Kessler CM - Search Results

1

Efficacy and safety of a VWF/FVIII concentrate (wilate^® ) in inherited von Willebrand disease patients undergoing surgical procedures.

Srivastava A, Serban M, Werner S, Schwartz BA, Kessler CM; Wonders Study Investigators. Srivastava A, et al. Among authors: kessler cm. Haemophilia. 2017 Mar;23(2):264-272. doi: 10.1111/hae.13106. Epub 2016 Dec 27. Haemophilia. 2017. PMID: 28026130 Free article. Clinical Trial.

2

Management of von Willebrand disease: a survey on current clinical practice from the haemophilia centres of North America.

Cohen AJ, Kessler CM, Ewenstein BM; Hemophilia Research Society of North America. Cohen AJ, et al. Among authors: kessler cm. Haemophilia. 2001 May;7(3):235-41. doi: 10.1046/j.1365-2516.2001.00498.x. Haemophilia. 2001. PMID: 11380626

3

Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study.

Mannucci PM, Chediak J, Hanna W, Byrnes J, Ledford M, Ewenstein BM, Retzios AD, Kapelan BA, Schwartz RS, Kessler C; Alphanate Study Group. Mannucci PM, et al. Blood. 2002 Jan 15;99(2):450-6. doi: 10.1182/blood.v99.2.450. Blood. 2002. PMID: 11781224 Free article. Clinical Trial.

4

The safety and efficacy of B-domain deleted recombinant factor VIII concentrate in patients with severe haemophilia A.

Lusher JM, Lee CA, Kessler CM, Bedrosian CL; ReFacto Phase 3 Study Group. Lusher JM, et al. Among authors: kessler cm. Haemophilia. 2003 Jan;9(1):38-49. doi: 10.1046/j.1365-2516.2003.00708.x. Haemophilia. 2003. PMID: 12558777 Clinical Trial.

5

B-domain deleted recombinant factor VIII preparations are bioequivalent to a monoclonal antibody purified plasma-derived factor VIII concentrate: a randomized, three-way crossover study.

Kessler CM, Gill JC, White GC 2nd, Shapiro A, Arkin S, Roth DA, Meng X, Lusher JM. Kessler CM, et al. Haemophilia. 2005 Mar;11(2):84-91. doi: 10.1111/j.1365-2516.2005.01068.x. Haemophilia. 2005. PMID: 15810908 Clinical Trial.

6

Dose effect and efficacy of rFVIIa in the treatment of haemophilia patients with inhibitors: analysis from the Hemophilia and Thrombosis Research Society Registry.

Parameswaran R, Shapiro AD, Gill JC, Kessler CM; HTRS Registry Investigators. Parameswaran R, et al. Among authors: kessler cm. Haemophilia. 2005 Mar;11(2):100-6. doi: 10.1111/j.1365-2516.2005.01075.x. Haemophilia. 2005. PMID: 15810910

7

ReFacto and Advate: a single-dose, randomized, two-period crossover pharmacokinetics study in subjects with haemophilia A.

Di Paola J, Smith MP, Klamroth R, Mannucci PM, Kollmer C, Feingold J, Kessler C, Pollmann H, Morfini M, Udata C, Rothschild C, Hermans C, Janco R. Di Paola J, et al. Haemophilia. 2007 Mar;13(2):124-30. doi: 10.1111/j.1365-2516.2006.01420.x. Haemophilia. 2007. PMID: 17286764 Clinical Trial.

8

Multiple congenital coagulopathies co-expressed with Von Willebrand's disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature.

Asatiani E, Kessler CM; Directors of the Comprehensive Hemophilia Treatment Centers in Region III. Asatiani E, et al. Among authors: kessler cm. Haemophilia. 2007 Nov;13(6):685-96. doi: 10.1111/j.1365-2516.2007.01541.x. Haemophilia. 2007. PMID: 17973844 Review.

9

Diagnosis and treatment of von Willebrand disease: new perspectives and nuances.

Kessler CM. Kessler CM. Haemophilia. 2007 Dec;13 Suppl 5:3-14. doi: 10.1111/j.1365-2516.2007.01581.x. Haemophilia. 2007. PMID: 18078392 Review. No abstract available.

10

Epidemiology and general guidelines of the management of acquired haemophilia and von Willebrand syndrome.

Collins P, Budde U, Rand JH, Federici AB, Kessler CM. Collins P, et al. Among authors: kessler cm. Haemophilia. 2008 Jul;14 Suppl 3:49-55. doi: 10.1111/j.1365-2516.2008.01745.x. Haemophilia. 2008. PMID: 18510522 Review. No abstract available.

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