Immunohistochemical characterization of granulomatosis with polyangiitis exhibiting spontaneous regression | Zendy

Yasuhiro Masuta | Zendy; Yoriaki Komeda | Zendy; Ikue Sekai | Zendy; Akane Hara | Zendy; Masayuki Kurimoto | Zendy; Keisuke Yoshikawa | Zendy; Yasuo Otsuka | Zendy; Ryutaro Takada | Zendy; Tomoe Yoshikawa | Zendy; Ken Kamata | Zendy; Kosuke Minaga | Zendy; Osamu Maenishi | Zendy; Tomohiro Watanabe | Zendy; Masatoshi Kudo | Zendy

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Immunohistochemical characterization of granulomatosis with polyangiitis exhibiting spontaneous regression

Author(s) -

Yasuhiro Masuta,

Yoriaki Komeda,

Ikue Sekai,

Akane Hara,

Masayuki Kurimoto,

Keisuke Yoshikawa,

Yasuo Otsuka,

Ryutaro Takada,

Tomoe Yoshikawa,

Ken Kamata,

Kosuke Minaga,

Osamu Maenishi,

Tomohiro Watanabe,

Masatoshi Kudo

Publication year - 2021

Publication title -

asian pacific journal of allergy and immunology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.405

H-Index - 33

ISSN - 0125-877X

DOI - 10.12932/ap-190221-1073

Subject(s) - granulomatosis with polyangiitis , cd68 , pathology , proteinase 3 , inflammation , microscopic polyangiitis , cd20 , medicine , lung , immunohistochemistry , vasculitis , cd3 , antibody , immune system , myeloperoxidase , immunology , cd8 , disease

Granulomatosis with polyangiitis (GPA) is characterized by granulomatous inflammation, vasculitis, and elevated levels of serum proteinase 3 (PR3)-anti-neutrophil cytoplasmic antibody (PR3-ANCA).

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