Lusher JM - Search Results

1

Phenotypes of allo- and autoimmune antibody responses to FVIII characterized by surface plasmon resonance.

Lewis KB, Hughes RJ, Epstein MS, Josephson NC, Kempton CL, Kessler CM, Key NS, Howard TE, Kruse-Jarres R, Lusher JM, Walsh CE, Watts RG, Ettinger RA, Pratt KP; PATH (Personalized Alternative Therapies for Haemophilia) Study Investigators. Lewis KB, et al. Among authors: lusher jm. PLoS One. 2013 May 8;8(5):e61120. doi: 10.1371/journal.pone.0061120. Print 2013. PLoS One. 2013. PMID: 23667433 Free PMC article.

2

The use of purified clotting factor concentrates in hemophilia. Influence of viral safety, cost, and supply on therapy.

Pierce GF, Lusher JM, Brownstein AP, Goldsmith JC, Kessler CM. Pierce GF, et al. Among authors: lusher jm. JAMA. 1989 Jun 16;261(23):3434-8. JAMA. 1989. PMID: 2498537 Review.

3

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. Among authors: lusher jm. Haemophilia. 2005 Mar;11(2):84-91. doi: 10.1111/j.1365-2516.2005.01068.x. Haemophilia. 2005. PMID: 15810908 Clinical Trial.

4

Recent evolution of clotting factor concentrates for hemophilia A and B. Transfusion Practices Committee.

Kasper CK, Lusher JM. Kasper CK, et al. Among authors: lusher jm. Transfusion. 1993 May;33(5):422-34. doi: 10.1046/j.1537-2995.1993.33593255605.x. Transfusion. 1993. PMID: 8488548 Review. No abstract available.

5

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. Haemophilia. 2003 Jan;9(1):38-49. doi: 10.1046/j.1365-2516.2003.00708.x. Haemophilia. 2003. PMID: 12558777 Clinical Trial.

6

Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006).

Chitlur M, Warrier I, Rajpurkar M, Lusher JM. Chitlur M, et al. Among authors: lusher jm. Haemophilia. 2009 Sep;15(5):1027-31. doi: 10.1111/j.1365-2516.2009.02039.x. Epub 2009 Jun 10. Haemophilia. 2009. PMID: 19515028

7

The use of porcine factor VIII concentrate (Hyate:C) in the treatment of patients with inhibitor antibodies to factor VIII. A multicenter US experience.

Brettler DB, Forsberg AD, Levine PH, Aledort LM, Hilgartner MW, Kasper CK, Lusher JM, McMillan C, Roberts H. Brettler DB, et al. Among authors: lusher jm. Arch Intern Med. 1989 Jun;149(6):1381-5. Arch Intern Med. 1989. PMID: 2499293 Clinical Trial.

8

Human recombinant DNA-derived antihaemophilic factor (factor VIII) in the treatment of haemophilia A: conclusions of a 5-year study of home therapy. The KOGENATE Study Group.

Seremetis S, Lusher JM, Abildgaard CF, Kasper CK, Allred R, Hurst D. Seremetis S, et al. Among authors: lusher jm. Haemophilia. 1999 Jan;5(1):9-16. doi: 10.1046/j.1365-2516.1999.00191.x. Haemophilia. 1999. PMID: 10215942 Clinical Trial.

9

Thromboelastography in children with coagulation factor deficiencies.

Chitlur M, Warrier I, Rajpurkar M, Hollon W, Llanto L, Wiseman C, Lusher JM. Chitlur M, et al. Among authors: lusher jm. Br J Haematol. 2008 Jun;142(2):250-6. doi: 10.1111/j.1365-2141.2008.07063.x. Epub 2008 May 19. Br J Haematol. 2008. PMID: 18492116 Free article.

10

Decreased clearance of von Willebrand factor in a patient with type 2B von Willebrand disease following development of immune thrombocytopenia.

Wang ZJ, Onwuzurike N, Callaghan MU, Rajpurkar M, Chitlur M, Lusher JM. Wang ZJ, et al. Among authors: lusher jm. Pediatr Blood Cancer. 2008 Sep;51(3):416-8. doi: 10.1002/pbc.21593. Pediatr Blood Cancer. 2008. PMID: 18493997 Free article.

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