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[Von Willebrand disease : diagnosis and management].
Antony C, Rossaint R, Schaelte G. Antony C, et al. Internist (Berl). 2010 Sep;51(9):1118, 1120-6. doi: 10.1007/s00108-009-2491-y. Internist (Berl). 2010. PMID: 20012256 Review. German.
Inherited Von Willebrand's disease has been subdivided into 3 categories that reflect pathophysiology: partial quantitative deficiency of VWF (Type 1), qualitative deficiency (Type 2) and total deficiency (Type 3). The major clinical hallmark in Von Willebrand's disease is …
Inherited Von Willebrand's disease has been subdivided into 3 categories that reflect pathophysiology: partial quantitative deficiency of VW …
Pseudo (platelet-type) von Willebrand disease in pregnancy: a case report.
Grover N, Boama V, Chou MR. Grover N, et al. BMC Pregnancy Childbirth. 2013 Jan 17;13:16. doi: 10.1186/1471-2393-13-16. BMC Pregnancy Childbirth. 2013. PMID: 23327637 Free PMC article.
Psuedo von Willebrand disease in pregnancy can be confused with a number of other differential diagnoses, such as gestational thrombocutopenia, idiopathatic thrombocytopenia, thrombotic thrombocytopenic purpura and pre-eclampsia; all need consideration during investigations even …
Psuedo von Willebrand disease in pregnancy can be confused with a number of other differential diagnoses, such as gestational thrombocutopen …
PT-VWD posing diagnostic and therapeutic challenges - small case series.
Sánchez-Luceros A, Woods AI, Bermejo E, Shukla S, Acharya S, Lavin M, Rydz N, Othman M. Sánchez-Luceros A, et al. Platelets. 2017 Jul;28(5):484-490. doi: 10.1080/09537104.2016.1237625. Epub 2016 Nov 7. Platelets. 2017. PMID: 27819553
We describe four PT-VWD cases confirmed by genetic analysis in which either the diagnosis and/or the treatment posed challenge. We provide the details of the clinical presentation, laboratory analysis, and the treatment and the responses in each case. ...Progressive thromb …
We describe four PT-VWD cases confirmed by genetic analysis in which either the diagnosis and/or the treatment posed challenge. We provide t …
Synergistic shortening of the bleeding time by desmopressin and ethamsylate in patients with various constitutional bleeding disorders.
Kobrinsky NL, Israels ED, Bickis MG. Kobrinsky NL, et al. Am J Pediatr Hematol Oncol. 1991 Winter;13(4):437-41. doi: 10.1097/00043426-199124000-00008. Am J Pediatr Hematol Oncol. 1991. PMID: 1785670
The bleeding disorders studied included Glanzmann's thrombasthenia (one), other disorders of platelet function (four), pseudo-von Willebrand disease (one), and von Willebrand disease type I (three), type II (two), and type III (one). ...
The bleeding disorders studied included Glanzmann's thrombasthenia (one), other disorders of platelet function (four), pseudo-von …
Recombinant activated factor VII (NovoSeven) treatment of platelet-related bleeding disorders. International Registry on Recombinant Factor VIIa and Congenital Platelet Disorders Group.
Poon MC, d'Oiron R. Poon MC, et al. Blood Coagul Fibrinolysis. 2000 Apr;11 Suppl 1:S55-68. Blood Coagul Fibrinolysis. 2000. PMID: 10850567
Cases include seven patients with congenital platelet disorders [Glanzmann thrombasthenia (n = 5), Bernard-Soulier syndrome (n = 1), platelet type (pseudo-) von Willebrand disease (n = 1)] and two patients with acquired thrombocytopathy associated with …
Cases include seven patients with congenital platelet disorders [Glanzmann thrombasthenia (n = 5), Bernard-Soulier syndrome (n = 1), platele …
Pregnancy in platelet-type VWD: a case series.
O'Connor D, Lester W, Willoughby S, Wilde JT. O'Connor D, et al. Thromb Haemost. 2011 Aug;106(2):386-7. doi: 10.1160/TH11-02-0108. Epub 2011 May 26. Thromb Haemost. 2011. PMID: 21614417 No abstract available.