Zobrazeno 1 - 10
of 143
pro vyhledávání: '"G. Lopate"'
Autor:
W. Waheed, Alan Pestronk, G. Lopate, Muhammad Al-Lozi, J. Florence, I. Ramneantu, Todd Levine, M. Stambuk, Timothy M. Miller
Publikováno v:
Neurology. 62:461-464
Background: In the standard neurologic examination, outcome measures of sensation testing are typically qualitative and subjective. The authors compared the outcome of vibratory sense evaluation using a quantitative Rydel-Seiffer 64 Hz tuning fork wi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 73:420-428
Objectives: To study myopathies with serum antibodies to the signal recognition particle (SRP), an unusual, myositis specific antibody associated syndrome that has not been well characterised pathologically. Methods: Clinical, laboratory, and myopath
Autor:
C. Armon, V.P.M. Dal Bello-Haas, J.M. Florence, A.D. Kloos, J. Scheirbecker, G. Lopate, S.M. Hayes, E.P. Pioro, H. Mitsumoto
Publikováno v:
Neurology. 71:864-866
Publikováno v:
Muscle & Nerve. 21:1216-1219
N lines can be seen by electron microscopy within the I band of skeletal muscle, but are poorly visualized in conventional preparations. We present a case of acute quadriplegic myopathy with myosin loss and prominent N lines. The only other reported
Publikováno v:
Neurology. 59(9)
The authors report a patient with cervical dystonia, previously treated with botulinum toxin A (BTX-A), who developed bilateral ptosis and difficulty with accommodation only after botulinum toxin B (BTX-B). High-frequency repetitive nerve stimulation
Publikováno v:
Musclenerve. 21(9)
N lines can be seen by electron microscopy within the I band of skeletal muscle, but are poorly visualized in conventional preparations. We present a case of acute quadriplegic myopathy with myosin loss and prominent N lines. The only other reported
Publikováno v:
Journal of the neurological sciences. 151(2)
Anti-sulfatide antibodies are associated with polyneuropathies having a prominent sensory component, but with variable degrees of motor and sensory loss, gait dysfunction and demyelination. In this study, we asked whether patterns of IgM binding to n
Publikováno v:
Neurology. 48(4)
IgM anti-GM1 antibodies are associated with motor neuropathy syndromes, including multifocal motor neuropathy (MMN). We compared the ability of serum IgM from patients with multifocal motor neuropathy to bind to GM1 ganglioside alone and to GM1 as a
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