GROMMET von DESJARDINS, Mathieu, BRAIS, Sylvain

Volltext bestellen

GROMMET von DESJARDINS, Mathieu, BRAIS, Sylvain

Volltext bestellen

GROMMET von BRAIS, SYLVAIN, DESJARDINS, MATHIEU

Volltext bestellen

GROMMET von DESJARDINS, Mathieu, BRAIS, Sylvain

Volltext bestellen

GROMMET von DESJARDINS MATHIEU, BRAIS SYLVAIN

Volltext bestellen

Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing von Perrier, Stefanie, Guerrero, Kether, Tran, Luan T, Michell-Robinson, Mackenzie A, Legault, Geneviève, Brais, Bernard, Sylvain, Michel, Dorman, James, Demos, Michelle, Köhler, Wolfgang, Pastinen, Tomi, Thiffault, Isabelle, Bernard, Geneviève

Volltext

Morphometric and Microstructural Changes During Murine Retinal Development Characterized Using In Vivo Optical Coherence Tomography von Brais-Brunet, Simon, Heckel, Émilie, Kanniyappan, Udayakumar, Chemtob, Sylvain, Boudoux, Caroline, Joyal, Jean-Sébastien, Dehaes, Mathieu

Volltext

Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations von Wolf, Nicole I, Vanderver, Adeline, van Spaendonk, Rosalina M.L, Schiffmann, Raphael, Brais, Bernard, Bugiani, Marianna, Sistermans, Erik, Catsman-Berrevoets, Coriene, Kros, Johan M, Pinto, Pedro Soares, Pohl, Daniela, Tirupathi, Sandya, Strømme, Petter, de Grauw, Ton, Fribourg, Sébastien, Demos, Michelle, Pizzino, Amy, Naidu, Sakkubai, Guerrero, Kether, van der Knaap, Marjo S, Bernard, Geneviève

Volltext

Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study von Dermer, E., Spahr, A., Tran, L. T., Mirchi, A., Pelletier, F., Guerrero, K., Ahmed, S., Brais, B., Braverman, N., Buhas, D., Chandratre, S., Chenier, S., Chrestian, N., Desmeules, M., Dilenge, M. E., Laflamme, J., Larbrisseau, A., Legault, G., Lim, K. Y., Maftei, C., Major, P., Malvey-Dorn, E., Marois, P., Mitchell, J., Nadeau, A., Osterman, B., Paradis, I., Pohl, D., Reggin, J., Riou, E., Roedde, G., Rossignol, E., Sébire, G., Shevell, M., Srour, M., Sylvain, M., Tarnopolsky, M., Venkateswaran, S., Sullivan, M., Bernard, G.

Volltext

3T MRI study discloses high intrafamilial variability in CADASIL due to a novel NOTCH3 mutation von La Piana, Roberta, Leppert, Ilana R., Pike, G. Bruce, Lanthier, Sylvain, Brais, Bernard, Tampieri, Donatella

Volltext

Characterization of a novel SPG3A deletion in a French-Canadian family von Meijer, Inge A., Dion, Patrick, Laurent, Sandra, Dupré, Nicolas, Brais, Bernard, Levert, Annie, Puymirat, Jacques, Rioux, Marie France, Sylvain, Michel, Zhu, Peng-Peng, Soderblom, Cynthia, Stadler, Julia, Blackstone, Craig, Rouleau, Guy A.

Volltext

Tremor–ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3–10q23.31 von Bernard, Geneviève, Thiffault, Isabelle, Tetreault, Martine, Putorti, Maria Lisa, Bouchard, Isabelle, Sylvain, Michel, Melançon, Serge, Laframboise, Rachel, Langevin, Pierre, Bouchard, Jean-Pierre, Vanasse, Michel, Vanderver, Adeline, Sébire, Guillaume, Brais, Bernard

Volltext

TACH Leukodystrophy: Locus Refinement to Chromosome 10q22.3-23.1 von Tétreault, Martine, Putorti, Maria Lisa, Thiffault, Isabelle, Sylvain, Michel, Venderver, Adeline, Schiffmann, Raphael, Brais, Bernard, Bernard, Geneviève

Volltext