Results 101 to 110 of about 9,401 (207)
The pathological diagnosis of nerve biopsies: a practical approach [PDF]
, 2016 The approach to the neuropathological assessment of nerve biopsies is the main focus of this review. Nerve biopsies are invasive diagnostic procedures resulting in a permanent neurological deficit, and are therefore carried out only following an in-depth
Brandner, S
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Differences in the frequency of macrophage and t cell markers between focal and crescentic classes of antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis [PDF]
, 2017 Funding/Support This study was supported by Tenovus Scotland/Tayside grant award to DK (Grant # T13/15).Peer reviewedPublisher ...
Bray, Susan E. +2 more
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Orbital inflammatory complications of Crohn’s disease: a rare case series [PDF]
, 2018 Orbital inflammatory disease is a rare ophthalmic manifestation of Crohn’s disease. Inflammation is characteristically non-specific, involving one or multiple structures of the orbit.
Abercrombie, Lorraine +5 more
core +3 more sources
Vasculitis of the upper airways1
Swiss Medical Weekly, 2012 Systemic vasculitides are rare and potentially life-threatening diseases. Granulomatosis with polyangiitis (GPA; formerly Wegener’s granulomatosis) and Churg Strauss syndrome (possibly to be renamed eosinophilic granulomatosis with polyangiitis ...
Christian Pagnoux, Nikolaus E Wolter
doaj +1 more source
Checks and Balances in Autoimmune Vasculitis [PDF]
, 2016 Age-associated changes in the immune system including alterations in surface protein expression are thought to contribute to an increased susceptibility for autoimmune diseases. The balance between the expression of coinhibitory and costimulatory surface
Abdulahad, Wayel H. +6 more
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A case of eosinophilic polyangiitis with granulomatosis that evolved to cardiac arrest due to advanced atrioventricular block [PDF]
, 2023 Cardiac manifestations are the major cause of mortality in patients with eosinophilic granulomatosis with polyangiitis (EGPA). Among these manifestations in EGPA patients, in the literature, there are fewer reports describing bradycardia in EGPA patients
Kaneko, Takeshi +9 more
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Опыт ведения больных с синдромом Чарджа-Стросса [PDF]
, 2018 Our goal was to analyze the possibilities of improving the diagnostics of CSS and to improve the effectiveness of treatment according to the existing literature and our own experience of long-term care for patients with eosinophilic granulomatosis with
Лакиза, Т.В. +5 more
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Eosinophilic Granulomatosis with Polyangiitis: The Beginning of a New Era [PDF]
, 2019 Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare type of anti-neutrophil cytoplasm antibody-associated vasculitis (AAV) with unique features, such as involvement of eosinophils in the pathogenesis, which requires different therapies from ...
Blanco, Marta Corral +2 more
core +1 more source
Clinical Case ReportsThis case highlights the atypical presentation of eosinophilic granulomatosis with polyangiitis (EGPA) with neurological and cardiac complications, emphasizing the necessity of early recognition and aggressive treatment to prevent morbidity and mortality.
Mahshid Talebi‐Taher +3 more
doaj +1 more source
Familial Eosinophilic Granulomatosis with Polyangiitis
Open Journal of Rheumatology and Autoimmune Diseases, 2017 Eosinophilic granulomatosis with polyangiitis (EGPA) is an uncommon ANCA associated vasculitic disorder characterized by systemic necrotizing vasculitis of small vessels occurring exclusively among patients with bronchial asthma and tissue eosinophilia. Familial EGPA is extremely rare. Only two case reports have been published so far.
Abdurhman S. Al Arfaj +4 more
openaire +2 more sources