Kessler C - Search Results

1

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. Among authors: kessler c. Blood. 2002 Jan 15;99(2):450-6. doi: 10.1182/blood.v99.2.450. Blood. 2002. PMID: 11781224 Free article. Clinical Trial.

2

A prospective study of treatment of acquired (autoimmune) factor VIII inhibitors with high-dose intravenous gammaglobulin.

Schwartz RS, Gabriel DA, Aledort LM, Green D, Kessler CM. Schwartz RS, et al. Among authors: kessler cm. Blood. 1995 Jul 15;86(2):797-804. Blood. 1995. PMID: 7606010 Free article.

3

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

4

Human recombinant factor IX: safety and efficacy studies in hemophilia B patients previously treated with plasma-derived factor IX concentrates.

Roth DA, Kessler CM, Pasi KJ, Rup B, Courter SG, Tubridy KL; Recombinant Factor IX Study Group. Roth DA, et al. Among authors: kessler cm. Blood. 2001 Dec 15;98(13):3600-6. doi: 10.1182/blood.v98.13.3600. Blood. 2001. PMID: 11739163 Free article. Clinical Trial.

5

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.

6

Bleeding symptoms and laboratory correlation in patients with severe von Willebrand disease.

Metjian AD, Wang C, Sood SL, Cuker A, Peterson SM, Soucie JM, Konkle BA; HTCN Study Investigators. Metjian AD, et al. Haemophilia. 2009 Jul;15(4):918-25. doi: 10.1111/j.1365-2516.2009.02025.x. Epub 2009 Apr 7. Haemophilia. 2009. PMID: 19473418

7

von Willebrand disease in the 21st century: current approaches and new challenges.

Mannucci PM, Federici AB, James AH, Kessler CM. Mannucci PM, et al. Among authors: kessler cm. Haemophilia. 2009 Sep;15(5):1154-8. doi: 10.1111/j.1365-2516.2008.01932.x. Epub 2009 Jul 14. Haemophilia. 2009. PMID: 19624761 No abstract available.

8

Emerging clinical concerns in the ageing haemophilia patient.

Konkle BA, Kessler C, Aledort L, Andersen J, Fogarty P, Kouides P, Quon D, Ragni M, Zakarija A, Ewenstein B. Konkle BA, et al. Among authors: kessler c. Haemophilia. 2009 Nov;15(6):1197-209. doi: 10.1111/j.1365-2516.2009.02066.x. Epub 2009 Jul 21. Haemophilia. 2009. PMID: 19686466 Review.

9

von Willebrand factor: what is its role in the immune response in haemophilia?

Kaveri S, Mannucci PM, Kurth MH, Ewing N, Kessler CM, Nugent DJ, Gomperts ED. Kaveri S, et al. Among authors: kessler cm. Haemophilia. 2011 Jan;17(1):e235-8. doi: 10.1111/j.1365-2516.2010.02277.x. Haemophilia. 2011. PMID: 20546026 No abstract available.

10

Summary report of the First International Conference on inhibitors in haemophilia A.

Lacroix-Desmazes S, Scott DW, Goudemand J, Van Den Berg M, Makris M, Van Velzen AS, Santagostino E, Lillicrap D, Rosendaal FR, Hilger A, Sauna ZE, Oldenburg J, Mantovani L, Mancuso ME, Kessler C, Hay CRM, Knoebl P, Di Minno G, Hoots K, Bok A, Brooker M, Buoso E, Mannucci PM, Peyvandi F. Lacroix-Desmazes S, et al. Among authors: kessler c. Blood Transfus. 2017 Oct;15(6):568-576. doi: 10.2450/2016.0252-16. Epub 2016 Nov 25. Blood Transfus. 2017. PMID: 27893354 Free PMC article. No abstract available.

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