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共有 10420 条符合本次的查询结果, 用时 3.6751524 秒

8841. Causes of mortality in systemic sclerosis.

作者: M Ho.;J Belch.
来源: Rheumatology (Oxford). 1999年38卷3期283-4页

8842. Adult Still's disease with nephrotic syndrome at presentation.

作者: A Jassim.;N Kumar.;C Kelly.
来源: Rheumatology (Oxford). 1999年38卷3期283页

8843. Granisetron (Kytril) suppresses methotrexate-induced nausea and vomiting among patients with inflammatory arthritis and is superior to prochlorperazine (Stemetil).

作者: J Devlin.;K Wagstaff.;V Arthur.;P Emery.
来源: Rheumatology (Oxford). 1999年38卷3期280-2页
Methotrexate (MTX) is an increasingly popular anti-rheumatic drug with its usefulness limited by toxicity, most commonly gastrointestinal (GI). The aim of the study was to study the effectiveness of the 5-HT3 receptor antagonist granisetron (GR) in the therapy of MTX-induced nausea.

8844. The prevalence and associated features of chronic widespread pain in the community using the 'Manchester' definition of chronic widespread pain.

作者: I M Hunt.;A J Silman.;S Benjamin.;J McBeth.;G J Macfarlane.
来源: Rheumatology (Oxford). 1999年38卷3期275-9页
We examine the descriptive epidemiology of chronic widespread pain using the 'Manchester' definition [CWP(M)] and assess psychosocial and other features which characterize subjects with such pain according to these more stringent criteria.

8845. Forces measured during spinal manipulative procedures in two age groups.

作者: M C Harms.;S M Innes.;D L Bader.
来源: Rheumatology (Oxford). 1999年38卷3期267-74页
Manipulation techniques have a prominent, yet controversial, role in the treatment of back pain. Their use varies widely between the professional groups and between individual therapists, with no accurate method of standardizing or quantifying the treatment administered.

8846. The detection of DNA from a range of bacterial species in the joints of patients with a variety of arthritides using a nested, broad-range polymerase chain reaction.

作者: N Z Wilkinson.;G H Kingsley.;H W Jones.;J Sieper.;J Braun.;M E Ward.
来源: Rheumatology (Oxford). 1999年38卷3期260-6页
Bacteria have been implicated in the pathogenesis of many types of inflammatory arthritides. The aim of this study was to identify any bacterial DNA in synovial fluid (SF) from patients with a range of inflammatory arthritides.

8847. Cyclosporin A therapy in rheumatoid arthritis: only strict application of the guidelines for safe use can prevent irreversible renal function loss.

作者: B E van den Borne.;R B Landewé.;H S Goei The.;F C Breedveld.;B A Dijkmans.
来源: Rheumatology (Oxford). 1999年38卷3期254-9页
To investigate (1) whether the increase in serum creatinine observed during cyclosporin A (CsA) therapy was reversible in a group of patients with rheumatoid arthritis (RA) treated before the current guidelines for safe use in RA were developed and (2) whether the application of these guidelines prevents serum creatinine increases in the long term.

8848. Primary Sjögren's syndrome in the North East of England: a long-term follow-up study.

作者: B K Davidson.;C A Kelly.;I D Griffiths.
来源: Rheumatology (Oxford). 1999年38卷3期245-53页
Although primary Sjogren's syndrome is often a benign condition, characterized by lymphocytic infiltration of salivary and lacrimal glands, some patients develop systemic features. We have previously found that anti-Ro antibodies identified patients with more systemic disease, with increased incidence of parotid swelling, lymphadenopathy and lymphoma.

8849. Ankylosing spondylitis: what is the optimum duration of a clinical study? A one year versus a 6 weeks non-steroidal anti-inflammatory drug trial.

作者: M Dougados.;A Gueguen.;J P Nakache.;P Velicitat.;E M Veys.;H Zeidler.;A Calin.
来源: Rheumatology (Oxford). 1999年38卷3期235-44页
To consider the relevance of the duration of a clinical trial in ankylosing spondylitis: long-term (i.e. 1 yr) vs short-term (i.e. 6 weeks) assessment of a non-steroidal anti-inflammatory drug (NSAID)-placebo controlled study.

8850. Does the age of onset of rheumatoid arthritis influence phenotype?: a prospective study of outcome and prognostic factors.

作者: C T Pease.;B B Bhakta.;J Devlin.;P Emery.
来源: Rheumatology (Oxford). 1999年38卷3期228-34页
To identify factors affecting prognosis in patients with late-onset rheumatoid arthritis (RA).

8851. Lymphatic microangiopathy of the skin in systemic sclerosis.

作者: A J Leu.;S B Gretener.;S Enderlin.;P Brühlmann.;B A Michel.;O Kowal-Bielecka.;U Hoffmann.;U K Franzeck.
来源: Rheumatology (Oxford). 1999年38卷3期221-7页
The cutaneous capillary lymphatic system in patients with systemic sclerosis was investigated using fluorescence microlymphography. The distal upper limbs of 16 healthy controls (mean age 62.3+/-13.1 yr) and 16 patients with systemic sclerosis (mean age 58.9+/-13.6 yr) were examined and the following parameters were evaluated: (a) single lymphatic capillaries; (b) lymphatic capillary network and cutaneous backflow; (c) extension of the stained lymphatics; (d) diameter of single lymphatic capillaries.

8852. Quantitation of interferon gamma- and interleukin-4-producing T cells in synovial fluid and peripheral blood of arthritis patients.

作者: W L van der Graaff.;A P Prins.;T M Niers.;B A Dijkmans.;R A van Lier.
来源: Rheumatology (Oxford). 1999年38卷3期214-20页
The balance between T cells able to produce interferon gamma (IFN-gamma) (type 1) and interleukin-4 (IL-4) (type 2) is considered to be important in the development of autoimmunity. In this study, we quantitated the percentage of both cell types in synovial fluid (SF) and peripheral blood (PB) of rheumatoid arthritis (RA) patients, non-rheumatoid arthritis patients and healthy controls.

8853. Cytokine production by synovial T cells in rheumatoid arthritis.

作者: G Steiner.;M Tohidast-Akrad.;G Witzmann.;M Vesely.;A Studnicka-Benke.;A Gal.;M Kunaver.;P Zenz.;J S Smolen.
来源: Rheumatology (Oxford). 1999年38卷3期202-13页
To investigate the production of cytokines by T cells in patients with rheumatoid arthritis (RA), reactive arthritis (REA) and osteoarthritis (OA).

8854. Management of steroid-induced osteoporosis: what is the current state of play?

作者: J H Tobias.
来源: Rheumatology (Oxford). 1999年38卷3期198-201页

8855. The current status of ultrasonography in rheumatology.

作者: R J Wakefield.;W W Gibbon.;P Emery.
来源: Rheumatology (Oxford). 1999年38卷3期195-8页

8856. Spondylarthropathy treatment: progress in medical treatment, physical therapy and rehabilitation.

作者: M Dougados.;M Revel.;M A Khan.
来源: Baillieres Clin Rheumatol. 1998年12卷4期717-36页
The monitoring and treatment of the diseases belonging to the concept of spondylarthropathy are related more to their clinical presentation, for example axial versus peripheral involvement, than to the precise diagnosis, for example, ankylosing spondylitis versus psorìatic arthritis. For each clinical presentation the treatment comprises local and systemic routes of administration but also drug and non-drug therapies.

8857. Spondyloarthritides in females.

作者: J T Gran.;M Ostensen.
来源: Baillieres Clin Rheumatol. 1998年12卷4期695-715页
Few studies have been performed regarding clinical, radiological and prognostic features of females with spondyloarthropathies other than ankylosing spondylitis (AS). In AS, clinical manifestations appear similar in men and women, whereas radiological features appear more frequent and severe in males. However, no consistent differences in outcome and mortality between men and women have been disclosed. Although fetal outcome is not compromised in women with spondyloarthropathy (SpA), the interaction of pregnancy and SpA has been studied in detail only in AS. Spinal disease is unchanged while peripheral arthritis and uveitis are suppressed during childbearing. Due to possible maternal and fetal side-effects, NSAIDs must be discontinued during the last 8 weeks of pregnancy, but during lactation several NSAIDs can be used. Treatment with sulphasalazine is compatible with pregnancy and lactation. Children of AS patients exhibit a slightly increased risk of developing SpA later in life.

8858. Measures of outcome in ankylosing spondylitis and other spondyloarthritides.

作者: D M van der Heijde.;S van der Linden.
来源: Baillieres Clin Rheumatol. 1998年12卷4期683-93页
This chapter describes core sets that can be used in the assessment of ankylosing spondylitis and other spondyloarthritides. Various core sets are described for the evaluation of disease-controlling antirheumatic therapy, symptom-modifying antirheumatic drugs and physical therapy, or for use in clinical record keeping. These core sets describe domains and also give advice on specific instruments. The value of spinal mobility and acute-phase reactants in the assessment of ankylosing spondylitis in AS are described in more detail. The available radiological scoring methods are discussed.

8859. Enthesiopathy: clinical manifestations, imaging and treatment.

作者: I Olivieri.;L Barozzi.;A Padula.
来源: Baillieres Clin Rheumatol. 1998年12卷4期665-81页
Enthesitis is a distinctive pathological feature of spondyloarthropathy and may involve synovial joints, cartilaginous joints, syndesmoses and extra-articular entheses. This review focuses on peripheral extra-articular enthesitis which is a clinical hallmark of spondyloarthropathy. The entheses of the lower limbs are more frequently involved than those of the upper limbs, and heel enthesitis is the most frequent. Entheseal pain may be mild or moderate as well as severe and disabling. Peripheral enthesitis may be observed in all forms of spondyloarthropathy, including the undifferentiated ones, and may for a long time be the only long-standing clinical manifestation of the B27-associated disease process. Various imaging methods have been suggested for studying peripheral enthesitis. Ultrasonography and magnetic resonance imaging are the most useful because they may show alterations of the structures involved. Therapy of peripheral enthesitis consists of NSAIDs, orthoses and physical therapy. Steroid injections, second line drugs such as sulphasalazine and radiotherapy are reserved for more severe cases.

8860. The spectrum of skin, mucosa and other extra-articular manifestations.

作者: J Angulo.;L R Espinoza.
来源: Baillieres Clin Rheumatol. 1998年12卷4期649-64页
The seronegative spondyloarthropathies appear to be the genetically predisposed host's clinical expression to acute, subacute or chronic reaction to the invasion by environmental microorganisms. In the ensuing days or weeks, depending on the infectious load, clinical manifestations may occur ranging from constitutional complaints such as fever, to a variety of symptoms and/or signs related to the portal of entry-intestinal, genitourinary or respiratory. Within weeks or months, the initial or other target organs, such as the mucocutaneous, ocular and cardiovascular systems, may develop an acute reaction of greater or lesser specificity regarding the triggering agent (oral ulcers, circinate balanitis, erythema nodosum, acute anterior uveitis, pericarditis, heart blocks). Lastly, many years later, a minority of patients, probably those with a large genetic component, exhibit a spectrum of clinical manifestations related to those organs, with a chronic or recurrent course. Acute clinical manifestations--reactive arthritis--are prominent in the initial phase of the clinical spectrum, while chronic manifestations--ankylosing spondylitis--are seen at the other end of the spectrum.
共有 10420 条符合本次的查询结果, 用时 3.6751524 秒