Publications by authors named "A l Beĭlin"

Introduction: Physiotherapists (PTs) working in primary care settings within an interprofessional team can lead to favourable health outcomes and decreased burden on the healthcare system. Although PT models of care are important to primary care delivery, there is a lack of knowledge and evidence on the characteristics of these models of care, the differences and similarities between the models, and the barriers and facilitators to implementing these models. This scoping review protocol aims to fill this knowledge gap by synthesizing the evidence and characteristics of models of care that integrate physiotherapists within primary care teams, mapping the similarities and differences, and describing barriers and facilitators to implementing models of care that integrate physiotherapists within primary care teams.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates outcome measures to assess physical functioning in patients undergoing lumbar spinal surgery, highlighting the importance of both patient-reported outcome measures (PROMs) and physical measures.
  • The research involves a systematic review with two stages: identifying relevant measures and assessing their measurement properties, conducted using multiple databases.
  • Results show that 1,101 reports were analyzed, identifying 70 established and 67 newly developed PROMs, along with 134 physical measures, with evidence supporting some measures' effectiveness, such as the 1-minute stair climb and 50-foot walk tests.
View Article and Find Full Text PDF

Immortalization (genetically induced prevention of replicative senescence) is a promising approach to obtain cellular material for cell therapy or for bio-artificial organs aimed at overcoming the problem of donor material shortage. Immortalization is reversed before cells are used in vivo to allow cell differentiation into the mature phenotype and avoid tumorigenic effects of unlimited cell proliferation. However, there is no certainty that the process of de-immortalization is 100% effective and that it does not cause unwanted changes in the cell.

View Article and Find Full Text PDF

Epidermolysis bullosa simplex (EBS) is a group of inherited keratinopathies that, in most cases, arise due to mutations in keratins and lead to intraepidermal ruptures. The cellular pathology of most EBS subtypes is associated with the fragility of the intermediate filament network, cytolysis of the basal layer of the epidermis, or attenuation of hemidesmosomal/desmosomal components. Mutations in keratins 5/14 or in other genes that encode associated proteins induce structural disarrangements of different strengths depending on their locations in the genes.

View Article and Find Full Text PDF