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pro vyhledávání: '"J. M. Evanson"'
Enhanced cell proliferation, glycolysis and prostaglandin E production are all characteristic features of rheumatoid synovial tissue. The interrelationships of these three cellular parameters have been examined using rheumatoid synovial fibroblasts a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d6f7a0642f3bc8e3dc4504f0e56d7e
https://ora.ox.ac.uk/objects/uuid:044fc7a4-216a-4cee-b856-28d6d6c0db1f
https://ora.ox.ac.uk/objects/uuid:044fc7a4-216a-4cee-b856-28d6d6c0db1f
Publikováno v:
Rheumatology International. 11:37-40
The presence of circulating IgG, IgA and IgM antibodies to native cartilage collagens in some patients with rheumatoid arthritis (RA) suggests that an autoimmune response to cartilage collagens may be involved in the pathogenesis of RA. However, the
Publikováno v:
Journal of psychosomatic research. 45(5)
This article describes a prospective, randomized, controlled trial of screening and treatment for psychiatric disorder in medical in-patients. The study has assessed whether increased recognition of psychiatric disorder among medical in-patients impr
Publikováno v:
Circulatory shock. 37(2)
Interleukin-1 alpha (IL-1 alpha) produced alterations in human dermal fibroblast glucose metabolism in vitro of the type seen in severe sepsis in man. Glycolysis and glucose uptake were increased but the oxidation of glucose within the tricarboxylic
Publikováno v:
British journal of hospital medicine. 43(1)
Autor:
F. B. Beswick, J. M. Evanson
Publikováno v:
The Journal of Physiology. 135:400-411
Publikováno v:
New England Journal of Medicine. 271:283-287
IDIOPATHIC paroxysmal myoglobinuria, variously described as paroxysmal paralytic myoglobinuria, idiopathic recurrent rhabdomyolysis with myoglobinuria and spontaneous myoglobinuria, is a rare disorder of voluntary muscle characterized by episodes of
Autor:
F. B. Beswick, J. M. Evanson
Publikováno v:
The Journal of Physiology. 128:89-98
Autor:
J M Evanson, B E Juel-Jensen
Publikováno v:
Postgraduate Medical Journal. 49:375-379
Publikováno v:
BMJ. 2:485-487
Seventeen patients with Paget's disease of the skull and deafness were followed for nine to 18 months. Patients who received calcitonin treatment showed less deterioration in hearing than untreated patients. Calcitonin treatment may retard the progre