Zobrazeno 1 - 10
of 105
pro vyhledávání: '"granulomatous polyangiitis"'
Autor:
Hao Li, Liyuan Yang
Publikováno v:
Asian Journal of Surgery, Vol 47, Iss 8, Pp 3595-3596 (2024)
Externí odkaz:
https://doaj.org/article/9d5559be16dc4357a1986f793f9f30e8
Publikováno v:
Open Life Sciences, Vol 18, Iss 1, Pp 572-8 (2023)
Granulomatous polyangiitis (GPA) is a rare systemic autoimmune vasculitis disease that is highly correlated with anti-neutrophil cytoplasmic antibodies (ANCAs). It was formerly called as “Wegener’s granulomatosis.” The clinical manifestations a
Externí odkaz:
https://doaj.org/article/9d838bf7026c40bab94412f353958b0c
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Granulomatous polyangiitis (GPA) is a rare autoimmune disease that can involve multiple systems throughout the body, including the ear, nose, upper and lower respiratory tracts. It is classified as an antineutrophil cytoplasmic antibody (ANCA)-associ
Externí odkaz:
https://doaj.org/article/d4e787d1b843492c85f57d8934441cbe
Publikováno v:
Case Reports in Gastroenterology, Vol 17, Iss 1, Pp 155-159 (2023)
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis of small to medium vessels. Gastrointestinal involvement is uncommon and is associated with higher mortality. Treatment is based on empiric evidence. In this article,
Externí odkaz:
https://doaj.org/article/2ec5770651634629a957743ce2d4131c
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Granulomatous polyangiitis (GPA) is a rare multisystem autoimmune disease of unknown aetiology that is pathologically characterised by necrotising vasculitis, tissue necrosis and granulomatous inflammation, typically in the presen
Externí odkaz:
https://doaj.org/article/4827922343414e7e996134861abb81cf
Akademický článek
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Akademický článek
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Publikováno v:
Genel Tıp Dergisi, Vol 29, Iss 4, Pp 210-213 (2019)
Sjögren Sendromu SjS öncelikle gözyaşı ve tükrük bezleri olmak üzere tüm ekzokrin bezlerin lenfositit infiltrasyonu ile karakterize kronik, sistemik ve otoimmün bir hastalıktır. Kserostomi ve kseroftalmi tablosu hastalığın ana belirtis
Externí odkaz:
https://doaj.org/article/6ae6006aa3c1415c9a64d2f42cde2e4c
Autor:
Tahsin KARAASLAN, Cumali KARATOPRAK
Publikováno v:
Bezmiâlem Science, Vol 7, Iss 3, Pp 255-258 (2019)
Granulomatosis polyangiitis (GPA) is a systemic, necrotizing, granulomatous, antineutrophil cytoplasmic antibody (ANCA) -associated vasculitis that affects small and medium arteries, mainly affecting the upper and lower respiratory tract and the kidn
Externí odkaz:
https://doaj.org/article/833813ad09834454b6c5f1a82847346b
Autor:
Koichiro Takahashi, Hironori Sadamatsu, Hiroki Tashiro, Go Kato, Masaru Uchida, Naoko Sueoka‐Aragane
Publikováno v:
Respirology Case Reports, Vol 8, Iss 4, Pp n/a-n/a (2020)
Abstract A 51‐year‐old woman was admitted to our hospital for cough, fever, purpura in the legs, and salivary gland swelling. Six years ago, she had been diagnosed with bronchial asthma and was treated with a combination of inhaled corticosteroid
Externí odkaz:
https://doaj.org/article/4696d745d2bc4cdaae7663713ddf5a42