Results 61 to 70 of about 5,850 (214)
Vasculitides associated with IgG antineutrophil cytoplasmic autoantibodies in childhood [PDF]
Immunoglobulin (Ig)G antineutrophil cytoplasmic autoantibodies are causally associated with necrotizing vasculitides that are characterized immunopathologically by little or no deposition of immunoreactants, such as Wegener granulomatosis, microscopic ...
Bettinelli, Alberto +4 more
core
ABSTRACT Radiotherapy is an important therapeutic modality for advanced hepatocellular carcinoma (HCC), but the limited understanding of radioresistance mechanisms in HCC has hindered its further clinical development. This work aimed to clarify the essential role of Cathepsin C (CTSC) in regulating radioresistance in HCC.
Jiahuan Xu +5 more
wiley +1 more source
Frozen Eye in Granulomatosis with Polyangiitis (Wegener's)
Ocular involvement in Granulomatosis with Polyangiitis (GP or Wegener Granulomatosis) is a potentially serious disease manifestation which needs prompt diagnosis and treatment.
Qin Yan MRCP +2 more
doaj +1 more source
El presente manuscrito se hace con el fin de reportar un caso del tema en mención y realizar una revisión de la literatura disponible más reciente con respecto al diagnóstico y tratamiento. Antecedentes La granulomatosis de Wegener (GW) se caracteriza
José Luis Fabris Vargas +4 more
doaj +1 more source
Granulomatosis With Polyangiitis in Otolaryngologist Practice: A Review of Current Knowledge [PDF]
Granulomatosis with polyangiitis (GPA) is an idiopathic vasculitis of medium and small arteries, characterized by necrotizing granulomatous inflammation. GPA typically affects upper and lower respiratory tract with coexisting glomerulonephritis.
Joanna Wojciechowska +3 more
doaj +1 more source
Types of Angiopathy in Experimental Autoimmune Disease in Rats [PDF]
The purpose and objectives of this work were to study the nature of the heart, lungs and kidneys angiopathy in rats with a model of systemic autoimmune disease, carrying out comparisons of the results with extravasal morphological manifestations of the ...
Iegudina, Y. (Yelizaveta) +3 more
core +2 more sources
Objective Diffuse alveolar hemorrhage (DAH) is a life‐threatening presentation of antineutrophil cytoplasmic antibody–associated vasculitis (AAV). Patients with AAV are at an increased risk of venous thromboembolic events (VTEs). These manifestations can co‐occur; however, the prognosis and management of these patients are poorly understood. Methods In
Elif D. Ediboglu +5 more
wiley +1 more source
Wegener´s granulomatosis in a young patient preceded by localized cutaneous manifestations
Wegener´s granulomatosis (WG) is a rare, systemic vasculitis involving multiple organs. The clinical presentation is highly diverse, and there is considerable risk of mortality if diagnosis and treatment are delayed.
Jesper Smit +3 more
doaj +1 more source
Granulomatosis with Polyangiitis (Wegener's): An alternative name for Wegener's Granulomatosis [PDF]
The Boards of Directors of the American College of Rheumatology, the American Society of Nephrology, and the European League Against Rheumatism recommend a gradual shift from honorific eponyms to disease-descriptive or etiology-based nomenclature.
Falk, R. J. +12 more
openaire +9 more sources
Safety of Immune Checkpoint Inhibitors in Cancer Patients With Preexisting Autoimmune Vasculitis
Objective Immune checkpoint inhibitors (ICIs) are effective cancer therapies but often cause serious immune‐related adverse events (irAEs). Patients with preexisting autoimmune diseases, including vasculitis, are excluded from trials. We aimed to evaluate the frequency, severity, and outcomes of vasculitis flares and irAEs in this population.
Juan Sevillano +4 more
wiley +1 more source

