Results 211 to 220 of about 32,190 (255)

LIVER TRANSPLANTATION FOR FACTOR VII DEFICIENCY

Transplantation, 2001
Factor VII deficiency is a serious, potentially lethal disorder of blood coagulation caused by a defect in hepatic factor VII synthesis. We report two children, sisters, both with severe, recurrent hemorrhagic complications from factor VII deficiency, successfully treated with orthotopic liver transplantation.
D, Levi, A, Pefkarou, J A, Fort, W, DeFaria, A G, Tzakis   +4 more
openaire   +2 more sources

Hobby-Induced Factor VII Deficiency

Pathophysiology of Haemostasis and Thrombosis, 2009
Hemorrhagíc tendency and granulocytopenia due to prolonged contact with trichloroethylene and toluene are described in a boy whose hobby was model air-plane assembly. The hemostatic defects found were hypoproconvertinemia, moderate hypofibrinogenemia, and increased capillary fragility.
J, Pinkhas, I, Cohen, J, Kruglak, A, de Vries   +3 more
openaire   +2 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.
A J, Hirshberg, R L, Fletcher, C, Harris, R L, Dupper   +3 more
openaire   +2 more sources

Factor VII Deficiency

2018
This chapter outlines the pathophysiology, clinical presentation, inheritance, and incidence of factor VII deficiency. The chapter describes the interaction with pregnancy and discusses the medical and anesthetic management of pregnant women with factor VII deficiency, including treatment of acute hemorrhage.
James P. R. Brown, Joanne Douglas
openaire   +1 more source

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.
N W, Spurling, L K, Burton, R, Peacock, T, Pilling   +3 more
openaire   +2 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.
M, Bedizel, R, Albers
openaire   +2 more sources

Thromboembolism in Congenital Factor VII Deficiency

Acta Haematologica, 2009
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.
T, Shifter, I, Machtey, D, Creter
openaire   +2 more sources

Factor VII deficiency and its treatment in delivery with recombinant factor VII

European Journal of Obstetrics, Gynecology and Reproductive Biology, 2004
The authors present two cases of pregnant women with coagulation disorders--one with inherited deficiency of factor VII and the second with chronic hepatitis. Both cases were successfully treated with recombinant activated factor VII of coagulation (NovoSeven) in delivery. The advantages of using this product are discussed.
B, Pehlivanov, N, Milchev, G, Kroumov
exaly   +3 more sources

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.
J C, Perhavec, J S, Goldberg
openaire   +2 more sources

Active and Inactive Factor VII in Dubin‐Johnson Syndrome with Factor‐VII Deficiency, Hereditary Factor‐VII Deficiency and on Coumadin Administration

British Journal of Haematology, 1972
Summary. Factor VII was purified from a lyophilized powder of PTC complex (Hemoplex, Cutter Laboratories) and an antiserum was prepared in rabbits to the partially‐purified fraction. The antiserum was found to inhibit specifically factor VII of normal plasma and the activity of the purified factor‐VII preparation.Inactive factor‐VII‐like material was ...
M, Levanon, S, Rimon, M, Shani, B, Ramot, E, Goldberg   +4 more
openaire   +2 more sources