Results 141 to 150 of about 22,562,840 (346)

Intracranial haemorrhage in a neonate with severe haemophilia A: A case report and literature review

open access: yesZdravniški Vestnik, 2012
Background: Intracranial haemorrhage (ICH) is a serious complication of haemophilia that affects 3.5–4 % of all boys with haemophilia during the neonatal period.
Barbara Faganel Kotnik   +5 more
doaj  

Recombinant B‐domain‐deleted porcine sequence factor VIII (r‐pFVIII) for the treatment of bleeding in patients with congenital haemophilia A and inhibitors

open access: yesHaemophilia, 2017
Development of inhibitors to human FVIII (hFVIII) significantly complicates the control of bleeding events in patients with haemophilia A.
Johnny Mahlangu   +4 more
semanticscholar   +1 more source

Endothelial cells derived from patients' induced pluripotent stem cells for sustained factor VIII delivery and the treatment of hemophilia A. [PDF]

open access: yes, 2020
Hemophilia A (HA) is a bleeding disorder characterized by spontaneous and prolonged hemorrhage. The disease is caused by mutations in the coagulation factor 8 gene (F8) leading to factor VIII (FVIII) deficiency.
Agu, Emmanuel   +9 more
core   +1 more source

Prenatal diagnosis for haemophilia: A nationwide survey among female carriers in the Netherlands [PDF]

open access: yes, 2011
Carriers of haemophilia face difficult choices regarding prenatal diagnosis, but little is known about the determinants that influence their decisions.
Balak, D.M.W. (Deepak)   +7 more
core   +2 more sources

Physical Activity Awareness and Understanding of Treatment Protection Among People With Haemophilia and Their Caregivers in Central Europe

open access: yesHaemophilia, EarlyView.
ABSTRACT Background Physical activity is now considered generally beneficial for persons with haemophilia (PWH). However, the specific type and extent of activity and its impact on quality of life (QoL) and bleed protection during exercise is under‐researched.
Angelika Batorova   +9 more
wiley   +1 more source

Clinical Features And Laboratory Patterns In A Cohort Of Consecutive Argentinian Patients With Von Willebrand's Disease [PDF]

open access: yes, 2001
Background and Objectives. von Willebrand's disease (vWD) is a bleeding disorder with variable clinical expression. Our aim was to classify patients with vWD and to determine the phenotype in their relatives. Design and Methods.
Blanco, A. N.   +6 more
core  

Endothelial cell processing and alternatively spliced transcripts of factor VIII: potential implications for coagulation cascades and pulmonary hypertension. [PDF]

open access: yes, 2010
BACKGROUND: Coagulation factor VIII (FVIII) deficiency leads to haemophilia A. Conversely, elevated plasma levels are a strong predictor of recurrent venous thromboemboli and pulmonary hypertension phenotypes in which in situ thromboses are implicated ...
Angus, G   +9 more
core   +1 more source

Severe haemophilia A with haemarthrosis improved on emicizumab: A case report

open access: yesThe Journal of Haemophilia Practice
Severe haemophilia A is associated with serious spontaneous bleeding in muscles, soft tissues, and joints. Haemarthrosis, bleeding into joints, is a serious complication of haemophilia. Emicizumab is a novel non-factor replacement agent for preventing or
Wasifuddin Mustafa, Al-Gaithi Ibrahim
doaj   +1 more source

Home - About - Disclaimer - Privacy