Results 91 to 100 of about 46,091 (305)
Allergy, EarlyView.ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas +128 more
wiley +1 more source
Classical autoimmune hepatitis and the IgG4-associated autoimmune hepatitis in paediatric patients
The IgG4-associated autoimmune hepatitis (IgG4-AIH) is a newly proposed disease entity characterised by the accumulation of the IgG4-expressing plasma cells in the liver. Its pathophysiology and clinical significance remain unclear and have poor evidence
Dorota Jarzębicka +6 more
core +1 more source
Characterization Of The Homologs Of A Diagnostically Significant Brugia Malayi Gene (Bm17DIII) In Wuchereria Bancrofti, Loa Loa and Onchocerca Volvulus [RA644.F5 R788 2007 f rb]. [PDF]
, 2006 Satu ujian pantas yang dikenali sebagai BRUGIArapid (BR) yang mengesan antibodi IgG4 terhadap antigen rekombinan B. malayi (BmR1) adalah sangat berguna dalam pemetaan dan pengawasan kawasan yang endemik bagi filariasis brugia.
Abdul Aziz, Ros Azeana
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Allergy, EarlyView.ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare and potentially life‐threatening systemic, inflammatory disease with multi‐organ manifestations, variable presentation and complex pathology. Multiple interconnected immunological pathways are implicated in EGPA pathology, including a type‐2 immune response driving predominantly ...
Harold Wilson‐Morkeh +7 more
wiley +1 more source
La maladie à IgG4: à propos de 3 cas
The Pan African Medical Journal, 2020 La maladie à IgG4 encore appelée polyexocrinopathie auto-immune à IgG4 est une nouvelle entité où s´inscrit la PAI de type 1. Elle peut toucher différents organes (système nerveux central, les glandes salivaires, la thyroïde, les poumons, le pancréas ...
Hakima Abid +11 more
doaj +1 more source
Topiramate-induced maculopathy in IgG4-related disease
, 2016 Joanna DaCosta,1,2 Saad Younis1 1Ophthalmology Department, Imperial College Healthcare NHS Trust, Western Eye Hospital, 2Barts Health NHS Trust, Whipps Cross University Hospital, London, UK Abstract: This report describes a case of reversible topiramate-
DaCosta J, Younis S
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Allergy, EarlyView.ABSTRACT In the last decades, critical advancements in research technology and knowledge on disease mechanisms steered therapeutic approaches for chronic inflammatory diseases towards unprecedented target specificity. For allergic and chronic lung diseases, biologic drugs pioneered this goal, acquiring on the way—through the clinical use of monoclonal ...
F. Roth‐Walter +20 more
wiley +1 more source
Serum total IgG and IgG4 levels in thyroid eye disease
, 2016 Aileen Sy, Rona Z Silkiss Department of Ophthalmology, California Pacific Medical Center, San Francisco, CA, USA Purpose: To investigate the relationship between immunoglobulin G (IgG)4-related disease (IgG4-RD) and thyroid eye disease (TED ...
Sy A, Silkiss RZ
core
, 2022 (1) Background: To analyze the association between long-term changes in serum IgG4 levels and the clinical course of patients with IgG4-related ophthalmic disease (IgG4-ROD). (2) Methods: Retrospective analysis of 25 patients with IgG4-ROD.
Ching-Yao Tsai +5 more
core +1 more source