Littérature scientifique sur le sujet « Enthesitis-related arthritis »

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Articles de revues sur le sujet "Enthesitis-related arthritis"

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Hahn, Youn-Soo. « Enthesitis-related Arthritis ». Journal of Rheumatic Diseases 25, no 4 (2018) : 221. http://dx.doi.org/10.4078/jrd.2018.25.4.221.

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Aggarwal, Amita, et Durga Prasanna Misra. « Enthesitis-related arthritis ». Clinical Rheumatology 34, no 11 (2 août 2015) : 1839–46. http://dx.doi.org/10.1007/s10067-015-3029-4.

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Shenoy, Sajjan, et Amita Aggarwal. « 268. Subclinical Sonologic Enthesitis in Juvenile Idiopathic Arthritis–Enthesitis-Related Arthritis ». Rheumatology 53, suppl_1 (avril 2014) : i159—i160. http://dx.doi.org/10.1093/rheumatology/keu123.002.

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Rosenthal, Ayelet, et Ginger Janow. « Enthesitis-Related Juvenile Idiopathic Arthritis ». Pediatrics in Review 40, no 5 (mai 2019) : 256–58. http://dx.doi.org/10.1542/pir.2017-0177.

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Mistry, Rutviz Rajendra, Pallavi Patro, Vikas Agarwal et Durga Prasanna Misra. « Enthesitis-related arthritis : current perspectives ». Open Access Rheumatology : Research and Reviews Volume 11 (janvier 2019) : 19–31. http://dx.doi.org/10.2147/oarrr.s163677.

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Weiss, Pamela F. « Update on enthesitis-related arthritis ». Current Opinion in Rheumatology 28, no 5 (septembre 2016) : 530–36. http://dx.doi.org/10.1097/bor.0000000000000313.

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Weiss, Pamela F., Andrew J. Klink, Edward M. Behrens, David D. Sherry, Terri H. Finkel, Chris Feudtner et Ron Keren. « Enthesitis in an inception cohort of enthesitis-related arthritis ». Arthritis Care & ; Research 63, no 9 (29 août 2011) : 1307–12. http://dx.doi.org/10.1002/acr.20508.

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Singh, Yogesh Preet, Vikas Agarwal, Narendra Krishnani et Ramnath Misra. « Enthesitis-related arthritis in Kikuchi–Fujimoto disease ». Modern Rheumatology 18, no 5 (octobre 2008) : 492–95. http://dx.doi.org/10.3109/s10165-008-0076-6.

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ENAZI, ABDULLATIF AL, KIM MORISHITA, ROBYN A. CAIRNS, LORI TUCKER, DAVID CABRAL, ROSS PETTY et JAIME GUZMAN. « Early Atlantoaxial Subluxation in Enthesitis-related Arthritis ». Journal of Rheumatology 41, no 6 (juin 2014) : 1190–91. http://dx.doi.org/10.3899/jrheum.131206.

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Kan, J. Herman. « Juvenile idiopathic arthritis and enthesitis-related arthropathies ». Pediatric Radiology 43, S1 (mars 2013) : 172–80. http://dx.doi.org/10.1007/s00247-012-2586-9.

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Thèses sur le sujet "Enthesitis-related arthritis"

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PAGNINI, ILARIA. « biologic therapy in children with enthesitis-related arthritis the fist year after disease onset ». Doctoral thesis, 2017. http://hdl.handle.net/2158/1077517.

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ABSTRACT Objective. There is scant evidence to guide physicians in the choice of one therapeutic agent or combination over another to treat children and adolescents with enthesites-re lated arthritis (ERA). Clinicians not only need to know about the efficacy of disease-modifying anti-rheumatic drugs (DMARDs) and biologic as stand-alone therapy ver sus placebo, but also how they work in combination and in comparison to one another. The main objective of the study is to characterized the effec tive of biologic exposure in children with ERA over the first year after diagnosis. Methods. We conduced a multicenter retrospective study of children diagnosed with ERA followed in several hospital: Children’s Hospital of Philadelphia, Alabama Children’s Hospital, Cincinnati Children’s Hospital, Texas Scottish Rite Hospital for Children and Meyer Children’s Hospital. We estimated the effect of biologic therapy on clinical pa rameters (active joint count, tender enthesis count, develo pment of sacroiliitis), physician disease activity assessment, and patient-reported pain and global assessment of disease activity over the first year after diagnosis using a weighted repeated measures approach. Results. During the study period, 218 newly diagnosed ERA patients had a total of 968 clinic visits the first year di sease onset. 35 (16.1%), 70 (32.1%) and 56 (25.7%) were treated with biologic, DMARD monotherapy, or both, re spectively during the first year after diagnosis. Over the first year after disease onset, use of a biologic was significantly associated with less pain (p=0.03) and improved disease ac tivity as measured by the JADAS-3 (p=0.02). Use of a bio logic, versus no biologic, was associated with a significant greater negative slope (or faster change over the time) in tender entheses count (p<0.01). Conclusion. During the first year after diagnosis, biologic exposure was associated with benefits for several clinically meaningful outcomes in children with enthesites-related ar thritis
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Livres sur le sujet "Enthesitis-related arthritis"

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Rudwaleit, Martin. Enthesitis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0054.

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Enthesitis is one of the key manifestations of spondyloarthritides (SpA) including ankylosing spondylitis (AS) and psoriatic arthritis. Enthesitis can occur alone or in combination with peripheral arthritis, sacroiliitis, or spondylitis. The inflammatory process is typically located at the insertion of the enthesis or ligament to bone, often resulting in osteitis as well. Because of its anatomical and functional complexity the term 'enthesis organ' has been coined. Biomechanical stress applied to the enthesis seems to play an important role for the occurrence of enthesitis in genetically predisposed individuals. Ultrasound imaging of peripheral entheses reveals enthesis abnormalities including entheseal calcification, bony erosion, or bony proliferation. Power Doppler signals demonstrating increased vascularization of inflamed entheses at the insertional site appear to be the most characteristic finding for enthesitis, yet study results are conflicting. Enthesitis-related osteitis and enthesitis at the spine is best visualized by MRI. Enthesitis may resolve spontaneously or may run a chronic course. Standard treatment includes local steroid injections, non-steroidal anti-inflammatory drugs (NSAIDs), and physical therapy. There is little evidence for the efficacy of disease-modifying anti-rheumatic drugs (DMARDs) in enthesitis. In contrast, anti-TNF agents have proven efficacy, and their use in treatment-resistant enthesitis is recommended in the Assessment of SpondyloArthritis international Society (ASAS)/European League Against Rheumatism (EULAR) recommendations for the management of AS and axial SpA and in the EULAR recommendations for psoriatic arthritis.
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Rudwaleit, Martin. Enthesitis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0054_update_002.

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Enthesitis is one of the key manifestations of spondyloarthritis (SpA) including ankylosing spondylitis (AS) and psoriatic arthritis. Enthesitis can occur alone or in combination with peripheral arthritis, sacroiliitis, or spondylitis. The inflammatory process is typically located at the insertion of the enthesis or ligament to bone, often resulting in osteitis as well. Because of its anatomical and functional complexity the term ’enthesis organ’ has been coined. Biomechanical stress applied to the enthesis seems to play an important role for the occurrence of enthesitis in genetically predisposed individuals. Ultrasound imaging of peripheral entheses reveals enthesis abnormalities including entheseal calcification, bony erosion, or bony proliferation. Power Doppler signals demonstrating increased vascularization of inflamed entheses at the insertional site appear to be the most characteristic finding for enthesitis, yet study results are conflicting. Enthesitis-related osteitis and enthesitis at the spine is best visualized by MRI. Enthesitis may resolve spontaneously or may run a chronic course. Standard treatment includes local steroid injections, non-steroidal anti-inflammatory drugs (NSAIDs), and physical therapy. There is little evidence for the efficacy of disease-modifying antirheumatic drugs (DMARDs) in enthesitis. In contrast, anti-TNF agents have proven efficacy, and their use in treatment-resistant enthesitis is recommended in the Assessment of SpondyloArthritis international Society (ASAS)/European League Against Rheumatism (EULAR) recommendations for the management of AS and axial SpA and in the EULAR recommendations for psoriatic arthritis.
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Burgos-Vargas, Ruben, et Shirley M. L. Tse. Juvenile-onset spondyloarthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198734444.003.0015.

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Juvenile-onset spondyloarthritis (JoSpA) refers to the group of HLA-B27-associated paediatric rheumatic diseases that involves the synovium and entheses of peripheral joints in the initial years and, in some patients, the sacroiliac and spinal joints several years later. Patients with JoSpA may also have extra-articular manifestations, including anterior uveitis, psoriasis and inflammatory bowel disease (IBD), and this represents a disease continuum with adult-onset SpA. JoSpA might include patients with enthesitis-related arthritis (ERA) and PsA categories of juvenile idiopathic arthritis (JIA), according to the International League of Associations for Rheumatology (ILAR). The opposite does not occur, since ILAR JIA classification does not allow the possibility of clinical overlapping among the different categories, one of the most important features of SpA.
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Chapitres de livres sur le sujet "Enthesitis-related arthritis"

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Tse, Shirley M. L., et Ross E. Petty. « Enthesitis Related Arthritis ». Dans Textbook of Pediatric Rheumatology, 238–55. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-24145-8.00019-3.

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Petty, Ross E., et James T. Cassidy. « ENTHESITIS-RELATED ARTHRITIS (JUVENILE ANKYLOSING SPONDYLITIS) ». Dans Textbook of Pediatric Rheumatology, 272–86. Elsevier, 2011. http://dx.doi.org/10.1016/b978-1-4160-6581-4.10017-2.

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Rudwaleit, Martin. « Enthesitis ». Dans Oxford Textbook of Rheumatology, 398–403. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0054_update_003.

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Enthesitis is one of the key manifestations of spondyloarthritis (SpA) including ankylosing spondylitis (AS) and psoriatic arthritis. Enthesitis can occur alone or in combination with peripheral arthritis, sacroiliitis, or spondylitis. The inflammatory process is typically located at the insertion of the enthesis or ligament to bone, often resulting in osteitis as well. Because of its anatomical and functional complexity the term ’enthesis organ’ has been coined. Biomechanical stress applied to the enthesis seems to play an important role for the occurrence of enthesitis in genetically predisposed individuals. Ultrasound imaging of peripheral entheses reveals enthesis abnormalities including entheseal calcification, bony erosion, or bony proliferation. Power Doppler signals demonstrating increased vascularization of inflamed entheses at the insertional site appear to be the most characteristic finding for enthesitis, yet study results are conflicting. Enthesitis-related osteitis and enthesitis at the spine is best visualized by MRI. Enthesitis may resolve spontaneously or may run a chronic course. Standard treatment includes local steroid injections, non-steroidal anti-inflammatory drugs (NSAIDs), and physical therapy. There is little evidence for the efficacy of disease-modifying antirheumatic drugs (DMARDs) in enthesitis. In contrast, anti-TNF agents and other biologics have proven efficacy, and their use in treatment-resistant enthesitis is recommended in the Assessment of SpondyloArthritis international Society (ASAS)/European League Against Rheumatism (EULAR) recommendations for the management of AS and axial SpA and in the EULAR recommendations for psoriatic arthritis.
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Clunie, Gavin, Nick Wilkinson, Elena Nikiphorou et Deepak R. Jadon. « The spondyloarthritides including psoriatic arthritis ». Dans Oxford Handbook of Rheumatology, sous la direction de Gavin Clunie, Nick Wilkinson, Elena Nikiphorou et Deepak R. Jadon, 293–320. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198728252.003.0008.

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The Oxford Handbook of Rheumatology, 4th edition, includes a chapter on spondyloarthritis (SpA) conditions. These conditions are axial spondyloarthritis, including ankylosing spondylitis, psoriatic arthritis, reactive arthritis, and inflammatory bowel disease-related arthritis. It summarizes evidence for pathogenetic mechanisms either common to all conditions, or specific for each condition, highlights current disease classifications, and emphasizes clinical features common to all SpAs, such as inflammatory back pain and enthesitis. There is an expanded section on treatments including biologic disease-modifying antirheumatic drugs (bDMARDs; ‘biologics’) such as anti-tumour necrosis factor-α‎, ustekinumab, and secukinumab, and new to this edition of the Handbook, an expanded section on juvenile spondyloarthritis.
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Clunie, Gavin, Nick Wilkinson, Elena Nikiphorou et Deepak R. Jadon. « Common upper limb musculoskeletal lesions ». Dans Oxford Handbook of Rheumatology, sous la direction de Gavin Clunie, Nick Wilkinson, Elena Nikiphorou et Deepak R. Jadon, 595–604. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198728252.003.0020.

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This chapter introduces readers to some common upper limb musculoskeletal lesions, including subacromial (shoulder) impingement syndrome, adhesive capsulitis, and lateral epicondylitis (tennis elbow). The epidemiology, aetiopathogenesis, clinical presentation, and management of these conditions are presented. Algorithms for their management are provided. Other disorders presenting with a subacromial impingement pattern of pain are detailed and optimal diagnostic imaging methods proposed. These include supraspinatus/cuff tendonitis, subacromial bursitis, rotator cuff tear, long head of biceps tendonitis, osteophyte impingement on the rotator cuff tendon, glenohumeral instability due to labral trauma (e.g. SLAP lesion), arthritis of the glenohumeral joint, enthesitis related to spondyloarthritis, and lesions at the suprascapular notch.
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Ruperto, Nicolino, et Angelo Ravelli. « Principles of management of juvenile idiopathic arthritis ». Dans Oxford Textbook of Rheumatology, 725–33. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0096.

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The management of juvenile idiopathic arthritis (JIA) is based on a combination of pharmacological interventions, physical and occupational therapy, and psychosocial support. Ideally, the management is conducted by a multidisciplinary team composed by a paediatric rheumatologist, specialist nurse, physical therapist, occupational therapist, and psychologist. The treatment is aimed to achieve disease control, to relieve pain, to foster normal nutrition and growth, to maintain physical and psychological well-being, and to prevent long-term damage related to the disease or its therapy. First-line pharmacological interventions are based on non-steroidal anti-inflammatory drugs and intra-articular corticosteroids. Patients who are refractory to these therapies are candidates to receive disease-modifying anti-rheumatic medications, namely methotrexate or, in case of enthesitis-related arthritis, sulfasalazine. If therapeutic response is inadequate or suboptimal, the introduction of a biologic response modifier is considered. Systemic corticosteroids are used in selected instances, which include the management of extra-articular manifestations of systemic arthritis or the achievement of quick disease control while are awaiting the full therapeutic effect of a disease-modifying agent in patients with severe polyarthritis. To help physician select the safest and most effective treatment for JIA, the American College of Rheumatology (ACR) has issued a set of recommendations that were meant to be as evidence based as possible. The British Society for Paediatric and Adolescent Rheumatology (BSPAR) has developed the standards of care for patients with JIA, which are aimed to help the paediatric rheumatology teams to improve the service they provide.
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Stefan Cristian, Dinescu, Ionescu Razvan Adrian, Popoviciu Horatiu Valeriu, Avram Claudiu et Vreju Ananu Florentin. « Musculoskeletal and Nerve Ultrasonography ». Dans Ultrasound Imaging - Current Topics [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.102640.

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Musculoskeletal ultrasound had gained more and more importance lately and there is no doubt now about its role in the diagnosis and management of rheumatic diseases such as rheumatoid arthritis, spondyloarthritis, osteoarthritis and crystal related arthropathies. We can say that now, US is a widely available, non-invasive, and cost-effective technique suitable for the evaluation of the articular and periarticular structures, such as joints, tendons, muscles, ligaments, and bursa. The real-time capabilities of the US allow continuous observation of those structures during movement and of the needle placement during musculoskeletal interventions. More than this, recently, ultrasonography (US) has gained its rights in the evaluation of Sjogren syndrome and giant cell arteritis. Thus, US can detect changes secondary to both inflammatory joint diseases, like synovitis, tenosynovitis or enthesitis, and to degenerative disease, like osteophytes or tendinosis. US can identify calcium pyrophosphate and urate deposits at the level of the cartilage and tendons and to recognize the changes at the level of the salivary glands in the context of the Sjogren’s syndrome and the ones at the level of the temporal artery, secondary to giant cell arteritis.
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Braun, J., et J. Sieper. « Ankylosing spondylitis, other spondyloarthritides, and related conditions ». Dans Oxford Textbook of Medicine, 3603–16. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199204854.003.1906.

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The spondyloarthritides are a group of inflammatory rheumatic diseases with predominant involvement of axial and peripheral joints and entheses, together with other characteristic clinical features, including inflammatory back pain, sacroiliitis, peripheral arthritis (mainly in the legs), enthesitis, dactylitis, preceding infection of the urogenital/gastrointestinal tract, psoriatic skin lesions, Crohn-like gut lesions, anterior uveitis, and a family history of Spondyloarthritis. They are the second most frequent inflammatory rheumatic diseases after rheumatoid arthritis....
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Braun, Jürgen, et Joachim Sieper. « Spondyloarthritis and related conditions ». Dans Oxford Textbook of Medicine, sous la direction de Richard A. Watts, 4441–56. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0447.

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The spondyloarthritides are a group of common inflammatory rheumatic diseases with predominant involvement of axial and peripheral joints and entheses, together with other characteristic clinical features, including inflammatory back pain, sacroiliitis, peripheral arthritis (mainly in the legs), enthesitis, dactylitis, preceding infection of the urogenital/gastrointestinal tract, psoriatic skin lesions, Crohn-like gut lesions, anterior uveitis, and a family history of spondyloarthritis (SpA). Five subsets can be distinguished on clinical grounds: (1) axial SpA, including ankylosing spondylitis; (2) reactive (spondylo)arthritis/Reiter’s syndrome; (3) psoriatic (spondylo)arthritis; (4) (spondylo)arthritis associated with inflammatory bowel diseases; and (5) undifferentiated peripheral SpA. Prevalence in any population correlates roughly with that of HLA B27, but the relevance of this to pathogenesis is not known. Another more recent approach is to differentiate the SpA on the basis of the predominant clinical manifestation: predominant axial and/or peripheral SpA.
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Actes de conférences sur le sujet "Enthesitis-related arthritis"

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Katsicas, M., C. Carrara, A. Bernasconi, J. Rossi et R. Russo. « THU0521 Enthesitis-related arthritis : non-peripheral pattern is associated with th17 cells ». Dans Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.6726.

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Silva Veloso, Sarah Polyane, Regiane Duque Minardi Neves, Agatha Siqueira Afonso, Aline Garcia Islabão, Caio Alexandre Zanoni, Cristina Medeiros Ribeiro de Magalhães, Maria Custódia Machado Ribeiro, Marlon Sousa Lopes, Simone de Oliveira Alves et Marne Rodrigues Pereira Almeida. « ADOLESCENT WITH ENTHESITIS-RELATED ARTHRITIS AND PAEDIATRIC MULTISYSTEM INFLAMMATORY SYNDROME TEMPORALLY ASSOCIATED WITH COVID-19 ». Dans Congresso Brasileiro de Reumatologia 2020. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2020.17497.

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Choida, Varvara, Tim Bray, Anna Radziszewska, Corinne Fisher, Coziana Ciurtin, Debajit Sen et Margaret Hall-Craggs. « AB0950 CORRELATION OF QUANTITATIVE MAGNETIC RESONANCE IMAGING BIOMARKERS AND AXIAL PAIN IN ENTHESITIS-RELATED ARTHRITIS PATIENTS ». Dans Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.7742.

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harikrishnan velayudhan, pillai, Rasmi Ranjan Sahoo, Saumya Ranjan Tripathy, Urmila Dhakad, Puneet Kumar, Anupam Wakhlu et Siddharth Kumar Das. « FRI0580 ULTRASONOGRAPHY SCORE CORRELATES WITH DISEASE ACTIVITY IN JUVENILE IDIOPATHIC ARTHRITIS – ENTHESITIS RELATED ARTHRITIS – A CROSS SECTIONAL OBSERVATIONAL STUDY FROM INDIA ». Dans Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.2884.

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Fisher, C., D. Eleftheriou, D. Sen et Y. Ioannou. « OP0056 IL-23P19 is up-regulated in monocyte-derived macrophages from HLA B27 positive patients with enthesitis related arthritis ». Dans Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.5004.

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RIOS-NETO, EDUARDO CESAR, MARIANA NOBRE ALMEIDA DIAS, GABRIELA COUTINHO GONDIM JUSTA, LARISSA OLIVEIRA RIBEIRO, LÍLIA TORQUILHO ALMEIDA, JÚLIA COUTO RORIZ LOIOLA, DEYZILENE CARDOSO ARAÚJO et al. « ARE DIAGNOSTIC CRITERIA FOR SPONDYLARTHRITIS SUITABLE TO PATIENTS WITH ENTHESITIS-RELATED ARTHRITIS ? A NINE-YEAR EXPERIENCE OF A PEDIATRIC RHEUMATOLOGY UNIT IN CEARA ». Dans 36º Congresso Brasileiro de Reumatologia. São Paulo : Editora Blucher, 2019. http://dx.doi.org/10.5151/sbr2019-340.

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Foell, D., J. A. Veit, E. Ilsley et K. Abrams. « AB1089 Investigation of the efficacy and safety of secukinumab treatment in juvenile idiopathic arthritis subtypes of juvenile psoriatic and enthesitis-related arthritis : design of a randomised, double-blind, placebo controlled, multicenter study ». Dans Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.2097.

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Fisher, C., D. Eleftheriou, D. Sen et Y. Ioannou. « OP0097 Stimulated monocyte-derived macrophages from patients with enthesitis related arthritis secrete higher levels of il23 and lower levels of interferon gamma compared to healthy controls ». Dans Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.5377.

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Fisher, C., D. Eleftheriou, D. Sen et Y. Ioannou. « FRI0004 Granulocyte macrophage colony stimulating factor is secreted at higher levels from stimulated monocyte-derived macrophages from patients with enthesitis related arthritis and is significantly enhanced by the unfolded protein response ». Dans Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.5457.

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