science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/oup/periodical/brheum/2006/volume_45/issue_8/w
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
bibo:Issue
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
work
Issue
New Facet based on Instances of this Class
Attributs
Valeurs
type
work
Issue
Is Part Of
http://hub.abes.fr/oup/periodical/brheum/2006/volume_45
has manifestation of work
http://hub.abes.fr/oup/periodical/brheum/2006/volume_45/issue_8/m/print
http://hub.abes.fr/oup/periodical/brheum/2006/volume_45/issue_8/m/web
Date Copyrighted
2006
Rights
© The Author 2006. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
© Published by Oxford University Press on behalf of the British Society for Rheumatology 2006.
issue
8
is
Is Part Of
of
An electronic logbook for rheumatologists performing musculoskeletal ultrasound
Polymorphisms of the FCRL3 gene in a Spanish population of systemic lupus erythematosus patients
Towards a pro-inflammatory and immunomodulatory emerging role of leptin
Re: Touch screen computer systems in the rheumatology clinic offer a reliable and user-friendly means of collecting quality-of-life and outcome data from patients with rheumatoid arthritis
Mycophenolate mofetil as first-line treatment improves clinically evident early scleroderma lung disease
Against the current—when primary pericardial disease causes rheumatic disease
Iloprost treatment in patients with Raynaud's phenomenon secondary to systemic sclerosis and the quality of life: a new therapeutic protocol
BSR & BHPR, BOA, RCGP and BSAC guidelines for management of the hot swollen joint in adults
Detection of tuberculosis by extensive screening in a patient with rheumatoid arthritis prior to anti-TNF-α therapy
Imbalance of Th1/Th2 transcription factors in patients with lupus nephritis
Moderate and severe neutropenia in patients with systemic lupus erythematosus
Spontaneous pneumothorax are seen in the joint hipermobility syndrome (JHS)
Infliximab as rescue therapy in three cases of paediatric Wegener's granulomatosis
Incidence of cancer in a cohort of patients with primary Sjögren's syndrome
Patients' own ability to assess activity of their rheumatoid arthritis
Estimating the cost and health status consequences of treatment with TNF antagonists in patients with psoriatic arthritis
Touch screen computers in the rheumatology clinic
Gender and socio-economic variations in employment among patients with a diagnosed musculoskeletal disorder: a longitudinal record linkage study in Sweden
Spontaneous pneumothorax are seen in the joint hypermobility syndrome (JHS): reply
Acute progression of interstitial lung disease: a complication of etanercept particularly in the presence of rheumatoid lung and methotrexate treatment
Retinoic acid and oncostatin M combine to promote cartilage degradation via matrix metalloproteinase-13 expression in bovine but not human chondrocytes
The reliability, validity and sensitivity to change of the Chinese version of SF-36 in oriental patients with rheumatoid arthritis
An international consensus survey of the diagnostic criteria for juvenile dermatomyositis (JDM)
Tumour necrosis factor α inhibitors in the treatment of childhood uveitis
A patient-centred approach to drug regulation
Association of HLA-DRB1*13 with susceptibility to uveitis in juvenile idiopathic arthritis in two independent data sets
Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients
Synovial vascular patterns and angiogenic factors expression in synovial tissue and serum of patients with rheumatoid arthritis
The relationship of medical, demographic and psychosocial factors to direct and indirect health utility instruments in rheumatoid arthritis
Macrophage migration inhibitory factor and glucocorticoid sensitivity
Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura in the setting of adult-onset Still's disease
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata