Results 131 to 140 of about 523,717 (316)

Feasibility of the photoacoustic detection of haemophilia-related microbleeds: a preclinical study using isolated pig limbs

open access: yesThrombosis Journal
Background Recent advancements in haemophilia treatment have dramatically reduced the frequency of symptomatic bleeding. However, minor, asymptomatic bleeding may contribute to the progression of joint damage and decrease quality of life. Detecting small
Asuka Sakata   +10 more
doaj   +1 more source

Comparative frequency of Coagulation Factor II and Coagulation Factor V Alleles among new-born and senior citizens [PDF]

open access: yes, 2005
Resistance to activated protein C is one of the most common inherited disorders associated with hereditary thrombophilia. A missense mutation in the gene coding for coagulation factor V (CF V Leiden) and which renders this procoagulant factor resistant ...
Bezzina Wettinger, Stephanie   +4 more
core  

Optimization of plasma-based BioID identifies plasminogen as a ligand of ADAMTS13

open access: yesScientific Reports
ADAMTS13, a disintegrin and metalloprotease with a thrombospondin type 1 motif, member 13, regulates the length of Von Willebrand factor (VWF) multimers and their platelet-binding activity. ADAMTS13 is constitutively secreted as an active protease and is
Hasam Madarati   +10 more
doaj   +1 more source

Tobacco and Thrombosis [PDF]

open access: yesAmerican Journal of Public Health and the Nations Health, 1966
E A, Murphy, J F, Mustard
openaire   +2 more sources

Factor XIII Val34Leu is a genetic factor involved in the etiology of venous thrombosis

open access: yes, 1999
A mutation in the factor XIII gene (FXIII Val34Leu) gene was recently reported to confer protection against myocardial infarction, but its relationship with venous thrombosis is unknown.
Maffei, F. H.   +12 more
core  

Management of Iron Overload in Infants and Toddlers With Diamond–Blackfan Anemia Syndrome: A French–Italian Study

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Diamond–Blackfan Anemia Syndrome (DBAS) is a rare congenital anemia often requiring chronic red blood cell transfusions from infancy. Without appropriate chelation, iron overload develops early and may be severe; however, no data are available on chelation in patients under 3 years of age.
Francesca Torchio   +19 more
wiley   +1 more source

Selected and Gene Polymorphisms in Patients with Migraine and Sticky Platelet Syndrome

open access: yesClinical and Applied Thrombosis/Hemostasis
One of the most common clinical manifestations of inherited platelet hyperaggregability also known as sticky platelet syndrome (SPS) is migraine.
Tomas Simurda MD, PhD   +9 more
doaj   +1 more source

The Role of the Gut Microbiota in Allogeneic Hematopoietic Cell Transplantation

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Allogeneic hematopoietic cell transplantation (allo‐HCT) is an effective treatment for patients with high‐risk hematologic malignancies. Over the last decade, gut microbiota composition during allo‐HCT has been associated with patients' outcomes.
Wenjing Hao   +4 more
wiley   +1 more source

High incidence of thrombophilia detected in Chinese patients with venous thrombosis [PDF]

open access: yes, 1994
Venous thromboembolism is rare in Chinese. To determine the incidence and disease profile of thrombophilia in Chinese patients with thrombosis, 52 unselected Chinese patients with documented venous thrombosis were studied for the presence of ...
Liu, HW   +6 more
core  

Factor XIII Val34Leu is a genetic factor involved in the aetiology of venous thrombosis

open access: yes, 1999
A mutation in the factor XIII gene (FXIII Val34Leu) gene was recently reported to confer protection against myocardial infarction, but its relationship with venous thrombosis is unknown.
Franco, R. F.   +8 more
core  

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