Advances in Takayasu arteritis: An Asia Pacific perspective
Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There have been several developments in the field of Takayasu arteritis in relation to genetics, classification, clinical features, imaging, disea...
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Published in | Frontiers in medicine Vol. 9; p. 952972 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
15.08.2022
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Abstract | Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There have been several developments in the field of Takayasu arteritis in relation to genetics, classification, clinical features, imaging, disease activity assessment and management and much of these works have been done in the Asia Pacific region. We will be discussing selected few in the current review. |
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AbstractList | Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There have been several developments in the field of Takayasu arteritis in relation to genetics, classification, clinical features, imaging, disease activity assessment and management and much of these works have been done in the Asia Pacific region. We will be discussing selected few in the current review. Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There have been several developments in the field of Takayasu arteritis in relation to genetics, classification, clinical features, imaging, disease activity assessment and management and much of these works have been done in the Asia Pacific region. We will be discussing selected few in the current review.Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There have been several developments in the field of Takayasu arteritis in relation to genetics, classification, clinical features, imaging, disease activity assessment and management and much of these works have been done in the Asia Pacific region. We will be discussing selected few in the current review. |
Author | Harigai, Masayoshi Danda, Debashish Tian, Xinping Manikuppam, Prathyusha |
AuthorAffiliation | 3 Division of Epidemiology and Pharmacoepidemiology of Rheumatic Diseases, Institute of Rheumatology, Tokyo Women's Medical University , Tokyo , Japan 1 Department of Clinical Immunology and Rheumatology, Christian Medical College and Hospital , Vellore , India 2 Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Peking Union Medical College Hospital (PUMCH) , Beijing , China |
AuthorAffiliation_xml | – name: 2 Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Peking Union Medical College Hospital (PUMCH) , Beijing , China – name: 1 Department of Clinical Immunology and Rheumatology, Christian Medical College and Hospital , Vellore , India – name: 3 Division of Epidemiology and Pharmacoepidemiology of Rheumatic Diseases, Institute of Rheumatology, Tokyo Women's Medical University , Tokyo , Japan |
Author_xml | – sequence: 1 givenname: Debashish surname: Danda fullname: Danda, Debashish – sequence: 2 givenname: Prathyusha surname: Manikuppam fullname: Manikuppam, Prathyusha – sequence: 3 givenname: Xinping surname: Tian fullname: Tian, Xinping – sequence: 4 givenname: Masayoshi surname: Harigai fullname: Harigai, Masayoshi |
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CitedBy_id | crossref_primary_10_1016_j_heliyon_2023_e13099 crossref_primary_10_17650_1818_8338_2023_17_1_K666 crossref_primary_10_1111_1756_185X_15314 crossref_primary_10_1093_cei_uxae095 crossref_primary_10_1001_jamaophthalmol_2024_5542 crossref_primary_10_1007_s40336_023_00586_0 crossref_primary_10_1021_cbmi_4c00117 crossref_primary_10_3390_biomedicines11082207 crossref_primary_10_1007_s12070_024_04938_8 crossref_primary_10_69944_pjc_9fe715c7c9 crossref_primary_10_1002_acr2_11766 |
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Copyright | Copyright © 2022 Danda, Manikuppam, Tian and Harigai. Copyright © 2022 Danda, Manikuppam, Tian and Harigai. 2022 Danda, Manikuppam, Tian and Harigai |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Reviewed by: Florence A. Aeschlimann, University Children's Hospital Basel, Switzerland; Haner Direskeneli, Marmara University, Turkey These authors have contributed equally to this work and share first authorship Edited by: Peter Mandl, Medical University of Vienna, Austria This article was submitted to Rheumatology, a section of the journal Frontiers in Medicine |
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Snippet | Takayasu Arteritis (TA) is a rare form of chronic granulomatous large vessel vasculitis that is more common in Asia compared to other parts of the world. There... |
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