Carson N - Search Results

1

Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study.

Rodger MA, Walker MC, Smith GN, Wells PS, Ramsay T, Langlois NJ, Carson N, Carrier M, Rennicks White R, Shachkina S, Wen SW. Rodger MA, et al. Among authors: carson n. J Thromb Haemost. 2014 Apr;12(4):469-78. doi: 10.1111/jth.12509. J Thromb Haemost. 2014. PMID: 24447367 Free article.

2

Non-OO blood type influences the risk of recurrent venous thromboembolism. A cohort study.

Gándara E, Kovacs MJ, Kahn SR, Wells PS, Anderson DA, Chagnon I, Le Gal G, Solymoss S, Crowther M, Carrier M, Langlois N, Kovacs J, Little Ma J, Carson N, Ramsay T, Rodger MA. Gándara E, et al. Among authors: carson n. Thromb Haemost. 2013 Dec;110(6):1172-9. doi: 10.1160/TH13-06-0488. Epub 2013 Sep 26. Thromb Haemost. 2013. PMID: 24067945

3

The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism.

Wells PS, Rodger MA, Forgie MA, Langlois NJ, Armstrong L, Carson NL, Jaffey J. Wells PS, et al. Thromb Haemost. 2003 Nov;90(5):829-34. doi: 10.1160/TH03-03-0170. Thromb Haemost. 2003. PMID: 14597977

4

The factor XIII Val34Leu polymorphism: is it protective against idiopathic venous thromboembolism?

Wells PS, Anderson JL, Rodger MA, Carson N, Grimwood RL, Doucette SP. Wells PS, et al. Among authors: carson n. Blood Coagul Fibrinolysis. 2006 Oct;17(7):533-8. doi: 10.1097/01.mbc.0000245295.79891.86. Blood Coagul Fibrinolysis. 2006. PMID: 16988547

5

The risk of dialysis access thrombosis is related to the transforming growth factor-beta1 production haplotype and is modified by polymorphisms in the plasminogen activator inhibitor-type 1 gene.

Lazo-Langner A, Knoll GA, Wells PS, Carson N, Rodger MA. Lazo-Langner A, et al. Among authors: carson n. Blood. 2006 Dec 15;108(13):4052-8. doi: 10.1182/blood-2006-06-028902. Epub 2006 Aug 24. Blood. 2006. PMID: 16931622 Free article. Clinical Trial.

6

Connexin gene mutations among Ugandan patients with nonsyndromic sensorineural hearing loss.

Javidnia H, Carson N, Awubwa M, Byaruhanga R, Mack D, Vaccani JP. Javidnia H, et al. Among authors: carson n. Laryngoscope. 2014 Sep;124(9):E373-6. doi: 10.1002/lary.24697. Epub 2014 May 2. Laryngoscope. 2014. PMID: 24706568

7

Compound heterozygosity for a novel nine-nucleotide deletion and the Asn45Ser missense mutation in the glycoprotein IX gene in a patient with Bernard-Soulier syndrome.

Drouin J, Carson NL, Laneuville O. Drouin J, et al. Am J Hematol. 2005 Jan;78(1):41-8. doi: 10.1002/ajh.20236. Am J Hematol. 2005. PMID: 15609295 Free article.

8

A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center.

Gilpin CA, Carson N, Hunter AG. Gilpin CA, et al. Among authors: carson n. Clin Genet. 2000 Oct;58(4):299-308. doi: 10.1034/j.1399-0004.2000.580408.x. Clin Genet. 2000. PMID: 11076055

9

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Richer J, Daoud H, Geier P, Jarinova O, Carson N, Feberova J, Ben Fadel N, Unrau J, Bareke E, Khatchadourian K, Bulman DE, Majewski J, Boycott KM, Dyment DA. Richer J, et al. Among authors: carson n. Am J Med Genet A. 2015 Jul;167(7):1654-8. doi: 10.1002/ajmg.a.37067. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25899979

10

Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay.

Daoud H, Zhang D, McMurray F, Yu A, Luco SM, Vanstone J, Jarinova O, Carson N, Wickens J, Shishodia S, Choi H, McDonough MA, Schofield CJ, Harper ME, Dyment DA, Armour CM. Daoud H, et al. Among authors: carson n. J Med Genet. 2016 Mar;53(3):200-7. doi: 10.1136/jmedgenet-2015-103399. Epub 2015 Sep 16. J Med Genet. 2016. PMID: 26378117

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