Results 221 to 230 of about 32,190 (255)

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
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Combined Factor VII and Factor VIII Deficiency Due to a Casual Association of Heterozygosis for Factor VII Deficiency and Hemophilia A

Acta Haematologica, 2009
A patient with combined factor VII and factor VIII deficiency is discussed. The propositus is a 21-year-old male who presented a mild bleeding tendency. The patient appears to be a hemophilia and at the same time heterozygote for factor VII deficiency. This conclusion is based on the fact that heterozygosis for factor VII deficiency was present in the ...
Girolami A, Dal Bo Zanon R, FABRIS, FABRIZIO, Franzoso R.   +3 more
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Factor VII deficiency and cardiac surgery

European Journal of Anaesthesiology, 2004
info:eu-repo/semantics ...
Tuna, Turgay, Massaut, Jacques, Wauthy, Pierre, Beckers, Stefan   +3 more
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An overview of inherited factor VII deficiency

Transfusion and Apheresis Science, 2019
Factor VII (FVII) deficiency is the most common of the Rare Inherited Coagulation Disorders. The inheritance is autosomal recessive but there is variable penetrance. Overall there is poor correlation between the FVII level and the bleeding phenotype. Heterozygotes may have significant bleeding and severe homozygotes, or compound heterozygotes can be ...
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Congenital Factor VII Deficiency

2018
Coagulation factor (F) II (prothrombin) is a vitamin K-dependent coagulation factor which has an essential role in coagulation cascade. This protein is activated to thrombin by Factor X in the presence of FV and calcium. Congenital FII deficiency is an autosomal recessive bleeding disorder with an estimated incidence of 1:2,000,000 worldwide.
Mahmood Shams, Akbar Dorgalaleh
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Canine Factor‐VII Deficiency

British Journal of Haematology, 1962
J F, MUSTARD, D, SECORD, T D, HOEKSEMA, H G, DOWNIE, H C, ROWSELL   +4 more
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Open heart surgery with factor VII deficiency.

The Journal of cardiovascular surgery, 1983
A case with marked factor VII deficiency, undergoing open heart surgery for atrial myxoma, is reported. The syndrome was unknown to the patient and only pre-operative routine coagulation studies showed a low prothrombin activity (22%). Further investigations revealed a severe factor VII deficiency.
Gagliardi C, D'Avino R, Stassano P, Musumeci A, Spampinato N   +4 more
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Factor VII Deficiency

The Biomedical & Life Sciences Collection
Anskar Y.H. Leung, Edmond S.K. Ma
  +4 more sources

[Factor VII deficiency and surgery].

Annales francaises d'anesthesie et de reanimation, 1999
Factor VII deficiency is a rare disorder (1/500,000), with manifestations similar to those experienced by patients with haemophilia. Excessive bleeding during surgical procedure is prevented by factor VII administration. We report two cases of patients presenting a factor VII deficiency who were treated for oncological surgery.
J Y, Ranchère, C, Ménart, A, Lienhart, O, Attali   +3 more
openaire   +1 more source

Factor VII deficiency in an Alaskan Malamute

Australian Veterinary Journal, 1997
Mills, J.N., Labuc, R.H., Lawley, M.J.
openaire   +2 more sources