Results 101 to 110 of about 83,381 (315)

Delivery of human apolipoprotein (apo) E to liver by an [E1(-), E3(-), polymerase(-), pTP(-)] adenovirus vector containing a liver-specific promoter inhibits atherogenesis in immunocompetent apoE-deficient mice [PDF]

open access: yes, 2006
Recombinant adenovirus (rAd)-mediated apoE gene transfer to the liver of apoE(-/-) mice is anti-atherogenic. However, first generation rAd vectors were associated with immune clearance of transduced hepatocytes, while an improved [E1(-), E3(-) polymerase(
Amalfitano, A   +4 more
core  

Acquired hemophilia A

open access: yesHematology, 2006
Acquired hemophilia A is a rare but severe autoimmune bleeding disorder, resulting from the presence of autoantibodies directed against clotting factor VIII. The etiology of the disorder remains obscure, although approximately half of all cases are associated with other underlying conditions.
openaire   +3 more sources

ORAL TREATMENT OF HEMOPHILIA [PDF]

open access: yes, 2007
Disclosed herein is a simple method for the treatment of antigen-deficiency diseases, by orally administering to a subject a therapeutically effective amount of the deficient antigen, wherein the antigen is not present in a liposome.
Alpan, Oral   +3 more
core   +1 more source

European Management of Glanzmann's Thrombasthenia: A Survey of Current Clinical Practice

open access: yesHaemophilia, EarlyView.
ABSTRACT Introduction Glanzmann's thrombasthenia is a rare inherited platelet disorder characterized by a lack of platelet aggregation. Patients tend to be diagnosed in early childhood with treatment strategies involving a multifaceted approach to prevent and manage bleeding episodes.
Mathieu Fiore   +6 more
wiley   +1 more source

Feasibility of Administering the Patient Reported Outcomes, Burdens and Experiences (PROBE) Questionnaire Through the Canadian Bleeding Disorders Registry (CBDR) and Comparison of Data From the Two Sources

open access: yesHaemophilia, EarlyView.
ABSTRACT Introduction The Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire can be used to measure quality of life in persons with haemophilia (PWH) and is integrated in the Canadian Bleeding Disorders Registry (CBDR). This offers the opportunity to compare the same data inputted by patients in PROBE and their treating team in ...
Federico Germini   +9 more
wiley   +1 more source

Hemophilia. [PDF]

open access: green, 1899
A. J. Cook
openalex   +1 more source

People With Haemophilia as Data Coordinators: An Analysis of the Ethics and Feasibility of Self‐Management With Personal Health Records

open access: yesHaemophilia, EarlyView.
ABSTRACT Background People with haemophilia perform various self‐management tasks, supported by multiple health apps. Personal health records will enable individuals to access and add health information from different institutions in a single digital tool, providing an integrated overview of data.
Martijn R. Brands   +6 more
wiley   +1 more source

Hemoaction game: an educational step to improve hemophilia children and nurses self-efficacy

open access: yesJournal of Advances in Medical Education and Professionalism, 2016
As hemophilia is a chronic bleeding disease and can interfere with daily performance of children, these children require continuous training to prevent bleeding and take timely action (1).
NOOASHIN BEHESHTIPOOR   +4 more
doaj  

Strontium Lactate in Hemophilia [PDF]

open access: green, 1907
NULL AUTHOR_ID
openalex   +1 more source

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