Results 71 to 80 of about 49,732 (222)

A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus

open access: yes, 2015
Immunoglobulin (Ig) G4-related systemic syndrome is a recently described entity characterized by elevated serum IgG4 and tissue infiltration of IgG4-positive plasma cells. Pituitary gland can be involved as hypophysitis. We report a case of a 72-year-old
Yumi Harano   +4 more
core   +1 more source

IgG4-related autoimmune liver disease

open access: yes, 2023
The term IgG4-related autoimmune liver disease (AILD) refers to hepato-biliary manifestations of Immunoglobin G4-related disease (IgG4-RD) including IgG4-related sclerosing cholangitis and IgG4-related pseudotumor.
Pedica F.   +3 more
core   +1 more source

Analysis of Carbohydrates and Glycoconjugates by Matrix‐Assisted Laser Desorption/Ionization Mass Spectrometry: An Update for 2023–2024

open access: yesMass Spectrometry Reviews, EarlyView.
ABSTRACT The use of MALDI mass spectrometry for the analysis of carbohydrates and glycoconjugates is a well‐established technique and this comprehensive review is the twelfth update of the original article published in 1999 and brings coverage of the literature to the end of 2024.
David J. Harvey
wiley   +1 more source

IgG4-Related Disease Involving the Ear: A Case Report [PDF]

open access: yes
IgG4-related disease is a chronic inflammatory disease with widespread clinical presentation. It mimics various malignant, infectious, and inflammatory conditions, leading to confusion in diagnosis and management.
Ushant Acharya   +2 more
core   +1 more source

IgG4-related disease in the head and neck region: report of two cases and review of the literature [PDF]

open access: yes, 2016
IgG4-related disease (IgG4-RD) is a rare immune-mediated condition characterized by extensive tissue fibrosis and infiltration by immunoglobulin G4 positive plasma cells in a single organ or systemic appearance.
Jan Zapała   +11 more
core   +1 more source

Targeting the CD47–SIRPα phagocytic checkpoint in cancer: Biology, translational opportunities, and next‐generation therapeutic strategies

open access: yesSmart Molecules, EarlyView.
The CD47–SIRPα axis has emerged as a critical innate immune checkpoint that suppresses macrophage‐mediated phagocytosis through a canonical “don't eat me” signal and enables tumor immune evasion. We comprehensively summarize the structural and biological features of CD47 and the molecular mechanisms underlying CD47‐mediated regulation of phagocytosis ...
Ruimei Zhou   +4 more
wiley   +1 more source

IgG4 autoantibodies and autoantigens in the context of IgG4-autoimmune disease and IgG4-related disease [PDF]

open access: yes
Immunoglobulins are an essential part of the humoral immune response. IgG4 antibodies are the least prevalent subclass and have unique structural and functional properties. In this review, we discuss IgG4 class switch and B cell production. We review the
Emma L. Culver, Rodrigo V. Motta
core   +3 more sources

IgG4-positive Plasmocytosis of Inflammatory Cell Spreading Pattern Revealed to Differentiation in Classic Oral Lichen Planus [PDF]

open access: yes, 2013
Objective:Oral lichen planus( OLP) is a chronic inflammatory oral mucosal disease of unknown etiology.Due to similar histological features of OLP with other oral diseases.
Imai, Yutaka   +7 more
core  

Eosinophilic Sialodochitis Identified in Duct Remnant After Submandibular Gland Resection

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Eosinophilic sialodochitis (ES) is an increasingly recognized cause of recurrent sialadenitis but likely remains underdiagnosed as it is commonly considered to be nonspecific chronic sialadenitis. ES is likely increasing in prevalence in association with the growing number of allergic diseases and should be considered in patients presenting ...
Edward Tannenbaum   +3 more
wiley   +1 more source

Sjögren’s syndrome versus IgG4-related diseases – classification difficulties and treatment progress

open access: yes, 2014
Sjögren’s syndrome (SS) is a chronic autoimmune disorder characterized by lymphocytic infiltration in exocrine glands mainly salivary and lacrimal which affects impairment of their functions.
Jacek Falkowski, Anna Nowakowska-Płaza
core   +1 more source

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