Search Results - Mathieu, Jean

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  1. 1
    Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy

    Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy by Breton, Robert, Mathieu, Jean

    Published 2009
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  2. 2
    PROTEIN-C IS THE MOST POTENT HEMATOLOGIC BIOMARKER OF OUR NOVEL HEMOSTATIC SCORE CREATED TO IDENTIFY HIGH-RISK PATIENTS WITH SEPSIS-ASSOCIATED COAGULOPATHY

    PROTEIN-C IS THE MOST POTENT HEMATOLOGIC BIOMARKER OF OUR NOVEL HEMOSTATIC SCORE CREATED TO IDENTIFY HIGH-RISK PATIENTS WITH SEPSIS-ASSOCIATED COAGULOPATHY by Mathieu, Jean-Francois, Boucher, Sylvie

    Published 2020
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  3. 3
    Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1)

    Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1) by Jean, Stéphane, Richer, Louis, Laberge, Luc, Mathieu, Jean

    Published 2014
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  4. 4
    From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay

    From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay by Gagnon, Cynthia, Brais, Bernard, Lessard, Isabelle, Lavoie, Caroline, Côté, Isabelle, Mathieu, Jean

    Published 2018
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  5. 5
    Development and validation of a disease severity index for ataxia of Charlevoix-Saguenay

    Development and validation of a disease severity index for ataxia of Charlevoix-Saguenay by Gagnon, Cynthia, Brais, Bernard, Lessard, Isabelle, Lavoie, Caroline, Côté, Isabelle, Mathieu, Jean

    Published 2019
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  6. 6
    Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes

    Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes by Overend, Gayle, Légaré, Cécilia, Mathieu, Jean, Bouchard, Luigi, Gagnon, Cynthia, Monckton, Darren G

    Published 2019
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  7. 7
    An exploratory natural history of ataxia of Charlevoix-Saguenay: A 2-year follow-up

    An exploratory natural history of ataxia of Charlevoix-Saguenay: A 2-year follow-up by Gagnon, Cynthia, Lessard, Isabelle, Lavoie, Caroline, Côté, Isabelle, St-Gelais, Raphaël, Mathieu, Jean, Brais, Bernard

    Published 2018
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  8. 8
    DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1

    DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1 by Légaré, Cécilia, Overend, Gayle, Guay, Simon-Pierre, Monckton, Darren G., Mathieu, Jean, Gagnon, Cynthia, Bouchard, Luigi

    Published 2019
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  9. 9
    Functional mobility in walking adult population with ataxia of Charlevoix-Saguenay

    Functional mobility in walking adult population with ataxia of Charlevoix-Saguenay by Lessard, Isabelle, St-Gelais, Raphaël, Hébert, Luc J., Côté, Isabelle, Mathieu, Jean, Brais, Bernard, Gagnon, Cynthia

    Published 2021
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  10. 10
    MRI-based Medical Nanorobotic Platform for the Control of Magnetic Nanoparticles and Flagellated Bacteria for Target Interventions in Human Capillaries

    MRI-based Medical Nanorobotic Platform for the Control of Magnetic Nanoparticles and Flagellated Bacteria for Target Interventions in Human Capillaries by Martel, Sylvain, Felfoul, Ouajdi, Mathieu, Jean-Baptiste, Chanu, Arnaud, Tamaz, Samer, Mohammadi, Mahmood, Mankiewicz, Martin, Tabatabaei, Nasr

    Published 2009
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  11. 11
    Towards an integrative approach to the management of myotonic dystrophy type 1

    Towards an integrative approach to the management of myotonic dystrophy type 1 by Gagnon, Cynthia, Noreau, Luc, Moxley, Richard T, Laberge, Luc, Jean, Stéphane, Richer, Louis, Perron, Michel, Veillette, Suzanne, Mathieu, Jean

    Published 2007
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  12. 12
    Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1

    Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1 by Roussel, Marie-Pier, Morin, Marika, Girardin, Mélina, Fortin, Anne-Marie, Leone, Mario, Mathieu, Jean, Gagnon, Cynthia, Duchesne, Elise

    Published 2019
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  13. 13
    High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses

    High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses by Jilani, Abdulhakim, Matviychuk, Diana, Blaser, Susan, Dyack, Sarah, Mathieu, Jean, Prasad, Asuri N., Prasad, Chitra, Kyriakopoulou, Lianna, Mercimek‐Andrews, Saadet

    Published 2019
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  14. 14
    The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

    The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care by De Antonio, Marie, Dogan, Céline, Daidj, Ferroudja, Eymard, Bruno, Puymirat, Jack, Mathieu, Jean, Gagnon, Cynthia, Katsahian, Sandrine, Hamroun, Dalil, Bassez, Guillaume

    Published 2019
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  15. 15
    Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability

    Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability by Bchetnia, Mbarka, Bouchard, Luigi, Mathieu, Jean, Campeau, Philippe M, Morin, Charles, Brisson, Diane, Laberge, Anne-Marie, Vézina, Hélène, Gaudet, Daniel, Laprise, Catherine

    Published 2021
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  16. 16
    Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation

    Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation by Tétreault, Martine, Gonzalez, Michael, Dicaire, Marie-Josée, Allard, Pierre, Gehring, Kalle, Leblanc, Diane, Leclerc, Nadine, Schondorf, Ronald, Mathieu, Jean, Zuchner, Stephan, Brais, Bernard

    Published 2015
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  17. 17
    SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases

    SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases by Choquet, Karine, Tétreault, Martine, Yang, Sharon, La Piana, Roberta, Dicaire, Marie- Josée, Vanstone, Megan R, Mathieu, Jean, Bouchard, Jean-Pierre, Rioux, Marie-France, Rouleau, Guy A, Boycott, Kym M, Majewski, Jacek, Brais, Bernard

    Published 2016
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  18. 18
    Peripheral Nerve Stimulation Characteristics of an Asymmetric Head-Only Gradient Coil Compatible with a High-Channel-Count Receiver Array

    Peripheral Nerve Stimulation Characteristics of an Asymmetric Head-Only Gradient Coil Compatible with a High-Channel-Count Receiver Array by Lee, Seung-Kyun, Mathieu, Jean-Baptiste, Graziani, Dominic, Piel, Joseph, Budesheim, Eric, Fiveland, Eric, Hardy, Christopher J., Tan, Ek Tsoon, Amm, Bruce, Foo, Thomas K.-F, Bernstein, Matt A., Huston, John, Shu, Yunhong, Schenck, John F.

    Published 2015
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  19. 19
    Prevalence and determinants of hypertension and associated cardiovascular risk factors: data from a population-based, cross-sectional survey in Saint Louis, Senegal

    Prevalence and determinants of hypertension and associated cardiovascular risk factors: data from a population-based, cross-sectional survey in Saint Louis, Senegal by Pessinaba, Soulemane, Mbaye, Alassane, Yabeta, Grâce-À-Dieu, Ndao, Cheikh Tidiane, Harouna, Habibou, Diagne, Dior, Diack, Bouna, Kane, Moussa, Kane, Abdoul, Kane, Adama, Ndiaye, Mouhamadou Bamba, Bodian, Malick, Diao, Maboury, Mbaye, Maïmouna Ndour, Niang, Khadim, Sy Mathieu, Jean-Baptiste

    Published 2013
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  20. 20
    Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians

    Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians by Pellerin, David, Aykanat, Asli, Ellezam, Benjamin, Troiano, Emily C., Karamchandani, Jason, Dicaire, Marie-Josée, Petitclerc, Marc, Robertson, Rebecca, Allard-Chamard, Xavier, Brunet, Denis, Konersman, Chamindra G., Mathieu, Jean, Chardon, Jodi Warman, Gupta, Vandana A., Beggs, Alan H., Brais, Bernard, Chrestian, Nicolas

    Published 2020
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