Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Lowell L. Williams"'
Publikováno v:
Archives of Physical Medicine and Rehabilitation. 75:787-791
In Charcot-Marie-Tooth syndrome (CMT, Hereditary Motor Sensory Neuropathy), patient complaints of cold intolerance are common but their peripheral responses to cold have not been documented. Using digital plethysmography, a simple test of vascular re
Autor:
Francis S. Wright, Lowell L. Williams
Publikováno v:
Journal of the Neurological Sciences. 120:195-200
Altered proportions of long-chain unsaturated n - 6 fatty acids (FA) in plasma and myelin of the heredodegenerative peripheral neuropathy, Charcot-Marie-Tooth syndrome (CMT), may implicate FA metabolism in the pathogenesis of CMT demyelination. A sig
Publikováno v:
Journal of Clinical Immunology. 13:389-396
Activated T cells, measured repeatedly in the demyelinating peripheral neuropathy, Charcot-Marie-Tooth syndrome (CMT; hereditary motor sensory neuropathy), might participate in myelin loss by a destructive inflammatory autoimmune process. To explore
Autor:
Louis J. Lafrado, Mark G. Lewis, Lloyd A. Horrocks, Lowell L. Williams, Jennifer L. Rojko, Richard G. Olsen
Publikováno v:
Experimental Biology and Medicine. 202:239-245
The polyunsaturated omega-6 fatty acid, arachidonic acid ([AA] 20:4n-6), is both the key of the immunoregulatory substances, prostaglandins, and leukotrienes, and an essential component of immune cell membrane phospholipids, providing stability and f
Publikováno v:
American Journal of Medical Genetics. 45:92-96
Charcot-Marie-Tooth disease type 1A (CMT1A) was recently demonstrated to be associated with a large DNA duplication in 17p11.2p12. The gene for neurofibromatosis type 1 (NF1) or von Recklinghausen disease maps to 17q11.2. We have identified 2 unrelat
Autor:
Ronald Glaser, Joel Hillhouse, Janice K. Kiecolt-Glaser, Lloyd A. Horrocks, Lowell L. Williams
Publikováno v:
Prostaglandins, Leukotrienes and Essential Fatty Acids. 47:165-170
Medical students (MS) tested during the first year of medical school showed both greater stress on the Brief Symptom Inventory and lower plasma proportions of total esterified arachidonic acid (AA, C20:4n-6), and its omega-6 fatty acid (FA) precursor
Autor:
Robert B. Chambers, Barry T. Shannon, Frederick H. Davidorf, Lowell L. Williams, Lawrence E. Leguire
Publikováno v:
Clinical Immunology and Immunopathology. 64:78-83
Systemic immunostimulation followed an experimental treatment trial of scatter argon laser photocoagulation directed to the retina of one eye of 10 patients with heredo-degenerative retinitis pigmentosa (RP). Significantly increased RP lymphocyte CD2
Publikováno v:
Journal of Neuroimmunology. 36:147-155
To evaluate possible immune-mediated mechanisms in hereditary motor and sensory neuropathy (HMSN-I, Charcot-Marie-Tooth syndrome), we examined class II major histocompatibility complex antigen expression (MHC-II, HLA-DR) in Schwann cells and peripher
Autor:
Pedro Mancias, Richard K. Olney, Cornelius F. Boerkoel, Karen M. Krajewski, Shelley J. Kennedy, Carlos A. Garcia, Lowell L. Williams, Hiroshi Takashima, Paul Russo, James R. Lupski, Ian J. Butler, Mena Scavina, Michael E. Shy, Katherine Berry, John L. Johnson, Ahmad S. Teebi
Publikováno v:
Annals of neurology. 51(2)
Charcot-Marie-Tooth disease (CMT) is a genetically heterogeneous disorder that has been associated with alterations of several proteins: peripheral myelin protein 22, myelin protein zero, connexin 32, early growth response factor 2, periaxin, myotubu
Publikováno v:
Journal of Infectious Diseases. 166:528-530
Elevated serum ELISA IgG antibodies to rubella virus (RV) were found by three independent determinations in 41 (72%) of 57 adults with the retinal degeneration retinitis pigmentosa, while antibody responses to five other common neurotropic viruses we