Results 311 to 320 of about 448,079 (362)

Evaluation of Bleeding Phenotype of Inherited Factor VII Deficiency in Children With a Bleeding Assessment Tool and Global Assays

Journal of pediatric hematology/oncology, 2019
Introduction: Inherited factor VII (FVII) deficiency is the most common of the rare bleeding disorders and shows a heterogenous distribution of bleeding phenotypes independent of factor activity level.
Ersin Toret, Y. Ay, T. Karapınar, Y. Oymak, K. Kavaklı, R. Vergin   +5 more
semanticscholar   +1 more source

CONGENITAL DEFICIENCY OF FACTOR VII

Australasian Annals of Medicine, 1958
SummaryLaboratory investigations are described in a female patient who suffers from a congenital hæmorrhagic disorder due to deficiency of Factor VII. The one‐stage prothrombin time using brain extract was greatly prolonged, but using viper venom was normal. All tests of the intrinsic blood coagulation mechanism, including the thromboplastin generation
openaire   +3 more sources

Sensitivities of Thromboplastins to Factor VII Deficiency

American Journal of Clinical Pathology, 1971
Plasma from a factor VII deficient patient was used to compare the sensitivities of thromboplastins from different sources. The results based on time in seconds were compared with those in abnormal control plasmas. The factor VII deficiency was detected with all thromboplastins tested; however, some showed more “sensitivity” than others.
Ezra E. Kleiner, Lynn Heiges, Manabu Fukushima   +2 more
openaire   +3 more sources

Hereditary Factor‐VII Deficiency in the Beagle

British Journal of Haematology, 1972
Summary. Hereditary factor‐VII deficiency is identified in another large colony of beagles. Evidence is presented to suggest that this trait may be relatively widespread in colonies in Great Britain.
Linda K. Burton, T. Pilling, R. Peacock, N. W. Spurling   +3 more
openaire   +3 more sources

Case report of factor VII deficiency

The American Journal of Emergency Medicine, 1993
The case of a 57-year-old woman with no personal or family history of coagulopathy or blood dyscrasia who was found to be factor VII deficient by routine laboratory testing is reported. The patient was also found to have type 2 diabetes mellitus and adenocarcinoma of the uterus in the course of her hospitalization.
Curtis Harris, Robert L. Dupper, Alan J. Hirshberg, Ronald L. Fletcher   +3 more
openaire   +2 more sources

Unprovoked Pulmonary Embolism in Factor VII Deficiency

Acta Haematologica, 2019
Thrombotic events in bleeding disorders such as hemophilia A or B, Von Willebrand disease, afibrinogenemia, factor VII deficiency, and factor XI deficiency are rare but have been reported.
Balraj Singh, Varun Modi, Parminder Kaur, G. Guron, M. Maroules   +4 more
semanticscholar   +1 more source

Management of a patient with Factor VII deficiency

Oral Surgery, Oral Medicine, Oral Pathology, 1980
Several approaches to the dental treatment of patients with Factor VII deficiencies have been explained. The case of a patient with Factor VII deficiency who required dental extractions has been presented and the rationale for the treatment used in this case has been discussed.
James C. Perhavec, Jerold S. Goldberg
openaire   +3 more sources

Thromboembolism in Congenital Factor VII Deficiency

Acta Haematologica, 1984
An Israeli family of Persian origin was investigated for factor VII deficiency. The proposita, derived from a consanguineous marriage, had repeated thrombophlebitis attacks, pulmonary embolism and rectal bleeding. The family studied and the proposita had low factor VII procoagulant activity and low factor VII antigen.
I. Machtey, D. Creter, T. Shifter
openaire   +3 more sources

Hereditary Factor VII Deficiency in Newborns

Clinical Pediatrics, 1983
Chez 2 jumeaux monozygotes decedes d'hemorragie intracrânienne l'un a 3 mois, l'autre a 30 mois.
Robert Albers, Metin Bedizel
openaire   +3 more sources

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Thrombosis and Haemostasis, 2005
SummaryTo investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genotype, a multi-center study of factor VII (FVII) congenital deficiency with centralized genotyping and specific functional assays was carried out. FVII mutations characterized in patients (n=313) were extremely heterogeneous (103 different, 22 novel)
MARIANI G, HERRMANN FH, DOLCE A, BATOROVA A, ETRO, Daniela, PEYVANDI F, WULFF K, SCHVED JF, AUERSWALD G, INGERSLEV J, BERNARDI, Francesco, INTERNATIONAL FACTOR VII DEFICIENCY STUDY GROUP   +11 more
openaire   +6 more sources