Friedman KD - Search Results

1

Limitations of the ristocetin cofactor assay in measurement of von Willebrand factor function.

Flood VH, Friedman KD, Gill JC, Morateck PA, Wren JS, Scott JP, Montgomery RR. Flood VH, et al. Among authors: friedman kd. J Thromb Haemost. 2009 Nov;7(11):1832-9. doi: 10.1111/j.1538-7836.2009.03594.x. Epub 2009 Aug 19. J Thromb Haemost. 2009. PMID: 19694940 Free PMC article.

2

Abnormal binding of factor VIII is linked with the substitution of glutamine for arginine 91 in von Willebrand factor in a variant form of von Willebrand disease.

Kroner PA, Friedman KD, Fahs SA, Scott JP, Montgomery RR. Kroner PA, et al. Among authors: friedman kd. J Biol Chem. 1991 Oct 15;266(29):19146-9. J Biol Chem. 1991. PMID: 1918030 Free article.

3

Enzymatic amplification of specific cDNA inserts from lambda gt11 libraries.

Friedman KD, Rosen NL, Newman PJ, Montgomery RR. Friedman KD, et al. Nucleic Acids Res. 1988 Sep 12;16(17):8718. doi: 10.1093/nar/16.17.8718. Nucleic Acids Res. 1988. PMID: 2843825 Free PMC article.

4

Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.

Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedman KD, Montgomery RR. Hessner MJ, et al. Among authors: friedman kd. Thromb Haemost. 1999 May;81(5):733-8. Thromb Haemost. 1999. PMID: 10365746

5

Contribution of the glycoprotein Ia 807TT, methylene tetrahydrofolate reductase 677TT and prothrombin 20210GA genotypes to prothrombotic risk among factor V 1691GA (Leiden) carriers.

Hessner MJ, Dinauer DM, Luhm RA, Endres JL, Montgomery RR, Friedman KD. Hessner MJ, et al. Among authors: friedman kd. Br J Haematol. 1999 Jul;106(1):237-9. doi: 10.1046/j.1365-2141.1999.01514.x. Br J Haematol. 1999. PMID: 10444193 Free article.

6

Measurement of von Willebrand factor cleaving protease (ADAMTS-13): results of an international collaborative study involving 11 methods testing the same set of coded plasmas.

Tripodi A, Chantarangkul V, Böhm M, Budde U, Dong JF, Friedman KD, Galbusera M, Girma JP, Moake J, Rick ME, Studt JD, Turecek PL, Mannucci PM. Tripodi A, et al. Among authors: friedman kd. J Thromb Haemost. 2004 Sep;2(9):1601-9. doi: 10.1111/j.1538-7836.2004.00879.x. J Thromb Haemost. 2004. PMID: 15333037 Free article.

7

Genetic mutations in von Willebrand disease identified by DHPLC and DNA sequence analysis.

Kakela JK, Friedman KD, Haberichter SL, Buchholz NP, Christopherson PA, Kroner PA, Gill JC, Montgomery RR, Bellissimo DB. Kakela JK, et al. Among authors: friedman kd. Mol Genet Metab. 2006 Mar;87(3):262-71. doi: 10.1016/j.ymgme.2005.09.016. Mol Genet Metab. 2006. PMID: 16321553

8

Type 2B von Willebrand disease associated with the release of platelet agglutinates from megakaryocytes in the bone marrow.

Slayton WB, Patel M, Sola-Visner M, Harris N, Rivers A, Montgomery RR, Friedman KD. Slayton WB, et al. Among authors: friedman kd. J Pediatr Hematol Oncol. 2008 Sep;30(9):708-11. doi: 10.1097/MPH.0b013e31817541cd. J Pediatr Hematol Oncol. 2008. PMID: 18776767 Free PMC article.

9

Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor.

Flood VH, Gill JC, Morateck PA, Christopherson PA, Friedman KD, Haberichter SL, Branchford BR, Hoffmann RG, Abshire TC, Di Paola JA, Hoots WK, Leissinger C, Lusher JM, Ragni MV, Shapiro AD, Montgomery RR. Flood VH, et al. Among authors: friedman kd. Blood. 2010 Jul 15;116(2):280-6. doi: 10.1182/blood-2009-10-249102. Epub 2010 Mar 15. Blood. 2010. PMID: 20231421 Free PMC article.

10

Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD.

Flood VH, Lederman CA, Wren JS, Christopherson PA, Friedman KD, Hoffmann RG, Montgomery RR. Flood VH, et al. Among authors: friedman kd. J Thromb Haemost. 2010 Jun;8(6):1431-3. doi: 10.1111/j.1538-7836.2010.03869.x. Epub 2010 Mar 23. J Thromb Haemost. 2010. PMID: 20345715 Free PMC article. No abstract available.

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