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Results: 1 to 20 of 35

1.

Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid.

Orrú CD, Groveman BR, Hughson AG, Zanusso G, Coulthart MB, Caughey B.

MBio. 2015 Jan 20;6(1). pii: e02451-14. doi: 10.1128/mBio.02451-14.

2.

Evidence for synergistic effects of PRNP and ATP7B mutations in severe neuropsychiatric deterioration.

Forbes N, Goodwin S, Woodward K, Morgan DG, Brady L, Coulthart MB, Tarnopolsky MA.

BMC Med Genet. 2014 Feb 20;15:22. doi: 10.1186/1471-2350-15-22.

3.

Interpretation of cerebrospinal fluid protein tests in the diagnosis of sporadic Creutzfeldt-Jakob disease: an evidence-based approach.

Coulthart MB, Jansen GH, Cashman NR.

CMAJ. 2014 Jun 10;186(9):E333-9. doi: 10.1503/cmaj.130720. Epub 2014 Jan 20. Review. No abstract available.

PMID:
24446456
4.

The prion protein modulates A-type K+ currents mediated by Kv4.2 complexes through dipeptidyl aminopeptidase-like protein 6.

Mercer RC, Ma L, Watts JC, Strome R, Wohlgemuth S, Yang J, Cashman NR, Coulthart MB, Schmitt-Ulms G, Jhamandas JH, Westaway D.

J Biol Chem. 2013 Dec 27;288(52):37241-55. doi: 10.1074/jbc.M113.488650. Epub 2013 Nov 13.

5.

Insights into origins of Human T-cell Lymphotropic Virus Type 1 based on new strains from aboriginal people of Canada.

Andonov A, Coulthart MB, Pérez-Losada M, Crandall KA, Posada D, Padmore R, Giulivi A, Oger JJ, Peters AA, Dekaban GA.

Infect Genet Evol. 2012 Dec;12(8):1822-30. doi: 10.1016/j.meegid.2012.07.015. Epub 2012 Aug 13.

PMID:
22921499
6.

Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study.

Coulthart MB, Jansen GH, Olsen E, Godal DL, Connolly T, Choi BC, Wang Z, Cashman NR.

BMC Neurol. 2011 Oct 27;11:133. doi: 10.1186/1471-2377-11-133.

7.

Gerstmann-Straussler-Scheinker disease due to a novel prion protein gene mutation.

Hinnell C, Coulthart MB, Jansen GH, Cashman NR, Lauzon J, Clark A, Costello F, White C, Midha R, Wiebe S, Furtado S.

Neurology. 2011 Feb 1;76(5):485-7. doi: 10.1212/WNL.0b013e31820a0ab2. No abstract available.

PMID:
21282596
8.

Molecular, biochemical and genetic characteristics of BSE in Canada.

Dudas S, Yang J, Graham C, Czub M, McAllister TA, Coulthart MB, Czub S.

PLoS One. 2010 May 14;5(5):e10638. doi: 10.1371/journal.pone.0010638.

9.

MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.

Meissner B, Kallenberg K, Sanchez-Juan P, Collie D, Summers DM, Almonti S, Collins SJ, Smith P, Cras P, Jansen GH, Brandel JP, Coulthart MB, Roberts H, Van Everbroeck B, Galanaud D, Mellina V, Will RG, Zerr I.

Neurology. 2009 Jun 9;72(23):1994-2001. doi: 10.1212/WNL.0b013e3181a96e5d.

PMID:
19506221
10.

Species barriers for chronic wasting disease by in vitro conversion of prion protein.

Li L, Coulthart MB, Balachandran A, Chakrabartty A, Cashman NR.

Biochem Biophys Res Commun. 2007 Dec 28;364(4):796-800. Epub 2007 Oct 25.

PMID:
17964288
11.

Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002.

de Pedro-Cuesta J, Glatzel M, Almazán J, Stoeck K, Mellina V, Puopolo M, Pocchiari M, Zerr I, Kretszchmar HA, Brandel JP, Delasnerie-Lauprêtre N, Alpérovitch A, Van Duijn C, Sanchez-Juan P, Collins S, Lewis V, Jansen GH, Coulthart MB, Gelpi E, Budka H, Mitrova E.

BMC Public Health. 2006 Nov 10;6:278.

12.

A case of familial Creutzfeldt-Jakob disease presenting with dry cough.

Larue S, Verreault S, Gould P, Coulthart MB, Bergeron C, Dupré N.

Can J Neurol Sci. 2006 May;33(2):243-5.

PMID:
16736740
13.

On the phylogenetic placement of human T cell leukemia virus type 1 sequences associated with an Andean mummy.

Coulthart MB, Posada D, Crandall KA, Dekaban GA.

Infect Genet Evol. 2006 Mar;6(2):91-6. Epub 2005 Mar 23.

14.

Cellular prion protein is released on exosomes from activated platelets.

Robertson C, Booth SA, Beniac DR, Coulthart MB, Booth TF, McNicol A.

Blood. 2006 May 15;107(10):3907-11. Epub 2006 Jan 24.

15.

BARBs and the genetics of BSE.

Coulthart MB.

Vet Rec. 2004 Jan 10;154(2):61-2. No abstract available.

PMID:
14758837
16.

Prion protein gene sequence of Canada's first non-imported case of bovine spongiform encephalopathy (BSE).

Coulthart MB, Mogk R, Rancourt JM, Godal DL, Czub S.

Genome. 2003 Dec;46(6):1005-9. Erratum in: Genome. 2004 Feb;47(1):229.

PMID:
14663519
17.
18.

First case of variant Creutzfeldt-Jakob disease in Canada.

Jansen GH, Voll CL, Robinson CA, Gervais R, Sutcliffe T, Bergeron C, Coulthart MB, Giulivi A.

Can Commun Dis Rep. 2003 Jul 1;29(13):117-20. English, French. No abstract available. Erratum in: Can Commun Dis Rep. 2003 Aug 1;29(15):136.

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