Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Tracheobronchial injury after blunt thoracic trauma-lessons to learn in diagnosis, treatment, and postoperative care: a case series.
J Thorac Dis
September 2024
Section of Thoracic Surgery, Department of Visceral-, Transplant-, Thoracic and Vascular Surgery, University Hospital Leipzig, Leipzig, Germany.
Background: Tracheobronchial injury (TBI) is the subsuming term to describe rare and mostly traumatic damage to the tracheobronchial tree. Prehospital mortality is significant. TBI patients may face delayed diagnosis, challenging perioperative care, and prolonged recovery.
View Article and Find Full Text PDFOn human-in-the-loop optimization of human-robot interaction.
Nature
September 2024
Department of Mechanical Engineering, Stanford University, Stanford, CA, USA.
Article Synopsis
- Robots that closely interact with people, like exoskeletons and medical devices, are set to improve our lives significantly, but their design is challenging due to human complexity and unpredictable responses.
- A new strategy called human-in-the-loop optimization helps overcome these challenges by tailoring device features to enhance user performance based on specific needs and contexts.
- This approach not only improves human-robot collaboration in research but also presents opportunities for developing new optimization techniques, ultimately aiming to create devices that better the human experience.
Co-Occurrence of Myotonic Dystrophy Type 1 and Limb-Girdle Muscular Dystrophy Type 2B: A Case Report.
Mol Syndromol
February 2024
Medical Genetics Service, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil.
Article Synopsis
- Myotonic dystrophy type 1 (DM1) is a dominant neuromuscular disease with distal weakness, while limb-girdle muscular dystrophy type 2B (LGMD2B) is a recessive condition characterized by proximal weakness, which may coexist in patients with a family history of consanguinity.
- A reported case involves a 38-year-old woman diagnosed with both DM1 and LGMD2B, highlighting that genetic testing revealed the LGMD2B diagnosis due to her consanguineous parents and elevated creatine kinase levels.
- Identifying atypical disease presentations is crucial, as it may indicate the presence of a second genetic disorder, leading to improved genetic counseling and appropriate treatment options.
Myotonic dystrophy type 1 (Steinert disease): 29 years of experience at a tertiary pediatric hospital.
Eur J Paediatr Neurol
January 2024
Multidisciplinary Pediatric Neuromuscular Diseases Team, CMIN, CHUdSA, European Reference Network for Rare Neuromuscular Diseases (EURO-NMD) Center, Porto, Portugal.
Background: Myotonic dystrophy type 1 (DM1) is a multisystemic disorder caused by the expansion of a noncoding triplet repeat.
Methods: A cross-sectional study was performed to characterize pediatric patients with DM1 followed in a tertiary hospital over the last 29 years, comparing the congenital and the childhood/juvenile-onset forms.
Results: Thirty-seven patients (59.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!