Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jacob Meer"'
Publikováno v:
Pediatric Neurology. 28:307-309
Hereditary neuropathy with liability to pressure palsies is an autosomal-dominant disorder, classically characterized by recurrent mononeuropathies, associated with a deletion at 17p11.2, encompassing the peripheral myelin protein 22 gene. The typica
Autor:
Robert N. Husson, Frank M. Balis, Philip A. Pizzo, Karina M. Butler, Sheila Judge Santacroce, Paul Jarosinski, Howard B. Moss, David G. Poplack, Jacob Meer, Mary E. Hawkins, Lori Wiener, Emile Brouwers, Michele Einloth, Janie Eddy, J. Falloon, Pam Wolters
Publikováno v:
The Journal of Pediatrics. 117:799-808
Objective: To determine whether a short course of 2′,3′-dideoxycytidine (ddC) could provide safe antiretroviral activity in children with symptomatic human immunodeficiency virus infection and whether it could be used with azidothymidine (AZT, zi
Autor:
Jim Dambrosia, Vitalie D. Lupu, Marinos C. Dalakas, Jacob Meer, Mary Kay Floeter, Carlos A. Mora
Publikováno v:
Musclenerve. 35(2)
Neuropathy with antibodies against myelin-associated glycoproteins (MAG/SGPG-N) and hereditary sensorimotor neuropathy type 1 (HMSN1) are characterized by chronic demyelination with little conduction block. Electrodiagnostic studies suggest that in H
Publikováno v:
Neurology. 41(10)
We measured sweat production to direct gland stimulation with intradermal methacholine in patients with autonomic failure and in normal subjects. The sympathetic skin response (SSR) to electrical stimulation was assessed in some of the same subjects.
Autor:
Paula D. Ravin, Marlene Mendiones, Roger A. Brumback, Martha B. Denckla, Ronald J. Polinsky, Sechin Cho, Mary B. Ganges, Lynn H. Gerber, Richard A. Guthrie, Jacob Meer, James R. Carl, Barbara C. Sonies, Jay H. Robbins, Susanna F. Barrett, Robert E. Tarone, Alan N. Moshell
Publikováno v:
Brain : a journal of neurology. 114
Xeroderma pigmentosum (XP) is an autosomal recessive, neurocutaneous disorder characterized by sunlight-induced skin cancers and defective DNA repair. Many XP children develop a primary neuronal degeneration. We describe 2 unusual XP patients who had
Autor:
Roger W. Gilliatt, Jacob Meer
Publikováno v:
Musclenerve. 13(5)
In patients with the carpal tunnel syndrome (CTS) and in control subjects, pairs of shocks at intervals of 0.8 msec and 1.0 msec were used to stimulate the median nerve just above the wrist. Nerve action potentials were recorded at the elbow and from
Autor:
R. V. La Rocca, Marinos C. Dalakas, Roger W. Gilliatt, Jacob Meer, Charles E. Myers, J. Cassidy, Cy A. Stein
Publikováno v:
Neurology. 40:954-954
We report the development of a severe polyneuropathy in 4 of 38 patients who were receiving parenteral suramin therapy for the treatment of various underlying malignancies. In 2 of these patients, the neuropathy progressed to generalized flaccid para
Publikováno v:
Muscle & Nerve. 11:848-851
We studied the rate of appearance and mechanism of contralateral R1 responses in normal subjects. Contralateral R1 could be produced by facilitating maneuvers such as a gentle contraction of the orbicularis oculi and conditioning stimulus of the medi
Autor:
Murray Solomon, Antonino Uncini, Dale J. Lange, Robert E. Lovelace, Betty Soliven, Jacob Meer
Publikováno v:
Musclenerve. 12(9)
Because digit 4 (D4) has dual innervation, median and ulnar sensory latencies can be determined over identical distances. To determine if D4 testing is more sensitive than other commonly used techniques to diagnose carpal tunnel syndrome (CTS), we ex