Genetics of familial ALS and consequences for diagnosis von Camu, W, Khoris, J, Moulard, B, Salachas, F, Briolotti, V, Rouleau, G.A, Meininger, V

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Weight loss in Huntington disease increases with higher CAG repeat number von AZIZ, N. A, VAN DER BURG, J. M. M, LANDWEHRMEYER, G. B, BRUNDIN, P, STIJNEN, T, ROOS, R. A. C

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Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country von Khoris, J., Moulard, B., Briolotti, V., Hayer, M., Durieux, A., Clavelou, P., Malafosse, A., Rouleau, G. A., Camu, W.

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Disease severity and progression in progressive supranuclear palsy and multiple system atrophy: validation of the NNIPPS--Parkinson Plus Scale von Payan, Christine A M, Viallet, François, Landwehrmeyer, Bernhard G, Bonnet, Anne-Marie, Borg, Michel, Durif, Franck, Lacomblez, Lucette, Bloch, Frédéric, Verny, Marc, Fermanian, Jacques, Agid, Yves, Ludolph, Albert C, Leigh, Peter N, Bensimon, Gilbert

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SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist von CORCIA, P, KHORIS, J, COURATIER, P, MAYEUX-PORTAS, V, BIETH, E, DE TOFFOL, B, AUTRET, A, MÜH, J. P, ANDRES, C, CAMU, W

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How to Capitalize on the Retest Effect in Future Trials on Huntington's Disease von Schramm, Catherine, Katsahian, Sandrine, Youssov, Katia, Démonet, Jean-François, Krystkowiak, Pierre, Supiot, Frédéric, Verny, Christophe, Cleret de Langavant, Laurent, Bachoud-Lévi, Anne-Catherine

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Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis von Corcia, Philippe, Mayeux-Portas, Véronique, Khoris, Jawad, de Toffol, Bertrand, Autret, Alain, Müh, Jean-Pierre, Camu, William, Andres, Christian, the French ALS Research Group

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A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q von Hand, Collette K., Khoris, Jawad, Salachas, François, Gros-Louis, François, Lopes, Ana Amélia Simões, Mayeux-Portas, Veronique, Brown, Robert H., Meininger, Vincent, Camu, William, Rouleau, Guy A.

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Étude épidémiologique, phénotypique et génétique rétrospective dans une cohorte de 283 familles : un nouvel argument pour la prédominance d’une transmission non monogénique... von Corcia, P., Valdmanis, P., Khoris, J., Praline, J., Morales, C., Pageot, N., Vourc’h, P., Andres, C., Rouleau, G., Camu, W.

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Placebo effect characteristics observed in a single, international, longitudinal study in Huntington's disease von Cubo, Esther, González, Miguel, del Puerto, Inés, de Yébenes, Justo Garcia, Arconada, Olga Fernández, Gabriel y Galán, José María Trejo

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The economic costs of progressive supranuclear palsy and multiple system atrophy in France, Germany and the United Kingdom von McCrone, Paul, Payan, Christine Anne Mary, Knapp, Martin, Ludolph, Albert, Agid, Yves, Leigh, P Nigel, Bensimon, Gilbert

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Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family von Hand, Collette K., Mayeux-Portas, Veronique, Khoris, Jawad, Briolotti, Valerie, Clavelou, Pierre, Camu, William, Rouleau, Guy A.

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Absence of mutations in the hypoxia response element of VEGF in ALS von Gros-Louis, Francois, Laurent, Sandra, Lopes, Ana Amelia Simoes, Khoris, Jawad, Meininger, Vincent, Camu, William, Rouleau, Guy A.

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Genetics of familial ALS and consequences for diagnosis. French ALS Research Group von Camu, W, Khoris, J, Moulard, B, Salachas, F, Briolotti, V, Rouleau, G A, Meininger, V

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Plasmonic/magnetic molybdenum trioxide and graphitic carbon nitride quantum dots-based fluoroimmunosensing system for influenza virus von Achadu, Ojodomo J., Takemura, Kenshin, Khoris, Indra Memdi, Park, Enoch Y.

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Signal-amplified surface-enhanced Raman scattering using core/shell satellite nanoparticles for norovirus detection von Park, Enoch Y., Maehata, Syuei, Khoris, Indra Memdi, Achadu, Ojodomo J.

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Molybdenum Trioxide Quantum Dot-Encapsulated Nanogels for Virus Detection by Surface-Enhanced Raman Scattering on a 2D Substrate von Achadu, Ojodomo J, Abe, Fuyuki, Li, Tian-Cheng, Khoris, Indra Memdi, Lee, Dongkyu, Lee, Jaebeom, Suzuki, Tetsuro, Park, Enoch Y

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Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees von Parton, Matthew J., Andersen, Peter M., Broom, Wendy J., Shaw, Christopher E.

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