. D. McComb
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 48:357