Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Kenneth T, Calamia"'
Publikováno v:
Rheumatology International. 43:763-769
Musculoskeletal manifestations of Histoplasma capsulatum infection are uncommon but can mimic inflammatory arthritis. Early diagnosis of this complication is of critical importance in the era of potent immunosuppression for rheumatologic diseases. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c652242280dd80e58bc0a0c221e8f8b7
https://doi.org/10.1007/s00296-021-04912-5
https://doi.org/10.1007/s00296-021-04912-5
Autor:
Florentina Berianu, Madeleine E. Allman, Teresa A. Rummans, Ronald R. Butendieck, Stephanie L. Hines, Fernando A. Rivera, Andy Abril, Shehzad K. Niazi, Barbara K. Bruce, Kenneth T. Calamia, Benjamin Wang
Publikováno v:
JCR: Journal of Clinical Rheumatology. 27:e496-e500
OBJECTIVE The current study was designed to evaluate the translation of clinical trial outcomes and clinical guidelines for the treatment of fibromyalgia (FM) into an intensive multicomponent clinical program embedded in routine care delivery. The st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06b18414255eb0b7f646126a2a69800f
https://doi.org/10.1097/rhu.0000000000001555
https://doi.org/10.1097/rhu.0000000000001555
Publikováno v:
International Journal of Rheumatic Diseases. 24:721-723
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68de3c0ab69e3df765c540d5dd7e7f4b
https://doi.org/10.1111/1756-185x.14099
https://doi.org/10.1111/1756-185x.14099
Autor:
Peter A. Merkel, Randall M. Stevens, Lilia Pineda, Ziqi Liu, Yusuf Yazici, Kenneth T. Calamia, Gulen Hatemi, Melike Melikoglu, Cengiz Korkmaz, Cem Mat, Hasan Yazici, Recep Tunc, Banu Turgut Ozturk
Publikováno v:
New England Journal of Medicine. 372:1510-1518
Oral ulcers, the hallmark of Behçet's syndrome, can be resistant to conventional treatment; therefore, alternative agents are needed. Apremilast is an oral phosphodiesterase-4 inhibitor that modulates several inflammatory pathways.We conducted a pha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df26c9d3e42685cde99e766e8c762acb
https://doi.org/10.1056/nejmoa1408684
https://doi.org/10.1056/nejmoa1408684
Autor:
F. Ramos, Ahmadreza Jamshidi, Carlo Salvarani, Khalifa E. Sharquie, M. Bastos, J. E. Crook, A. V. Elonakov, J. Graña Gil, C. Resende, I. Ben Ghorbel, Ali Akbar Haghdoost, Michael Schirmer, M. Sliti-Khanfir, Samir H. Assaad-Khalil, J. A. Correia, Athanassios Kyrgidis, Nicolò Pipitone, R. M. Hayani, Bahar Sadeghi-Abdollahi, Kenneth T. Calamia, E. Ben-Chetrit, Z. S. Alekberova, N. Ziaei, Ashok Kumar, M. V. De Queiroz, Zilong Zhang, K. Elmuntaser, Hormoz Shams, Wafa Madanat, L. Carvalho, Y. Dong, WenChieh Chen, Phaedon G. Kaklamanis, Ayşe Boyvat, Habib Houman, J. Vaz Patto, Abdolhadi Nadji, C. Vasconcelos, Joana Vedes, Shigeaki Ohno, F. Paixão-Duarte, Christos C. Zouboulis, M. Akhlagi, Kenichi Namba, M. J. Serra, T. Tribolet De Abreu, J. Crespo, E. Arromdee, Cheyda Chams-Davatchi, C. M. Rosa, Y. K. Cheng, T. Tzellos, M. Baltaci, Bertrand Wechsler, A. Altenburg, Farhad Shahram, A. A. Ali, A. Al-Dalaan, I. Olivieri, Fereydoun Davatchi, Carlos Tadeu dos Santos Dias, A. R. Isayeva, S. Benamour
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 28:338-347
Objective Behcet's disease (BD) is a chronic, relapsing, inflammatory vascular disease with no pathognomonic test. Low sensitivity of the currently applied International Study Group (ISG) clinical diagnostic criteria led to their reassessment. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6ef7ce594547ddb1e368df05e37484
https://doi.org/10.1111/jdv.12107
https://doi.org/10.1111/jdv.12107
Publikováno v:
Current Opinion in Rheumatology. 23:24-31
Large vessel vasculitis occurs in a subgroup of patients with Behçet's disease who are at high risk for disease-related morbidity and mortality. Recognition of patients at risk, early detection of vasculitis, and aggressive treatment are essential f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6198fc16b8dee3f9a107a02545cfabe6
https://doi.org/10.1097/bor.0b013e3283410088
https://doi.org/10.1097/bor.0b013e3283410088
Autor:
Eric L. Matteson, Cynthia S. Crowson, Carlo Salvarani, Dylan V. Miller, Aaron W. Broadwell, Gene G. Hunder, Kenneth T. Calamia, Kenneth J. Warrington
Publikováno v:
Rheumatology. 49:1326-1335
Objective. To describe the clinical features and outcomes of patients with localized vasculitis of the gastrointestinal tract (LVGT). Methods. Medical records of 608 patients diagnosed with vasculitis involving the intra-abdominal vasculature and/or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb4e7a8a78ea0bb4cbc66d26401fc07
https://doi.org/10.1093/rheumatology/keq093
https://doi.org/10.1093/rheumatology/keq093
Autor:
Cynthia S. Crowson, Hilal Maradit Kremers, Kenneth T. Calamia, Murat Icen, Sherine E. Gabriel, Floranne C. Wilson
Publikováno v:
Arthritis & Rheumatism. 61:600-604
Objective Behcet's disease (BD) is a rare, multisystem inflammatory disorder of unknown cause. Although well-documented in Eastern populations, epidemiologic data is scarce in North American countries. Here we describe the incidence and prevalence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d874ba14b229a787e810e99241f163
https://doi.org/10.1002/art.24423
https://doi.org/10.1002/art.24423
Publikováno v:
Current Rheumatology Reports. 10:349-355
Behçet's disease (BD) is a chronic, multisystem, inflammatory disorder that is classified among the systemic vasculitidies. Its cause has yet to be determined, but genetic and environmental factors and immune dysregulation are thought to play a role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a2a51fcbb88301392b16dd8864e18c0
https://doi.org/10.1007/s11926-008-0057-y
https://doi.org/10.1007/s11926-008-0057-y
Publikováno v:
Annals of Nuclear Medicine. 22:87-92
Idiopathic retroperitoneal fibrosis is an uncommon disease characterized by periaortic inflammation with gradual fibrosis and distortion of retroperitoneal structures such as the ureter. Several earlier case reports have documented hypermetabolic ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e63e3c0f1db7839f5be17a3ec0fa8a06
https://doi.org/10.1007/s12149-007-0077-0
https://doi.org/10.1007/s12149-007-0077-0