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Treatment of periodontal disease results in improvements in endothelial dysfunction and reduction of the carotid intima-media thickness.
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- FASEB Journal, 2009, v. 23, n. 4, p. 1196, doi. 10.1096/fj.08-119578
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- Article
Platelet von willebrand factor abnormalities in myeloproliferative syndromes.
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- American Journal of Hematology, 1995, v. 49, n. 4, p. 289, doi. 10.1002/ajh.2830490406
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- Article
Characterization of two cases of acquired transitory von willebrand syndrome with ciprofloxacin: Evidence for heightened proteolysis of von willebrand factor.
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- American Journal of Hematology, 1995, v. 49, n. 1, p. 83, doi. 10.1002/ajh.2830490114
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- Article
Multimeric pattern of plasma and platelet von willebrand factor is normal in uremic patients.
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- American Journal of Hematology, 1993, v. 44, n. 4, p. 266, doi. 10.1002/ajh.2830440409
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- Article
Desmopressin-induced thrombocytopenia in type i platelet discordant von willebrand disease.
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- American Journal of Hematology, 1993, v. 43, n. 1, p. 5, doi. 10.1002/ajh.2830430103
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- Article
Type II H von willebrand disease: New structural abnormality of plasma and platelet von willebrand factor in a patient with prolonged bleeding time and borderline levels of ristocetin cofactor activity.
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- American Journal of Hematology, 1989, v. 32, n. 4, p. 287, doi. 10.1002/ajh.2830320409
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- Article
Subcutaneous desmopressin (DDAVP) shortens the bleeding time in uremia.
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- American Journal of Hematology, 1989, v. 31, n. 1, p. 32, doi. 10.1002/ajh.2830310106
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- Article
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutation.
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- British Journal of Haematology, 2000, v. 108, n. 1, p. 188, doi. 10.1046/j.1365-2141.2000.01807.x
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- Article
Proteolysis of von Willebrand factor is decreased in acute promyelocytic leukaemia by treatment with all-trans-retinoic acid.
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- British Journal of Haematology, 1996, v. 92, n. 3, p. 733, doi. 10.1046/j.1365-2141.1996.401939.x
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- Article
Factor VIII: C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand disease.
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- British Journal of Haematology, 1995, v. 89, n. 1, p. 147, doi. 10.1111/j.1365-2141.1995.tb08921.x
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- Article