Results 11 to 20 of about 117,766 (329)

Isolated Protein S Deficiency Presenting in Neonatal Inferior Vena Cava as Right Atrial Thrombus: A Case Report [PDF]

Indian Journal of Neonatal Medicine and Research, 2023
Critically ill neonates are at the greatest risk of developing thromboembolic disease. Multiple risk factors have been identified, one of which is isolated Protein S deficiency-a rare cause. The free form of Protein S plays a role in anticoagulation, and
Amritha Vinod, Karthikeyan Kadirvel, Amirtha Ganesh, V Premnath   +3 more
doaj   +1 more source

Aberrant Hematopoiesis and Morbidity in Extremely Preterm Infants With Intrauterine Growth Restriction

Frontiers in Pediatrics, 2021
Background and Objective: Intrauterine growth restriction (IUGR) poses additional challenges in extremely low gestational age newborns (ELGANs). We assessed disturbed hematopoiesis and morbidities associated with this disorder.Methods: This single-center
Nora J. Reibel, Christof Dame, Christoph Bührer, Tobias Muehlbacher, Tobias Muehlbacher   +4 more
doaj   +1 more source

The Coagulopathy-Predicting Factors In Acute Trauma Patients Using The Generalized Estimation Equations Model

Journal of Biostatistics and Epidemiology, 2022
Introduction: Coagulation disorder is one of the major phenomena following the trauma which can deteriorate the condition of the patients. The aim of this study is to determine some factors predicting the incidence of coagulation disorder among acute ...
Zahra Montazeri, Soleiman Kheiri, Shahram Paydar, Morteza Sedehi   +3 more
doaj   +1 more source

Coagulation and Mental Disorders [PDF]

Rambam Maimonides Medical Journal, 2014
The neurovascular unit is a key player in brain development, homeostasis, and pathology. Mental stress affects coagulation, while severe mental illnesses, such as recurrent depression and schizophrenia, are associated with an increased thrombotic risk and cardiovascular morbidity. Evidence indicates that the hemostatic system is involved to some extent
Hoirisch-Clapauch, Silvia, Nardi, Antonio Egidio, Gris, Jean-Christophe, Brenner, Benjamin   +3 more
openaire   +5 more sources

Congenital Hypofibrinogenemia: Presentation of a Rare Coagulation Disorder. [PDF]

Cureus, 2020
Acevedo Viales K, Valverde Muñoz K, Gutiérrez Valverde D.   +2 more
europepmc   +3 more sources

Precision medicine in hemostasis: a review of prothrombin complex concentrates and the role of viscoelastic tests in tailoring therapy

Emergency Care Journal, 2023
This review explores the role of precision medicine in the management of bleeding disorders and anticoagulation therapy, with a focus on the use of visco-elastic tests such as Thromboelastography (TEG) and Rotational Thromboelastometry (ROTEM).
Iacopo Cappellini, Franco Lai, Simone Magazzini, Guglielmo Consales   +3 more
doaj   +1 more source

Sex Differences in the Incidence and Risk Factors of Myocardial Injury in COVID-19 Patients: A Retrospective Cohort Study

Frontiers in Physiology, 2021
Male novel coronavirus disease (COVID-19) patients tend to have poorer clinical outcomes than female patients, while the myocardial injury is strongly associated with COVID-19-related adverse events.
Ran Cheng, Chuan Liu, Jie Yang, Yuanqi Yang, Renzheng Chen, Xiaohan Ding, Xiaohan Ding, Xubin Gao, Jingbin Ke, Fangzhengyuan Yuan, Chunyan He, Yang Shen, Limin Zhang, Limin Zhang, Ping Li, Ping Li, Hu Tan, Hu Tan, Lan Huang   +18 more
doaj   +1 more source

Predictive Model for Mortality in Severe COVID-19 Patients across the Six Pandemic Waves

Viruses, 2023
The impact of SARS-CoV-2 infection remains substantial on a global scale, despite widespread vaccination efforts, early therapeutic interventions, and an enhanced understanding of the disease’s underlying mechanisms.
Nazaret Casillas, Antonio Ramón, Ana María Torres, Pilar Blasco, Jorge Mateo   +4 more
doaj   +1 more source

A rare case of factor XIII deficiency presenting with scrotal hematoma in an adolescent

Indian Pediatrics Case Reports, 2021
Background: Factor XIII deficiency is a rare disorder that may be congenital or acquired and is considered if a coagulation disorder is suspected, but the initial laboratory investigations are normal.
Rajesh K Kulkarni, Sagar Vartak, Niharika Karandikar, Aarti Kinikar   +3 more
doaj   +1 more source

Mannose phosphate isomerase deficiency‐congenital disorder of glycosylation (MPI‐CDG) with cerebral venous sinus thrombosis as first and only presenting symptom: A rare but treatable cause of thrombophilia

JIMD Reports, 2020
Mannose phosphate isomerase deficiency‐congenital disorder of glycosylation (MPI‐CDG; formerly named CDG type 1b) is characterized by the clinical triad of hepatopathy, protein‐losing enteropathy, and hyperinsulinemic hypoglycemia in combination with ...
Chris Mühlhausen, Lisa Henneke, Lars Schlotawa, Daniel Behme, Marianne Grüneberg, Jutta Gärtner, Thorsten Marquardt   +6 more
doaj   +1 more source