DiMichele D - Search Results

1

Factor V Leiden, activated protein C resistance, and retinal vein occlusion.

Ciardella AP, Yannuzzi LA, Freund KB, DiMichele D, Nejat M, De Rosa JT, Daly JR, Sisco L. Ciardella AP, et al. Among authors: dimichele d. Retina. 1998;18(4):308-15. doi: 10.1097/00006982-199807000-00003. Retina. 1998. PMID: 9730172

2

Mutation in the factor VII hepatocyte nuclear factor 4α-binding site contributes to factor VII deficiency.

Zheng XW, Kudaravalli R, Russell TT, DiMichele DM, Gibb C, Russell JE, Margaritis P, Pollak ES. Zheng XW, et al. Blood Coagul Fibrinolysis. 2011 Oct;22(7):624-7. doi: 10.1097/MBC.0b013e3283497699. Blood Coagul Fibrinolysis. 2011. PMID: 21760481

3

High frequency of premature termination mutations in the factor V gene: three factor V deficiency case reports and a mutation review.

Schrijver I, Hong DW, Mandle L, Jones CD, DiMichele D, Monahan PE, Zehnder JL. Schrijver I, et al. Among authors: dimichele d. Thromb Haemost. 2005 Mar;93(3):610-1. Thromb Haemost. 2005. PMID: 15735818 No abstract available.

4

Severe and moderate haemophilia A and B in US females.

Di Michele DM, Gibb C, Lefkowitz JM, Ni Q, Gerber LM, Ganguly A. Di Michele DM, et al. Haemophilia. 2014 Mar;20(2):e136-43. doi: 10.1111/hae.12364. Haemophilia. 2014. PMID: 24533955

5

Management of pregnancy in a patient with severe haemophilia A.

Dhar P, Abramovitz S, DiMichele D, Gibb CB, Gadalla F. Dhar P, et al. Among authors: dimichele d. Br J Anaesth. 2003 Sep;91(3):432-5. doi: 10.1093/bja/aeg177. Br J Anaesth. 2003. PMID: 12925488 Free article.

6

Use of global assays to understand clinical phenotype in congenital factor VII deficiency.

Greene LA, Goldenberg NA, Simpson ML, Villalobos-Menuey E, Bombardier C, Acharya SS, Santiago-Borrero PJ, Cambara A, DiMichele DM. Greene LA, et al. Among authors: dimichele dm. Haemophilia. 2013 Sep;19(5):765-72. doi: 10.1111/hae.12160. Epub 2013 May 20. Haemophilia. 2013. PMID: 23682803

7

Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program.

Christopherson PA, Haberichter SL, Flood VH, Perry CL, Sadler BE, Bellissimo DB, Di Paola J, Montgomery RR; Zimmerman Program Investigators. Christopherson PA, et al. J Thromb Haemost. 2022 Jul;20(7):1576-1588. doi: 10.1111/jth.15713. Epub 2022 Apr 6. J Thromb Haemost. 2022. PMID: 35343054 Free article.

8

Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias.

Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group. Acharya SS, et al. Among authors: dimichele dm. J Thromb Haemost. 2004 Feb;2(2):248-56. doi: 10.1111/j.1538-7836.2003.t01-1-00553.x. J Thromb Haemost. 2004. PMID: 14995986 Free article.

9

Prevalence of clinical hip abnormalities in haemophilia A and B: an analysis of the UDC database.

Kelly D, C Zhang Q, M Soucie J, Manco-Johnson M, Dimichele D; Joint Outcome Subcommittee of the Coordinating Committee for the Universal Data Collection Database and the Hemophilia Treatment Center Network Investigators. Kelly D, et al. Among authors: dimichele d. Haemophilia. 2013 May;19(3):426-31. doi: 10.1111/hae.12073. Epub 2012 Dec 17. Haemophilia. 2013. PMID: 23252621 Free PMC article.

10

Inhibitors in haemophilia: a primer.

DiMichele DM. DiMichele DM. Haemophilia. 2000 Jul;6 Suppl 1:38-40. doi: 10.1046/j.1365-2516.2000.00045.x. Haemophilia. 2000. PMID: 10982266 Review. No abstract available.

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