Results 221 to 230 of about 92,991 (335)
The value of DHR-enzyme-linked immunosorbent assay in the diagnosis of chronic granulomatous disease by detecting NADPH oxidase complex activity. [PDF]
Xiaohui W +8 more
europepmc +1 more source
The Changing Paradigm of Management of Liver Abscesses in Chronic Granulomatous Disease [PDF]
David M. Straughan +19 more
openalex +1 more source
A 66‐year‐old man with acute retinal necrosis
Brain Pathology, EarlyView.
Shino Magaki +3 more
wiley +1 more source
Irreversible ECM proteolysis by remodeling enzymes shapes development, homeostasis, and disease. ECM‐degrading proteases display cell specificity and are governed by shared mechanisms, exhibiting functional redundancy in generating matrikines, growth factors, and cytokines.
Inna Solomonov, Orit Kollet, Irit Sagi
wiley +1 more source
Reliable genetic diagnosis of <i>NCF1</i> (p47<sup>phox</sup>)-deficient chronic granulomatous disease using high-throughput sequencing. [PDF]
Hsu AP +13 more
europepmc +1 more source
Clinical presentation, diagnostic findings and long-term survival in large breed dogs with meningoencephalitis of unknown aetiology [PDF]
ADAMO +28 more
core +1 more source
ABSTRACT Aim To evaluate the impact of polymorphisms in SOCS‐1, TNF‐α and RANKL on gene expression of RANK, RANKL, TNFRSF1, SOCS‐1, IL‐10, IL‐1β and TNF‐α, and to evaluate the histopathological, immunohistochemical and microbiological aspects of persistent apical periodontitis (PAP) after root canal treatment (RCT) in Brazilian individuals ...
Igor Bassi Ferreira Petean +12 more
wiley +1 more source
Diagnosing Systemic Mastocytosis: State of the Art
ABSTRACT With the advent of effective multikinase and selective tyrosine kinase inhibitors in systemic mastocytosis, diagnosing this rare disease has been critical to improving patient morbidity and mortality. This state‐of‐the‐art review interprets the international diagnostic criteria, including differences between the WHO 5th edition classification ...
Anton Rets, Tracy I. George
wiley +1 more source
Severe clinical phenotypes of heterozygous females with X-linked chronic granulomatous disease. [PDF]
Patel NC +9 more
europepmc +1 more source

