Results 31 to 40 of about 2,453,026 (292)

Roughness effect on the correction factor of surface velocity for rill flows [PDF]

, 2021
Flow velocity is one of the most important hydrodynamic variables for both channelized (rill and gullies) and interrill erosive phenomena. The dye tracer technique to measure surface flow velocity Vs is based on the measurement of the travel time of a ...
Ferro V., Nicosia A., Palmeri V., Di Stefano C., Pampalone V.   +4 more
core   +1 more source

Warfarin-induced development of an acquired factor V inhibitor

Journal of Hospital General Medicine, 2023
Acquired factor V (FV) deficiency is characterized by bleeding tendency owing to the development of FV inhibitors. We encountered a case of this disease in a 90-year-old male patient who had been taking warfarin for more than 10 years.
Yuichi Sesumi, Yasushi Terada, Wataru Kaino, Toshihiro Yamagata, Shungo Nishimura   +4 more
doaj   +1 more source

Factor V Arg306 → Thr (factor V Cambridge) and factor V Arg306 → Gly mutations in venous thrombotic disease [PDF]

, 1998
We investigated the prevalence of two reported mutations of the factor V gene (factor V Arg306 → Thr, or factor V Cambridge, and factor V Arg306 → Gly) in 104 relatively young patients with verified venous thrombosis and in 208 age-, sex- and race ...
Maffei, Francisco Humberto de Abreu [UNESP], Lourenco, D., Maffei, Francisco Humberto de Abreu, Zago, M. A., Lourenco, Dayse Maria [UNIFESP], Thomazini, I. A. [UNESP], Thomazini, I. A., Morelli, Vania Maris [UNIFESP, Franco, R. F., Tavella, M. H., Thomazini, I. A [UNIFESP], Morelli, V., Piccinato, C. E., Maffei, Francisco Humberto de Abreu [UNIFESP]   +13 more
core   +1 more source

Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiency

Haematologica, 2008
We evaluated FV mRNA in severe factor V deficiency caused by the -12T/A IVS18 mutation, activating a cryptic splice site and leading to premature translation termination. Quantitative evaluation of factor V cDNA from homozygous and heterozygous subjects,
Barbara Lunghi, Mirko Pinotti, Iva Maestri, Angelika Batorova, Francesco Bernardi   +4 more
doaj   +1 more source

EPIDEMIOLOGY OF ACTIVATED PROTEIN C RESISTANCE AND FACTOR V LEIDEN MUTATION IN THE MEDITERRANEAN REGION

Mediterranean Journal of Hematology and Infectious Diseases, 2011
<!--[if gte mso 9]><xml> <o:OfficeDocumentSettings> <o:AllowPNG /> </o:OfficeDocumentSettings> </xml><![endif]--><!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <
Mehrez Mehrez M. Jadaon
doaj   +3 more sources

Hereditary combined deficiency of vitamin K–dependent clotting factors presenting as postoperative haemorrhage in a Syrian adolescent: a likely VKCFD type 2 phenotype

European Journal of Case Reports in Internal Medicine
Hereditary combined deficiency of vitamin K–dependent clotting factors (VKCFD) is a rare autosomal recessive disorder characterized by reduced activity of factors II, VII, IX, and X despite normal vitamin K levels.
Mahmoud Alhamadeh Alswij, Mais Musleh, Abdulhalim Mohamed Alyousef, Nizar Alsheekh Ahmad, Abdullatif AlStem, Hadi Ataya   +5 more
doaj   +1 more source

Prevalence of Factor V Leiden G1691A and Prothrombin G20210A Gene Mutation Among Pregnant Women: Experience from a Multi-Center Study in Nigeria

Journal of Blood Medicine, 2021
Sarah O John-Olabode,1 Kehinde S Okunade,2 Ayorinde James,3 Gbenga Olorunfemi,4 Obiefuna I Ajie,5 Akinniyi A Osuntoki,6 Alani S Akanmu1 1Department of Hematology and Blood Transfusion, College of Medicine, University of Lagos, Lagos, Nigeria; 2Department
John-Olabode SO, Okunade KS, James A, Olorunfemi G, Ajie OI, Osuntoki AA, Akanmu AS   +6 more
doaj  

Recurrent pregnancy loss: can factor V Leiden mutations be a cause [PDF]

Obstetrics & Gynecology Science, 2019
The role of Factor V Leiden (FVL) mutation in recurrent miscarriages has been disputed. It has been hypothesized that FVL mutation in patients with recurrent miscarriages is treatable.
R R N Reddy, Deepti Mutreja, Nikhil Moorchung, Indrayani Mukhopadhyay   +3 more
doaj   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen, Calogero Virgone, Antje Redlich, Michael Abele, Ricardo Lopez‐Almaraz, Tal Ben‐Ami, Ewa Bien, Gianni Bisogno, Maja Mazic Cesen, Andrea Ferrari, Malgorzata A. Krawczyk, Yves Reguerre, Dominik T. Schneider, Ines B. Brecht, Charlotte Rigaud, Bilgehan Yalcin, Rainer Claus, Christian Vokuhl, Constantin Lapa, Jörg Fuchs, Segolene Hescot, Thomas Walter, Julien Hadoux, Daniel Orbach   +23 more
wiley   +1 more source

Factor V Arg306->Gly Mutation Is Not Associated with Activated Protein C Resistance and Is Rare in Taiwanese Chinese [PDF]

, 2009
Polymerase chain reaction amplification followed by BstO1 enzyme digestion and DNA sequencing was employed to detect the mutation of factor V gene. The subjects consisted of 105 venous thrombophilic patients and 183 healthy controls. Only one patient was
沈銘鏡;林正修;蔡偉, SHEN, MING-CHING;LIN, JEN-SHIOU;TSAY, WOEI   +1 more
core