Results 21 to 30 of about 13,721,448 (320)

DIEP reconstruction in a patient with Factor V Leiden deficiency: A case report and literature review. [PDF]

JPRAS Open
Quinn O, Bhatti S, Rosich-Medina A.
europepmc   +3 more sources

Factor V Leiden Mutation and Neonatal Stroke

Pediatric Neurology Briefs, 1997
Three infants with familial factor V Leiden mutation and neonatal cerebrovascular disorders are reported from the Children’s Hospital of Philadelphia, PA.
J Gordon Millichap
doaj   +2 more sources

Prothrombin G20210A and Factor V Leiden Variants Are Not Associated With Thrombotic Events in Congenital Heart Disease: An Observational Trial. [PDF]

J Am Heart Assoc
Ladha FA, VanderPluym C, Mondragon-Estrada E, Avillach P, Brueckner M, Chung WK, Cnota JF, Gelb BD, Lewis M, Liu C, Roberts AE, Seidman CE, Tristani-Firouzi M, Wagner M, Morton SU, Newburger JW, Pediatric Cardiac Genomics Consortium Investigators.   +16 more
europepmc   +2 more sources

Fator V de Leiden Factor V Leiden

Revista Brasileira de Hematologia e Hemoterapia, 2005
José M. P. Godoy
doaj   +2 more sources

Acute graft thrombosis in a patient with factor V Leiden mutation: A case report and review of literature. [PDF]

World J Transplant
Lekehal B, Ait Youssef N, Lekehal M, Jdar A, El Hassani AEA, Belyazid I, Bakkali T, Bounssir A.   +7 more
europepmc   +3 more sources

The prevalence of Factor V Leiden (Arg506Gln) mutation in King Khalid University Hospital patients, 2017–2019 [PDF]

, 2021
Arg506Gln mutation is responsible for one of the procoagulant factors and most common inherited thrombophilia in the Factor V Leiden (FVL) family. The replacement of the missense mutation for Arg506Gln / R506Q is at 1691st position from Guanine to ...
Alotaibi, Abdulaziz A., AlEnezy, Reema Bader, Althnayan, Rahaf, Alhadlg, Munira Abdulrahman, Alayed, Nada, Al-Otaiby, Maram, AlQahtani, Sara H, Ghufran, Noman, Binmethem, Alanoud, Alaqeel, Arjuwana, Ali Khan, Imran   +10 more
core   +1 more source

A Rare Case of Quadruple Limb Amputation due to Factor V Leiden Mutation

Indian Journal of Physical Medicine & Rehabilitation, 2022
Factor V Leiden, an autosomal dominant gene mutation that leads to increase risk of forming thrombophilia. Amputation in patients with Factor V leiden mutation is known but none describe quad-limb amputation in this setting.
Ann Noble Zachariah, Ravi Sankaran
doaj   +1 more source

Left Renal Artery Thrombosis in a Patient With von Willebrand Disease Type 3 and Factor V Leiden Heterozygosity. [PDF]

Cureus
Albright NL, Kamboj S, Lucas JM.
europepmc   +3 more sources

Factor V Leiden and Inflammation [PDF]

Thrombosis, 2012
Factor V Leiden, is a variant of human factor V (FV), also known as proaccelerin, which leads to a hypercoagulable state. Along these years, factor V Leiden (FVL) has been studied from the pathophysiologic point of view, and research has been focused on finding clinical approaches for the management of the FVL associated to a trombophilic state.
Silvia Perez-Pujol, Omer Aras, Gines Escolar   +2 more
openaire   +2 more sources

Factor V Leiden [PDF]

The Journal of Perinatal & Neonatal Nursing, 2003
Factor V Leiden, formed by a genetic mutation, disrupts the body's anticoagulation defense system. It was isolated as recently as 1994 as a risk factor for venous thromboembolism. Factor V Leiden has also been linked to preeclampsia, pregnancy loss, and fetal growth restriction.
Deborah L. Ornstein, Mary Cushman
openaire   +3 more sources