{"id":173,"date":"2017-04-10T22:34:55","date_gmt":"2017-04-11T03:34:55","guid":{"rendered":"http:\/\/bcmflash.aberdream.bergbuilds.domains\/blog\/?page_id=173"},"modified":"2017-04-18T06:51:56","modified_gmt":"2017-04-18T11:51:56","slug":"vwd-references","status":"publish","type":"page","link":"https:\/\/bcmflash.aberdream.bergbuilds.domains\/blog\/von-williebrand-disease\/vwd-references\/","title":{"rendered":"VWD References"},"content":{"rendered":"

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References:<\/p>\n

Berntorp, E., and T. Abshire. 2006. \u201cThe von Willebrand Disease Prophylaxis Network: Exploring a Treatment Concept.\u201d Journal of Thrombosis & Haemostasis<\/em> 4 (11): 2511\u201312. doi:10.1111\/j.1538-7836.2006.02179.x.<\/a><\/p>\n

Castaman, Giancarlo. 2013. \u201cChanges of von Willebrand Factor during Pregnancy in Women with and without von Willebrand Disease.\u201d Mediterranean Journal of Hematology and Infectious Diseases<\/em> 5 (1). doi:10.4084\/MJHID.2013.052.<\/a><\/p>\n

James, Paula D., and Anne C. Goodeve. 2011. \u201cVon Willebrand Disease.\u201d Genetics in Medicine<\/em> 13 (5): 365\u201376. doi:10.1097\/GIM.0b013e3182035931.<\/a><\/p>\n

James, P.D., and D. Lillicrap. 2013. \u201cThe Molecular Characterization of von Willebrand Disease: Good in Parts.\u201d British Journal of Haematology<\/em> 161 (2): 166\u201376. doi:10.1111\/bjh.12249.<\/a><\/p>\n

Lassila, R., and O. Lindberg. 2013. \u201cErik von Willebrand.\u201d Haemophilia<\/em> 19 (5): 643\u201347. doi:10.1111\/hae.12243.<\/a><\/p>\n

Lillicrap, D. 2009. \u201cGenotype\/Phenotype Association in von Willebrand Disease: Is the Glass Half Full or Empty?\u201d Journal of Thrombosis and Haemostasis<\/em> 7 (July): 65\u201370. doi:10.1111\/j.1538-7836.2009.03367.x.<\/a><\/p>\n

Lillicrap, David. 2013a. \u201cTranslational Medicine Advances in von Willebrand Disease.\u201d Journal of Thrombosis and Haemostasis\u202f: JTH<\/em> 11 (0 1): 75\u201383. doi:10.1111\/jth.12257.<\/a><\/p>\n

Lillicrap, David. 2013b. \u201cVon Willebrand Disease: Advances in Pathogenetic Understanding, Diagnosis, and Therapy.\u201d Blood<\/em> 122 (23): 3735\u201340. doi:10.1182\/blood-2013-06-498303.<\/a><\/p>\n

Mancuso, D. J., E. A. Tuley, L. A. Westfield, N. K. Worrall, B. B. Shelton-Inloes, J. M. Sorace, Y. G. Alevy, and J. E. Sadler. 1989. \u201cStructure of the Gene for Human von Willebrand Factor.\u201d Journal of Biological Chemistry<\/em> 264 (33): 19514\u201327.<\/a><\/p>\n

Michaux, Gr\u00e9goire, Kate B. Abbitt, Lucy M. Collinson, Sandra L. Haberichter, Keith E. Norman, and Daniel F. Cutler. 2006. \u201cThe Physiological Function of von Willebrand\u2019s Factor Depends on Its Tubular Storage in Endothelial Weibel-Palade Bodies.\u201d Developmental Cell<\/em> 10 (2): 223\u201332. doi:10.1016\/j.devcel.2005.12.012.<\/a><\/p>\n

Neff, Anne T. 2015. \u201cCurrent Controversies in the Diagnosis and Management of von Willebrand Disease.\u201d Therapeutic Advances in Hematology<\/em> 6 (4): 209\u201316. doi:10.1177\/2040620715587879.<\/a><\/p>\n

Ng, Christopher, David G. Motto, and Jorge Di Paola. 2015. \u201cDiagnostic Approach to von Willebrand Disease.\u201d Blood<\/em> 125 (13): 2029\u201337. doi:10.1182\/blood-2014-08-528398.<\/a><\/p>\n

O\u2019Brien, Lee A., Paula D. James, Maha Othman, Ergul Berber, Cherie Cameron, Colleen R. P. Notley, Carol A. Hegadorn, et al. 2003. \u201cFounder von Willebrand Factor Haplotype Associated with Type 1 von Willebrand Disease.\u201d Blood<\/em> 102 (2): 549\u201357. doi:10.1182\/blood-2002-12-3693.<\/a><\/p>\n

Owens, Colleen. 2007. \u201cErik Adolf von Willebrand: 1870-1949.\u201d Healio HemOnc Today<\/em>. July. http:\/\/www.healio.com\/hematology-oncology\/news\/print\/hemonc-today\/%7B6ab2a444-5eee-4a94-aabc-fb7621e133fd%7D\/erik-adolf-von-willebrand-1870-1949.<\/a><\/p>\n

Pruss, Cynthia M., Mia Golder, Andrea Bryant, Carol A. Hegadorn, Erin Burnett, Kimberly Laverty, Kate Sponagle, et al. 2011. \u201cPathologic Mechanisms of Type 1 VWD Mutations R1205H and Y1584C through in Vitro and in Vivo Mouse Models.\u201d Blood<\/em> 117 (16): 4358\u201366. doi:10.1182\/blood-2010-08-303727.<\/a><\/p>\n

Rydz, Natalia, Julie Grabell, David Lillicrap, and Paula D. James. 2015. \u201cChanges in von Willebrand Factor Level and von Willebrand Activity with Age in Type 1 von Willebrand Disease.\u201d Haemophilia\u202f: The Official Journal of the World Federation of Hemophilia<\/em> 21 (5): 636\u201341. doi:10.1111\/hae.12664.<\/a><\/p>\n

Sadler, J. E., U. Budde, J. C. J. Eikenboom, E. J. Favaloro, F. G. H. Hill, L. Holmberg, J. Ingerslev, et al. 2006. \u201cUpdate on the Pathophysiology and Classification of von Willebrand Disease: A Report of the Subcommittee on von Willebrand Factor.\u201d Journal of Thrombosis and Haemostasis<\/em> 4 (10): 2103\u201314. doi:10.1111\/j.1538-7836.2006.02146.x.<\/a><\/p>\n

Sadler, J. Evan. 2003. \u201cVon Willebrand Disease Type 1: A Diagnosis in Search of a Disease.\u201d Blood<\/em> 101 (6): 2089\u201393. doi:10.1182\/blood-2002-09-2892.<\/a><\/p>\n

Smeets, Michel W. J., Ruben Bierings, Henriet Meems, Frederik P. J. Mul, Dirk Geerts, Alexander P. J. Vlaar, Jan Voorberg, and Peter L. Hordijk. 2017. \u201cPlatelet-Independent Adhesion of Calcium-Loaded Erythrocytes to von Willebrand Factor.\u201d PLOS ONE<\/em> 12 (3): e0173077. doi:10.1371\/journal.pone.0173077.<\/a><\/p>\n

Starke, Richard D., Koralia E. Paschalaki, Clare E. F. Dyer, Kimberly J. Harrison-Lavoie, Jacqueline A. Cutler, Thomas A. J. McKinnon, Carolyn M. Millar, Daniel F. Cutler, Mike A. Laffan, and Anna M. Randi. 2013. \u201cCellular and Molecular Basis of von Willebrand Disease: Studies on Blood Outgrowth Endothelial Cells.\u201d Blood<\/em> 121 (14): 2773\u201384. doi:10.1182\/blood-2012-06-435727.<\/a><\/p>\n

Veyradier, Agn\u00e8s, Pierre Boisseau, Edith Fressinaud, Claudine Caron, Catherine Ternisien, Mathilde Giraud, Christophe Zawadzki, et al. 2016. \u201cA Laboratory Phenotype\/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease.\u201d Medicine<\/em> 95 (11). doi:10.1097\/MD.0000000000003038.<\/a><\/p>\n

Xie, Lijuan, Colin N. Chesterman, and Philip J. Hogg. 2001. \u201cControl of Von Willebrand Factor Multimer Size by Thrombospondin-1.\u201d The Journal of Experimental Medicine<\/em> 193 (12): 1341\u201350.<\/a><\/p>\n

Yadegari, Hamideh, Arijit Biswas, Mohammad Suhail Akhter, Julia Driesen, Vytautas Ivaskevicius, Natascha Marquardt, and Johannes Oldenburg. 2016. \u201cIntron Retention Resulting from a Silent Mutation in the VWF Gene That Structurally Influences the 5\u2032 Splice Site.\u201d Blood<\/em> 128 (17): 2144\u201352. doi:10.1182\/blood-2016-02-699686.<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

References: Berntorp, E., and T. Abshire. 2006. \u201cThe von Willebrand Disease Prophylaxis Network: Exploring a Treatment Concept.\u201d Journal of Thrombosis & Haemostasis 4 (11): 2511\u201312. doi:10.1111\/j.1538-7836.2006.02179.x. Castaman, Giancarlo. 2013. \u201cChanges of von Willebrand Factor during Pregnancy in Women with and without von Willebrand Disease.\u201d Mediterranean…<\/span><\/p>\n

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