Results 181 to 190 of about 212,775 (379)

Increased von Willebrand Factor and Defective Ristocetin-Induced platelet Aggregation in Liver Disease [PDF]

, 1977
S Maragall, Antonio Ordinas, Carmine Clemente, F Casals, J. Profitós, R. Castillo   +5 more
openalex   +1 more source

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

Haemophilia, 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, Atanas Banchev, Ana Boban, Brigitte Brand, Melen Brinza, Barbara Faganel Kotnik, Csongor Kiss, Gediminas Puras, Jan Rajnoch, Ester Zapotocka   +9 more
wiley   +1 more source

Decreased plasma ADAMTS-13 activity as a predictor of postoperative bleeding in cyanotic congenital heart disease

Clinics, 2013
OBJECTIVE: To analyze the preoperative plasma antigenic concentration and activity of von Willebrand factor and its main cleaving protease ADAMTS-13 in pediatric patients with cyanotic congenital heart disease undergoing surgical treatment and ...
Rosangela P.S. Soares, Sérgio P. Bydlowski, Marcelo B. Jatene, Janete Ferreira Hironaka, Antonio Augusto Lopes   +4 more
doaj  

von Willebrand factor. [PDF]

Journal of Biological Chemistry, 1991
openaire   +2 more sources

European Principles of Nursing Care for Persons With Inherited Bleeding Disorders

Haemophilia, EarlyView.
ABSTRACT Introduction A nurse is one of the core members of the multidisciplinary haemophilia team. However, what people with inherited bleeding disorders (PwBD) can expect from them has not yet been formally defined. Aim This project, initiated by the EAHAD Nurses Committee, aimed to establish Principles of Nursing Care (PoNC) for PwBD to promote high‐
Nanda Uitslager, Mary Kavanagh, Maj Birkedal, Linda Myrin‐Westesson, the EAHAD Nurses Committee   +4 more
wiley   +1 more source

Outcomes of Dental Treatment Procedures in People With Haemophilia Treated Under a Comprehensive Care Model: An Analysis of Cases From a Tertiary Care Centre

Haemophilia, EarlyView.
ABSTRACT Background Haemophilia is a chronic, lifelong bleeding disorder that requires interdisciplinary care to manage and mitigate the disease burden throughout a patient's life. There is no universally accepted protocol for managing haemophilia patients during dental care.
Mathangi Kumar, Sulochana Badagabettu, Keerthilatha M. Pai, Annamma Kurien, Archana MV, Shreemathi S. Mayya, Sreejith Govindan   +6 more
wiley   +1 more source

A polymorphic Xba I site within the human von Willebrand factor (vWF) gene identified by a vWF cDNA clone [PDF]

, 1986
R. Quadt, CL Verweij, Carlie J.M. de Vries, E Briët, Hans Pannekoek   +4 more
openalex   +1 more source

Profiling of Anti‐FVIII Antibodies in Acquired Haemophilia A: ‘Insights into Domain Specificity, Isotype Variability, and Clinical Correlations’

Haemophilia, EarlyView.
ABSTRACT Introduction Acquired haemophilia A (AHA) is a rare autoimmune disorder caused by autoantibodies against coagulation factor VIII (FVIII), resulting in significant bleeding risks. Aim To characterize the anti‐FVIII antibody profile in AHA patients by assessing isotypes, subclasses, and correlations with key clinical parameters.
Ann‐Cristin Berkemeier, Isabell Matuschek, Katrin Hartlieb, Thilo Albert, Natascha Marquardt, Johannes Oldenburg, Behnaz Pezeshkpoor   +6 more
wiley   +1 more source

Venom coagglutinin: an activator of platelet aggregation dependent on von Willebrand factor.

, 1978
Marjorie S. Read, R W Shermer, K. M. Brinkhous   +2 more
openalex   +1 more source

The effect of thrombin on the complex between factor VIII and von Willebrand factor [PDF]

, 1987
R.J. Hamer, J A Koedam, Nel H. BEESER‐VISSER, Jan J. Sixma   +3 more
openalex   +1 more source