Sadler JE - Search Results

1

Biochemistry and genetics of von Willebrand factor.

Sadler JE. Sadler JE. Annu Rev Biochem. 1998;67:395-424. doi: 10.1146/annurev.biochem.67.1.395. Annu Rev Biochem. 1998. PMID: 9759493 Review.

2

von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA).

Nichols WL, Hultin MB, James AH, Manco-Johnson MJ, Montgomery RR, Ortel TL, Rick ME, Sadler JE, Weinstein M, Yawn BP. Nichols WL, et al. Among authors: sadler je. Haemophilia. 2008 Mar;14(2):171-232. doi: 10.1111/j.1365-2516.2007.01643.x. Haemophilia. 2008. PMID: 18315614

3

Report on the workshop: Von Willebrand factor and Thrombotic Thrombocytopenic Purpura.

Moake JL, Sadler JE, Mannucci P, Ganguly P. Moake JL, et al. Among authors: sadler je. Am J Hematol. 2001 Oct;68(2):122-6. doi: 10.1002/ajh.1163. Am J Hematol. 2001. PMID: 11559952 No abstract available.

4

Slippery criteria for von Willebrand disease type 1.

Sadler JE. Sadler JE. J Thromb Haemost. 2004 Oct;2(10):1720-3. doi: 10.1111/j.1538-7836.2004.00933.x. J Thromb Haemost. 2004. PMID: 15456481 No abstract available.

5

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.

Sadler JE, Budde U, Eikenboom JC, Favaloro EJ, Hill FG, Holmberg L, Ingerslev J, Lee CA, Lillicrap D, Mannucci PM, Mazurier C, Meyer D, Nichols WL, Nishino M, Peake IR, Rodeghiero F, Schneppenheim R, Ruggeri ZM, Srivastava A, Montgomery RR, Federici AB; Working Party on von Willebrand Disease Classification. Sadler JE, et al. J Thromb Haemost. 2006 Oct;4(10):2103-14. doi: 10.1111/j.1538-7836.2006.02146.x. Epub 2006 Aug 2. J Thromb Haemost. 2006. PMID: 16889557 Review.

6

von Willebrand disease: a database of point mutations, insertions, and deletions. For the Consortium on von Willebrand Factor Mutations and Polymorphisms, and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Ginsburg D, Sadler JE. Ginsburg D, et al. Among authors: sadler je. Thromb Haemost. 1993 Feb 1;69(2):177-84. Thromb Haemost. 1993. PMID: 8456431 Review.

7

New variant of von Willebrand disease type II with markedly increased levels of von Willebrand factor antigen and dominant mode of inheritance: von Willebrand disease type IIC Miami.

Ledford MR, Rabinowitz I, Sadler JE, Kent JW, Civantos F. Ledford MR, et al. Among authors: sadler je. Blood. 1993 Jul 1;82(1):169-75. Blood. 1993. PMID: 8324222

8

Effect of type IIB von Willebrand disease mutation Arg(545)Cys on platelet glycoprotein Ib binding--studies with recombinant von Willebrand factor.

Inbal A, Kornbrot N, Harrison P, Randi AM, Sadler JE. Inbal A, et al. Among authors: sadler je. Thromb Haemost. 1993 Dec 20;70(6):1058-62. Thromb Haemost. 1993. PMID: 8165601

9

A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Sadler JE. Sadler JE. Thromb Haemost. 1994 Apr;71(4):520-5. Thromb Haemost. 1994. PMID: 8052974

10

Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene.

Peake IR, Bowen D, Bignell P, Liddell MB, Sadler JE, Standen G, Bloom AL. Peake IR, et al. Among authors: sadler je. Blood. 1990 Aug 1;76(3):555-61. Blood. 1990. PMID: 2378985

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