نتائج البحث - Mathieu, Jean
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From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay حسب Gagnon, Cynthia, Brais, Bernard, Lessard, Isabelle, Lavoie, Caroline, Côté, Isabelle, Mathieu, Jean
منشور في 2018نص -
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MRI-based Medical Nanorobotic Platform for the Control of Magnetic Nanoparticles and Flagellated Bacteria for Target Interventions in Human Capillaries حسب Martel, Sylvain, Felfoul, Ouajdi, Mathieu, Jean-Baptiste, Chanu, Arnaud, Tamaz, Samer, Mohammadi, Mahmood, Mankiewicz, Martin, Tabatabaei, Nasr
منشور في 2009نص -
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Towards an integrative approach to the management of myotonic dystrophy type 1 حسب Gagnon, Cynthia, Noreau, Luc, Moxley, Richard T, Laberge, Luc, Jean, Stéphane, Richer, Louis, Perron, Michel, Veillette, Suzanne, Mathieu, Jean
منشور في 2007نص -
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Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1 حسب Roussel, Marie-Pier, Morin, Marika, Girardin, Mélina, Fortin, Anne-Marie, Leone, Mario, Mathieu, Jean, Gagnon, Cynthia, Duchesne, Elise
منشور في 2019نص -
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High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses حسب Jilani, Abdulhakim, Matviychuk, Diana, Blaser, Susan, Dyack, Sarah, Mathieu, Jean, Prasad, Asuri N., Prasad, Chitra, Kyriakopoulou, Lianna, Mercimek‐Andrews, Saadet
منشور في 2019نص -
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The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care حسب De Antonio, Marie, Dogan, Céline, Daidj, Ferroudja, Eymard, Bruno, Puymirat, Jack, Mathieu, Jean, Gagnon, Cynthia, Katsahian, Sandrine, Hamroun, Dalil, Bassez, Guillaume
منشور في 2019نص -
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Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability حسب Bchetnia, Mbarka, Bouchard, Luigi, Mathieu, Jean, Campeau, Philippe M, Morin, Charles, Brisson, Diane, Laberge, Anne-Marie, Vézina, Hélène, Gaudet, Daniel, Laprise, Catherine
منشور في 2021نص -
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Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation حسب Tétreault, Martine, Gonzalez, Michael, Dicaire, Marie-Josée, Allard, Pierre, Gehring, Kalle, Leblanc, Diane, Leclerc, Nadine, Schondorf, Ronald, Mathieu, Jean, Zuchner, Stephan, Brais, Bernard
منشور في 2015نص -
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SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases حسب 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
منشور في 2016نص -
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Peripheral Nerve Stimulation Characteristics of an Asymmetric Head-Only Gradient Coil Compatible with a High-Channel-Count Receiver Array حسب 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.
منشور في 2015نص -
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Prevalence and determinants of hypertension and associated cardiovascular risk factors: data from a population-based, cross-sectional survey in Saint Louis, Senegal حسب 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
منشور في 2013نص -
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Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians حسب 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
منشور في 2020نص