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Hemophilia A - Drug therapy
Research News and Information
Definition of 'Hemophilia A'The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. Common names: Hemophilia A; A, Hemophilia; As, Hemophilia; Hemophilia As; Haemophilia; Factor VIII Deficiency; Hemophilia; Deficiency, Factor VIII; Deficiencies, Factor VIII; Factor VIII Deficiencies |
Monday, November 23, 2009
2 Aug 2009
Recombinant FVIII formulated in PEG-ylated liposomes (rFVIII-PEG-Lip) was reported to increase the bleed-free days from 7 to 13 days (at 35 IU/kg rFVIII) in severe hemophilia A patients. To understand the underlying mechanism, we sought to ... Read more...
Multimerization of peptide mimotopes for blocking of factor VIII neutralizing antibodies.
30 Jul 2009
About 30 % of patients with severe hemophilia A develop neutralizing antibodies (inhibitors) to coagulation factor VIII (FVIII) upon treatment with exogenous factor preparations. Two peptides, C6 (NPVENMMDRDSQ) and H10 (QSPWQTWFTRAL), that mimic ... Read more...
30 Jul 2009
BACKGROUND: Postpartum hemorrhage may be a life-threatening event and may result from coagulation defects. CASE: We report a case of a multigravida woman who developed rapidly progressive postpartum bleeding as a result of acquired factor VIII ... Read more...
Latest indexed articles for 'Hemophilia A - Drug therapy'
These are the very latest articles for this heading:
- [89-year-old woman with hemorrhagic diathesis]
14 Sep 2009 - Enhanced efficacy of recombinant FVIII in noncovalent complex with PEGylated liposome in hemophilia A mice.
2 Aug 2009 - Multimerization of peptide mimotopes for blocking of factor VIII neutralizing antibodies.
30 Jul 2009 - A rapidly progressive, life-threatening postpartum hemorrhage: successful treatment with anti-CD-20 monoclonal antibody.
30 Jul 2009 - [Place of recombinant activated factor VII in the treatment of severe haemorrhage in paediatric patients]
29 Jun 2009 - The comparative immunogenicity of human and porcine factor VIII in haemophilia A mice.
29 Jun 2009 - Lineages of human T-cell clones, including T helper 17/T helper 1 cells, isolated at different stages of anti-factor VIII immune responses.
21 Jun 2009 - Factor VIII-von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII-von Willebrand factor interactions.
6 Jun 2009 - Successful treatment with rituximab in an elderly patient with acquired factor VIII inhibitor.
30 May 2009 - Therapeutic properties and safety of recombinant factor VIII and factor IX.
30 May 2009 - Intensive peri-operative use of factor VIII and the Arg593-->Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A.
30 May 2009 - Acquired hemophilia A with sigmoid colon cancer: successful treatment with rituximab followed by sigmoidectomy.
28 May 2009 - Recombinant and plasma-derived factor VIII products induce distinct splenic cytokine microenvironments in hemophilia A mice.
29 Apr 2009 - Quantifying the source of infection for HIV-infected hemophiliacs in the U.K. from 1979 to 1984.
29 Apr 2009 - [Relevance of a single dose of 270 microg/kg recombinant factor VIIa for the treatment of patients with haemophilia and inhibitors - Recommendations from the GTH experts]
29 Apr 2009 - Inhibitor treatment by rituximab in congenital haemophilia A - Two case reports.
29 Apr 2009 - Spontaneous disappearance of high titre factor VIII inhibitor 15 years after unsuccessful ITI.
29 Apr 2009 - Bacterial endocarditis and septic arthritis in a patient with severe hemophilia A: a case report.
29 Apr 2009 - The role of tissue factor and factor VIIa in hemostasis.
29 Apr 2009 - Characterization of a novel mutation in the F8 promoter region associated with mild hemophilia A and resistance to DDAVP therapy.
28 Apr 2009
See a longer list of these articles.
Technical information about 'Hemophilia A'
Definition: The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
Descriptor UI: D006467
Alternative terms: Hemophilia A; A, Hemophilia; As, Hemophilia; Hemophilia As; Haemophilia; Factor VIII Deficiency; Hemophilia; Deficiency, Factor VIII; Deficiencies, Factor VIII; Factor VIII Deficiencies;
Related Mesh Headings: Hemophilia B; Hemarthrosis;
Allowable Qualifiers: blood; cerebrospinal fluid; chemically induced; classification; complications; diagnosis; diet therapy; drug therapy; economics; embryology; enzymology; ethnology; etiology; genetics; history; immunology; metabolism; microbiology; mortality; nursing; epidemiology; parasitology; pathology; physiopathology; prevention & control; psychology; radiography; radionuclide imaging; radiotherapy; rehabilitation; surgery; therapy; urine; veterinary; ultrasonography; virology;
Tree Number: C15.378.100.100.500; C15.378.100.141.500; C15.378.463.500; C16.320.099.500;
History Note: 99(66)