Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Rht Edwards"'
Autor:
Malcolm J. Jackson, Rht Edwards
Publikováno v:
Acta Pharmacologica et Toxicologica. 59:136-138
Publikováno v:
Nephrology Dialysis Transplantation. 12:119-127
BACKGROUND Muscle weakness is a common but unexplained feature of dialysis patients. This study investigated the prevalence and causes of muscle weakness in dialysis patients by examining the quadriceps muscle force and contractile properties. METHOD
Publikováno v:
Neuromuscular Disorders. 5:171-178
Muscle imaging has been used largely as an adjunct in the assessment of patients with muscle disease and has been reported in descriptive terms only. Developments in computer-based image analysis techniques applied to muscle have enabled the quantifi
Publikováno v:
NMR in Biomedicine. 6:168-172
Fourteen patients with liver cirrhosis of differing severity participated in a one-dimensional chemical shift imaging 31P MRS study of the liver. Patients were divided into two groups according to the severity of their liver disease using Child's cla
Publikováno v:
International Journal of Sports Medicine. 13:S143-S146
Magnetic resonance spectroscopy (MRS) and imaging (MRI) are now well established techniques for the study of cellular metabolism and gross structure of muscle. Using non-ferrous materials, we have constructed a system for the measurement of isometric
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 262:E167-E172
We studied plasma ammonia and exercise tolerance in six patients with McArdle's disease (myophosphorylase deficiency, type V glycogenosis) during incremental cycle ergometry. Tests were performed either in the postabsorptive state or after supplement
Publikováno v:
QJM. 81:961-973
Publikováno v:
Clinica Chimica Acta. 203:119-134
Creatine kinase (CK) release in response to excessive electrically stimulated contractile activity has been studied in isolated rat soleus muscles. The exacerbation of CK release induced by contractile activity was found to be directly related to the
Publikováno v:
Biochemical Journal. 275:477-483
1. mdx mice do not express dystrophin, the product of the gene which is defective in Duchenne and Becker muscular dystrophy. We have previously shown that protein-synthetic rates (ks) are increased in mdx mouse muscles [MacLennan & Edwards (1990) Bio
Publikováno v:
Clinical Science. 80:367-371
1. Isolated extensor digitorum longus muscles from control C57BL/10 and mutant dystrophin-deficient C57BL/10 mdx mice have been studied in vitro to determine whether dystrophin deficiency influences the susceptibility of muscle to contractile activit