Search Results - Gilfix, Brian

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  1. 1
    Vitamin B(12) and homocysteine

    Vitamin B(12) and homocysteine by Gilfix, Brian M.

    Published 2005
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  2. 2
    Troponin assays for coronary syndrome diagnosis

    Troponin assays for coronary syndrome diagnosis by Gilfix, Brian M.

    Published 2002
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  3. 3
    The Use of Genetic Testing Panels for Dyslipidemia: A Quality Improvement Project at the McGill University Health Centre

    The Use of Genetic Testing Panels for Dyslipidemia: A Quality Improvement Project at the McGill University Health Centre by Pasqua, Melissa-Rosina, Pare, Aurelie, Blank, David, Gilfix, Brian

    Published 2021
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  4. 4
    Comment on Complications Following Antidotal Use of Intravenous Lipid Emulsion Therapy (Levine et al., J Med Toxicol 2013)

    Comment on Complications Following Antidotal Use of Intravenous Lipid Emulsion Therapy (Levine et al., J Med Toxicol 2013) by Grunbaum, Ami M., Gosselin, Sophie, Gilfix, Brian M., Blank, David W.

    Published 2014
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  5. 5
    Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis

    Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis by Awan, Zuhier, Aljenedil, Sumayah, Rosenblatt, David S, Cusson, Jean, Gilfix, Brian M, Genest, Jacques

    Published 2014
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  6. 6
    The role of cardiac troponin t and other new biochemical markers in evaluation and risk stratification of patients with acute chest pain syndromes

    The role of cardiac troponin t and other new biochemical markers in evaluation and risk stratification of patients with acute chest pain syndromes by Solymoss, B. Charles, Bourassa, Martial G., Wesolowska, Ewa, Dryda, Ihor, Th$Earoux, Pierre, Mondor, Louise, Perrault, Danielle, Gilfix, Brian Mark

    Published 2009
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  7. 7
    Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23A

    Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23A by Gupta, Swati, Fahiminiya, Somayyeh, Wang, Tracy, Dempsey Nunez, Laura, Rosenblatt, David S., Gibson, William T., Gilfix, Brian, Bergeron, John J. M., Jerome-Majewska, Loydie A.

    Published 2016
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  8. 8
    The novel aminoglycoside, ELX-02, permits CTNS(W138X) translational read-through and restores lysosomal cystine efflux in cystinosis

    The novel aminoglycoside, ELX-02, permits CTNS(W138X) translational read-through and restores lysosomal cystine efflux in cystinosis by Brasell, Emma J., Chu, Lee Lee, Akpa, Murielle M., Eshkar-Oren, Idit, Alroy, Iris, Corsini, Rachel, Gilfix, Brian M., Yamanaka, Yojiro, Huertas, Pedro, Goodyer, Paul

    Published 2019
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