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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11393660 | PMC |
| http://dx.doi.org/10.1002/emp2.13278 | DOI Listing |
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Heart failure of very rare aetiology-haemochromatosis Type 3: a case report.
Eur Heart J Case Rep
December 2024
Faculty of Medicine, Lithuanian University of Health Sciences, A. Mickevičiaus Str. 9, 44307 Kaunas, Lithuania.
Background: Haemochromatosis is a pathological condition characterized by the accumulation of iron in parenchymal organs, leading to toxic damage and dysfunction. Cardiac haemochromatosis represents one of the rare causes of severe heart failure (HF) that can be potentially prevented with targeted treatment.
Case Summary: We present the case of a 41-year-old female who was hospitalized for decompensated HF.
Application value of high-pressure-resistant peripherally inserted central catheters in enhanced computer tomography of diabetic patients with malignant tumors.
World J Diabetes
December 2024
Department of Radiology, The Second Affiliated Hospital, Jiangxi Medical College (Jiangxi Provincial Key Laboratory of Intelligent Medical Imaging), Nanchang University, Nanchang 330006, Jiangxi Province, China.
Background: Individuals with diabetes mellitus have a higher risk of developing malignant tumors, and diagnosing these tumors can be challenging.
Aim: To confirm the benefits of using peripherally inserted central catheters (PICCs) in contrast-enhanced computerized tomography (CECT) for diagnostic imaging in diabetic patients with malignant tumors and to provide a research basis for follow-up research.
Methods: This retrospective study analyzed 204 diabetic patients with malignancies treated at The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, from January 2024 to June 2024.
Spontaneous cerebrovascular reactivity at rest in older adults with and without mild cognitive impairment and memory deficits.
Alzheimers Dement
November 2024
Leonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Introduction: Older adults with mild cognitive impairment (MCI) exhibit deficits in cerebrovascular reactivity (CVR), suggesting CVR is a biomarker for vascular contributions to MCI. This study examined if spontaneous CVR is associated with MCI and memory impairment.
Methods: One hundred sixty-one older adults free of dementia or major neurological/psychiatric disorders were recruited.
Hereditary haemochromatosis: A review.
J R Coll Physicians Edinb
December 2024
Hepatology Department, York and Scarborough Teaching Hospitals NHS Foundation Trust.
Article Synopsis
- Hereditary haemochromatosis (HH) is a common genetic disorder in Northern Europeans, caused by mutations that lead to excessive iron absorption in the body, affecting various organs over time.
- Not everyone with the C282Y mutation develops HH, making early diagnosis crucial; however, most individuals may not show symptoms initially.
- Treatment typically involves venesection to reduce iron levels, which can alleviate symptoms and improve liver health, while those without mutations but showing liver iron overload may require further genetic testing.
Targeted Prostate Health Checks, a novel system to identify men with prostate cancer-A pilot study.
BJUI Compass
October 2024
Frimley Park Hospital, Frimley Health NHS Foundation Trust Frimley UK.
Objectives: The objective of this study is to report the pilot phase of the Targeted Prostate Health Check programme that aims to identify men in the Surrey and Sussex region who have prostate cancer and who failed to be detected during the Covid era.
Subjects And Methods: Men aged 50 to 70, or 45 to 70 if Black or with a family history of prostate cancer, were identified from participating general practitioner (GP) records. Short message service (SMS) texts invited men to visit www.
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