Results 91 to 100 of about 6,414 (212)
Blood Advances, 2017 : Routine testing for inherited and acquired thrombophilia defects is frequently performed in pediatric patients with thromboembolic events (TEEs). No consensus guidelines exist regarding the timing of testing or the type of patients to be tested.
Chakri Gavva +2 more
doaj +1 more source
Public Health Challenges, Volume 5, Issue 2, June 2026.Nearly half of ICU patients in Dhaka City are at high risk for venous thromboembolism by Padua risk assessment model, yet only 28.57% of high‐risk patients received prophylaxis. Mandatory systematic risk assessment and LMWH protocols are urgently needed to close this preventable care gap.
Md. Shek Sady Khan +10 more
wiley +1 more source
Laboratory detection of inherited thrombophilia: A historical perspective
, 2005 Considerable progress has been made in determining the molecular bases of inherited thrombophilia in the last 25 years. There are several genetic abnormalities that can be detected in the laboratory and are currently recognized to be unequivocally ...
P.M. Mannucci
core +1 more source
The study of normal pregnancy in women with hereditary thrombophilia
Акушерство, гинекология и репродукция, 2016 Objective: The definition of the conditions under which women with inherited thrombophilia can have a positive pregnancy outcome. Materials and Methods.
M. V. Khruslov +5 more
doaj +1 more source
AEG‐AESPANC‐OPGE‐SIED‐SPG Ibero‐Latin American Guidelines on Acute Pancreatitis (iLATAM‐AP)
United European Gastroenterology Journal, Volume 14, Issue 5, June 2026.ABSTRACT Introduction Acute pancreatitis (AP) is a major cause of gastrointestinal hospitalizations worldwide. Although typically self‐limiting, up to one‐third of cases develop complications associated with increased morbidity and mortality. Despite recent advances that have improved outcomes, clinical heterogeneity necessitates updated, evidence ...
Karina Cárdenas‐Jaén +44 more
wiley +1 more source
Clinical Utility of Stillbirth Investigations in Australia: A Cohort Study
Australian and New Zealand Journal of Obstetrics and Gynaecology, Volume 66, Issue 3, June 2026.ABSTRACT Background Stillbirths impact over two million parents globally every year. Despite current knowledge, technology, and investigations, many stillbirths remain unexplained and are not fully investigated. An important step forward in addressing this gap is determining which investigations produce the highest utility in identifying the cause of ...
Tania Marsden +22 more
wiley +1 more source
Bleeding, Thrombosis and Vascular BiologyBackground: The prevalence of thrombophilia in patients with unprovoked thrombotic events varies across populations, justifying the need for region-specific data to guide appropriate testing strategies.
Monisha Harimadhavan +7 more
doaj +1 more source
Adverse pregnancy outcomes and inherited thrombophilia
, 2017 Aim: (1) To evaluate the prevalence of inherited thrombophilia in pregnant women with adverse pregnancy outcomes: intrauterine growth retardation (IUGR), preeclampsia (PE) and placental abruption.
Dominik Dłuski +3 more
core +1 more source
Whole-exome sequencing in evaluation of patients with venous thromboembolism
Blood Advances, 2017 : Genetics play a significant role in venous thromboembolism (VTE), yet current clinical laboratory-based testing identifies a known heritable thrombophilia (factor V Leiden, prothrombin gene mutation G20210A, or a deficiency of protein C, protein S, or ...
Eun-Ju Lee +25 more
doaj +1 more source
Journal of Neurochemistry, Volume 170, Issue 6, June 2026.Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterised by progressive muscle weakness in both bulbar and extremity muscles, leading to a diverse clinical phenotype with motor and non‐motor symptoms. Cerebrospinal fluid (CSF) from sporadic ALS patients were analysed for proteomics content and revealed altered inflammatory and ...
Eleonora Sabetta +8 more
wiley +1 more source