Results 71 to 80 of about 1,143,701 (190)
Pathophysiological aspects of Gilbert's syndrome and Crigler-Najjar syndrome type II [PDF]
To determine the common pathophysiological basis in Gilbert's syndrome and Crigler-Najjar syndrome type II, biliary bilirubin moieties and hepatic bilirubin UDP-glucuronosyltransferase activity were measured.
Yamamoto, Toshio +5 more
core
Abstract Tourette syndrome [TS] is a neurological disorder of childhood onset characterised by the occurrence of tics: repetitive, purposeless movements or vocalisations. Effective treatment for tic disorders is an area of considerable unmet clinical need.
Stephen R. Jackson +2 more
wiley +1 more source
Prevalence of suspected Gilbert’s syndrome in Golestan province, northern Iran (2014)
Background and Objective: Gilbertchr('39')s syndrome is a relatively common genetic disorder, which is caused by defection in uridine diphosphate glucuronosyl transferase enzyme. The indirect bilirubin increases in this syndrome, although the function of
Azadeh Aliarab +7 more
doaj
The (trans)national Russian religious imagination in exile: Iulia de Beausobre (1893‐1977)
Abstract The article offers a case study of how Russian Orthodox who migrated from the Soviet Union after the Bolshevik Revolution of 1917 reimagined their religious identity and their church in a transnational setting. Iulia de Beausobre (1893‐1977) was a Russian aristocrat who fell victim to the Stalinist purges but survived the Soviet prison system ...
Ruth Coates
wiley +1 more source
The unusual clinical presentation of leptospirosis is masked by Gilbert’s syndrome
Leptospirosis is a zoonotic disease endemic to tropical regions, with flu-like symptoms that make early diagnosis difficult. This study describes the case of a 23-year-old man with a history of Gilbert’s syndrome and mixed anxiety and depressive disorder
Liliana Sánchez-Lerma
doaj +1 more source
Hyperbilirubinemia following lenalidomide administration
Key Clinical Message Asymptomatic hyperbilirubinemia in a patient with no underlying liver disease or renal impairment while on lenalidomide therapy may be attributable to the unmasking of previously undiagnosed Gilbert's syndrome, as previously shown in
Veronica Azmy, Natalia Neparidze
doaj +1 more source
Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort [PDF]
BACKGROUND & AIMS: Bilirubin has potent antioxidant properties in vitro and raised serum levels have been associated with lower rates of respiratory disease.
Swallow, DM +9 more
core +1 more source
ABSTRACT Objective To evaluate salivary apelin levels in individuals with and without type 1 diabetes presenting an intact periodontium and varying degrees of plaque‐induced gingival inflammation. Methods Saliva samples were collected; and whole‐mouth clinical periodontal measurements were recorded in type 1 diabetes and systemically healthy ...
Demet Efe Yavaşoğlu +6 more
wiley +1 more source
ABSTRACT Objective To assess the association between mechanical power (MP) and survival in mechanically ventilated dogs with primary pulmonary parenchymal disease and to compare its prognostic performance against individual ventilator parameters and oxygenation indices. Design Retrospective, multicenter observational cohort study.
Tereza Stastny +7 more
wiley +1 more source
Multiscale four‐dimensional imaging of cardiac remodelling after myocardial infarction
Abstract figure legend Multiscale 4D imaging framework for integrated phenotyping of post‐infarction remodelling. Myocardial infarction triggers dynamic changes across mechanical, haemodynamic and biological axes, progressing from acute injury and inflammation to extracellular matrix remodelling and scar maturation.
Hanzhou Lei, Boris Martinac, Yang Guo
wiley +1 more source

