Pediatric Clinics of North America - CIPERJ
Pediatric Clinics of North America - CIPERJ
Pediatric Clinics of North America - CIPERJ
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
VON WILLEBRAND DISEASE<br />
391<br />
[24] Fressinaud E, Veyradier A, Truchaud F, et al. Screening for von Willebrand disease with<br />
a new analyzer using high shear stress: a study <strong>of</strong> 60 cases. Blood 1998;91:1325–31.<br />
[25] Favaloro EJ. The utility <strong>of</strong> the PFA-100 in the identification <strong>of</strong> von Willebrand disease:<br />
a concise review. Semin Thromb Hemost 2006;32:537–45.<br />
[26] Howard MA, Firkin BG. Ristocetinda new tool in the investigation <strong>of</strong> platelet aggregation.<br />
Thromb Diath Haemorrh 1971;26:362–9.<br />
[27] Cooney KA, Lyons SE, Ginsburg D. Functional analysis <strong>of</strong> a type IIB von Willebrand<br />
disease missense mutation: increased binding <strong>of</strong> large von Willebrand factor multimers to<br />
platelets. Proc Natl Acad Sci U S A 1992;89:2869–72.<br />
[28] Hoyer LW, Rizza CR, Tuddenham EGD, et al. Von Willebrand factor multimer patterns in<br />
von Willebrand’s disease. Br J Haematol 1983;55:493–507.<br />
[29] Gill JC, Endres-Brooks J, Bauer PJ, et al. The effect <strong>of</strong> ABO blood group on the diagnosis <strong>of</strong><br />
von Willebrand disease. Blood 1987;69:1691–5.<br />
[30] Casonato A, Pontara E, Bertomoro A, et al. Fainting induces an acute increase in the<br />
concentration <strong>of</strong> plasma factor VIII and von Willebrand factor. Haematologica 2003;88:<br />
688–93.<br />
[31] Stakiw J, Bowman M, Hegadorn C, et al. The effect <strong>of</strong> exercise on von Willebrand factor and<br />
ADAMTS-13 in individuals with type 1 and type 2B von Willebrand disease. J Thromb<br />
Haemost 2008;6:90–6.<br />
[32] Kadir RA, Chi C. Women and von Willebrand disease: controversies in diagnosis and<br />
management. Semin Thromb Hemost 2006;32:605–15.<br />
[33] Andrew M, Vegh P, Johnston M, et al. Maturation <strong>of</strong> the hemostatic system during<br />
childhood. Blood 1992;80:1998–2005.<br />
[34] Sosothikul D, Seksarn P, Lusher JM. <strong>Pediatric</strong> reference values for molecular markers in<br />
hemostasis. J Pediatr Hematol Oncol 2007;29:19–22.<br />
[35] Sadler JE, Budde U, Eikenboom JC, et al. Update on the pathophysiology and classification<br />
<strong>of</strong> von Willebrand disease: a report <strong>of</strong> the Subcommittee on von Willebrand Factor.<br />
J Thromb Haemost 2006;4:2103–14.<br />
[36] Sadler JE. Von Willebrand disease type 1: a diagnosis in search <strong>of</strong> a disease. Blood 2003;101:<br />
2089–93.<br />
[37] James PD, Notley C, Hegadorn C, et al. The mutational spectrum <strong>of</strong> type 1 von Willebrand<br />
disease: results from a Canadian cohort study. Blood 2007;109:145–54.<br />
[38] Goodeve A, Eikenboom J, Castaman G, et al. Phenotype and genotype <strong>of</strong> a cohort <strong>of</strong><br />
families historically diagnosed with type 1 von Willebrand disease in the European study,<br />
molecular and clinical markers for the diagnosis and management <strong>of</strong> Type 1 von Willebrand<br />
disease (MCMDM-1VWD). Blood 2007;109:112–21.<br />
[39] O’Brien LA, James PD, Othman M, et al. Founder von Willebrand factor haplotype associated<br />
with type 1 von Willebrand disease. Blood 2003;102:549–57.<br />
[40] Lyons SE, Bruck ME, Bowie EJW, et al. Impaired intracellular transport produced by<br />
a subset <strong>of</strong> type IIA von Willebrand disease mutations. J Biol Chem 1992;267:4424–30.<br />
[41] Ruggeri ZM, Pareti FI, Mannucci PM, et al. Heightened interaction between platelets and<br />
factor VIII/von Willebrand factor in a new subtype <strong>of</strong> von Willebrand’s disease. N Engl J<br />
Med 1980;302:1047–51.<br />
[42] Miller JL, Castella A. Platelet-type von Willebrand’s disease: characterization <strong>of</strong> a new<br />
bleeding disorder. Blood 1982;60:790–4.<br />
[43] Brychaert MC, Pietu G, Ruan C, et al. Abnormality <strong>of</strong> glycoprotein Ib in two cases <strong>of</strong><br />
‘‘pseudo’’ von Willebrand’s disease. J Lab Clin Med 1985;106:393–400.<br />
[44] Mancuso DJ, Kroner PA, Christopherson PA, et al. Type 2M:Milwaukee-1 von Willebrand<br />
disease: an in-frame deletion in the Cys509-Cys695 loop <strong>of</strong> the von Willebrand<br />
factor A1 domain causes deficient binding <strong>of</strong> von Willebrand factor to platelets. Blood<br />
1996;88:2559–68.<br />
[45] Mazurier C. von Willebrand disease masquerading as haemophilia A. Thromb Haemost<br />
1992;67:391–6.