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Therefore, electron deficiency factor combined with steric hindrance factor inhibits the cross-linking of these PFCP polymers via free radical mechanism.
Infants with severe factor VII deficiency (factor VII 0%) invariably develop fatal intracranial hemorrhage within hours or days of birth.
A large number of outstanding researchers have identified multiple factors that genetically contribute to hypercoagulability and osteonecrosis, including protein C and protein S deficiency, factor V Leiden, prothrombin G20210A mutation, and higher lipoprotein levels [ 8– 10].
Repeat doses may be guided by ROTEM or laboratory assessment of fibrinogen levels Control of bleeding associated with fibrinogen deficiency Factor XIII deficiency Second-line therapy for vWD and haemophilia A (Factor VIII deficiency).
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Examine sleep deficiency, factors, and associations with cardiometabolic diseases in United States Native Hawaiian/Pacific Islanders (NHPI), Blacks, and Whites.
Participants had no history of diabetes mellitus, kidney diseases, thyroid diseases, alcoholism, liver disease, lung disease, or vitamin B12 deficiency, factors which could also lead to cognitive impairment.
With the study goal to identify characteristics associated with vitamin D deficiency, factors were entered into a logistic regression model.
Live donor candidates were excluded from donation if they presented any abnormalities in the hemostatic study, due to genetic mutations, anticoagulant protein deficiencies, factor VIII deficiency or high levels of anticardiolipin antibodies [ 13].
Congenital deficiency of factor V (labile factor, proaccelerin) is a rare hereditary coagulation disorder with an incidence of 1 1000,000 and is inherited as an autosomal recessive trait [ 1].
The next most common form of hemophilia, hemophilia B, is due to deficiency of factor IX (plasma thromboplastin component, or PTC).
Von Willebrand disease, inherited blood disorder characterized by a prolonged bleeding time and a deficiency of factor VIII, an important blood-clotting agent.
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