Results 161 to 170 of about 9,507,633 (348)
Bioethics, EarlyView.ABSTRACT Recent literature has seen a growing endorsement of the so‐called autonomy‐only approach to assisted dying, which rejects suffering as a necessary criterion for access. Proponents argue that this model is most suitable to safeguard individuals against value‐based judgments of healthcare professionals about whether their lives are still worth ...
Meike Gerber
wiley +1 more source
Quantifying the impact of the COVID-19 pandemic on invasive bacterial diseases across 27 countries and territories: prospective surveillance by the IRIS Consortium [PDF]
David Shaw +99 more
openalex +1 more source
Malarial Diseases of the Cornea and Iris [PDF]
The American Journal of the Medical Sciences, 1901 openaire +1 more source
Severe non-specific immune reconstitution inflammatory syndrome (IRIS) presenting with graft-versus-host disease-like colitis [PDF]
, 2014 Simone Reu, Jens Neumann, Rika Draenert
openalex +1 more source
Fluoride Varnish for Caries Prevention in Preschoolers: An Overview of Reviews
Community Dentistry and Oral Epidemiology, EarlyView.ABSTRACT Objectives This study aimed to overview the available evidence from systematic reviews (SRs) on the effects of fluoride varnish (FV) for caries prevention in preschoolers. Methods Systematic reviews, with or without meta‐analyses, of randomised controlled trials (RCTs) and quasi‐randomised trials evaluating the use of FV in preschoolers to ...
Flávia Macedo Couto +5 more
wiley +1 more source
Prevalence and Associated Factors for Thyroid Eye Disease (TED) in the AAO IRIS® Registry
, 2020 Leslie Hyman +7 more
openalex +1 more source
Clinical Genetics, EarlyView.A novel CPAMD8 nonsense mutation c.2679C>G (p.Tyr893*) was identified in a patient with congenital microcoria, leading to reduced mRNA expression and predicted protein truncation. ABSTRACT Congenital microcoria (MCOR) is a rare inherited ocular disorder. Here, we describe a novel nonsense variant in the CPAMD8 gene in a patient with MCOR.
Jing‐Fan Gao +4 more
wiley +1 more source
The Phenotypic and Genotypic Features of ADAMTSL4‐Related Ocular Disease
Clinical Genetics, EarlyView.ADAMTSL4‐related ocular disease tends to present at a younger age and be associated with higher myopia than other forms of ectopia lentis (such as FBN1). A previously reported 20‐bp deletion (c.767_786del) was highly prevalent in this cohort (23/32), and all ectopia lentis et pupillae cases carried this variant. ABSTRACT Pathogenic variants in ADAMTSL4
Katie M. Williams +14 more
wiley +1 more source