Results 91 to 100 of about 98,834 (305)
PLoS ONE, 2020 Background Patients affected by angioedema due to hereditary and acquired C1-inhibitor (C1-INH) deficiency (HAE and AAE, respectively) report trouble accessing dental care, due to the risk of a life-threatening oropharyngeal and laryngeal attack ...
A. Zanichelli +8 more
semanticscholar +1 more source
Monocyte C1-Inhibitor Synthesis [PDF]
, 1987 C1-inhibitor is the major control protein of the classical pathway of complement. In man, its hereditary deficiency results in the clinical condition of hereditary angio-oedema (HAE).
Jones, Linda Margaret
core
Advanced Materials, EarlyView.Transition metal oxy/carbo‐nitrides show great promise as catalysts for sustainable processes. A Mn‐Mo mixed‐metal oxynitride attains remarkable performance for the direct synthesis of acetonitrile, an important commodity chemical, via sequential C─N and C─C coupling from syngas (C1) and ammonia (N1) feedstocks.
M. Elena Martínez‐Monje +7 more
wiley +1 more source
Romanian Journal of Laboratory Medicine, 2019 Background: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) caused by SERPING1 mutations is a rare monogenic disorder characterized by a high frequency of de novo mutations, allelic heterogeneity and populational differences.
Gábos Gabriella +7 more
doaj +1 more source
La Revue de medecine interne, 2020 Acquired angioedema with C1-inhibitor deficiency is a rare and peculiar entity belonging to the spectrum of bradykinin angioedemas. It usually occurs in subjects over 60 years old, and is mostly associated with a B-cell lymphoid hemopathy or a monoclonal
D. Gobert +13 more
semanticscholar +1 more source
Dexime: A Selectively Enzyme‐Degradable Hydrogel for Protein Therapeutic Release
Advanced Materials, EarlyView.A dextrin‐oxime hydrogel (dexime) is produced using ketone or aldehyde modified dextrin and tetra‐oxyamine modified poly(ethylene glycol). The rheological and mechanical properties of dexime are tunable. Dexime is injectable, cytocompatible, hydrolytically stable, and selectively degradable by α‐amylase.
Quinton E. A. Sirianni +5 more
wiley +1 more source
A Patient with Asymptomatic Connective Tissue Disease Coursing with Angioedema
İstanbul Medical Journal, 2017 Here we present the case of a patient who was diagnosed with non-familial angioedema (AE) and who had a high risk of connective tissue disease. The patient had recurrent AE and arthritis attacks. C1 inhibitor level was found to be borderline low, and the
Feridun Gürlek, Eyyüp Taşdemir
doaj +1 more source
Journal of Medical Case Reports, 2011 Introduction We report a rare, classic case of isolated angioedema of the bowel due to C1-esterase inhibitor deficiency. It is a rare presentation and very few cases have been reported worldwide. Angioedema has been classified into three categories. Case
Kothari Shivangi T +5 more
doaj +1 more source
Advanced Materials, EarlyView.A targeted modulation of the MoS2 electronic structure is achieved via substitutional n‐type Co/Fe co‐doping. This strategy triggers S‐mediated d‐p hybridization, optimizing the binding affinity with polysulfides to establish a volcano‐shaped relationship between the d‐band center and catalytic activity.
Junhyuk Ji +6 more
wiley +1 more source
Long-term prophylaxis therapy in patients with hereditary angioedema with C1 inhibitor deficiency.
Annals of Allergy, Asthma & Immunology, 2018 OBJECTIVE To review the criteria for long-term prophylaxis therapy in patients with hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE), describe how these criteria have evolved over time, and anticipate how criteria may change in the ...
T. Craig +8 more
semanticscholar +1 more source