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Background: Alcohol use in autism spectrum disorder (ASD) is under-researched. Previous reviews have explored substance use as a whole, but this neglects individual characteristics unique to different substances. Alcohol use in non-clinical samples is associated with diverse responses.

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Chromogenic bacterial staining of teeth: a scoping review.

BMC Oral Health

January 2025

Basic Medical and Dental Sciences Department, College of Dentistry, Ajman University, Ajman, UAE.

Article Synopsis
  • This scoping review aims to investigate the causes, clinical traits, and treatment methods for chromogenic staining of teeth, following the PRISMA 2022 guidelines.
  • A systematic search across multiple medical databases led to the identification of 989 articles, with 21 ultimately included for analysis, highlighting that chromogenic bacteria can cause staining in 3.1 to 18.5% of cases, primarily resulting in black discoloration.
  • The findings indicate a lack of comprehensive literature on this topic, emphasizing the need for further research into effective management strategies for these challenging stains linked to specific oral bacteria.
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Over the past few decades, dental implants have been successfully utilized to replace teeth lost due to periodontal disease and other conditions. However, similar to natural teeth, dental implants are vulnerable to inflammatory peri-implant diseases, which can compromise their long-term viability. This review aims to summarize the current understanding of peri-implant diseases and discuss effective strategies for their diagnosis, treatment, and long-term management.

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Objective: To evaluate the relationship between infarct pattern, inferred stroke mechanism and risk of recurrence in patients with ischaemic stroke. The question is clinically relevant to optimise secondary stroke prevention investigations and treatment.

Design: We conducted a retrospective analysis of the dabigatran treatment of acute stroke II (DATAS II) trial (ClinicalTrials.

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Oligoasthenoteratozoospermia (OAT) is a frequent but severe type of male infertility. As one of the most multifaceted male infertility resulting from sperm problems, its genetic etiology remains unknown in most cases. In this review, we systematically sort out the latest literature on clinical reports and animal models leading to OAT, summarise the expression profiles of causative genes for OAT, and highlight the important role of the protein transport system during spermiogenesis, spermatid cell-specific genes, Golgi and acrosome-related genes, manchette-related genes, HTCA-related genes, and axoneme-related genes in OAT development.

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