Comparative diagnosis interest of NfL and pNfH in CSF and plasma in a context of FTD–ALS spectrum von Escal, Jean, Fourier, Anthony, Formaglio, Maité, Zimmer, Luc, Bernard, Emilien, Mollion, Hélène, Bost, Muriel, Herrmann, Mathieu, Ollagnon-Roman, Elisabeth, Quadrio, Isabelle, Dorey, Jean-Michel

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Predictive testing for Huntington disease over 24 years: Evolution of the profile of the participants and analysis of symptoms von Ramond, Francis, Quadrio, Isabelle, Le Vavasseur, Laurence, Chaumet, Hélène, Boyer, Fabrice, Bost, Muriel, Ollagnon‐Roman, Elisabeth

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REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction von Goizet, Cyril, Depienne, Christel, Benard, Giovanni, Boukhris, Amir, Mundwiller, Emeline, Solé, Guilhem, Coupry, Isabelle, Pilliod, Julie, Martin-Négrier, Marie-Laure, Fedirko, Estelle, Forlani, Sylvie, Cazeneuve, Cécile, Hannequin, Didier, Charles, Perrine, Feki, Imed, Pinel, Jean-François, Ouvrard-Hernandez, Anne-Marie, Lyonnet, Stanislas, Ollagnon-Roman, Elisabeth, Yaouanq, Jacqueline, Toutain, Annick, Dussert, Christelle, Fontaine, Bertrand, Leguern, Eric, Lacombe, Didier, Durr, Alexandra, Rossignol, Rodrigue, Brice, Alexis, Stevanin, Giovanni

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Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues von Biancalana, Valérie, Scheidecker, Sophie, Miguet, Marguerite, Laquerrière, Annie, Romero, Norma B., Stojkovic, Tanya, Abath Neto, Osorio, Mercier, Sandra, Voermans, Nicol, Tanner, Laura, Rogers, Curtis, Ollagnon-Roman, Elisabeth, Roper, Helen, Boutte, Célia, Ben-Shachar, Shay, Lornage, Xavière, Vasli, Nasim, Schaefer, Elise, Laforet, Pascal, Pouget, Jean, Moerman, Alexandre, Pasquier, Laurent, Marcorelle, Pascale, Magot, Armelle, Küsters, Benno, Streichenberger, Nathalie, Tranchant, Christine, Dondaine, Nicolas, Schneider, Raphael, Gasnier, Claire, Calmels, Nadège, Kremer, Valérie, Nguyen, Karine, Perrier, Julie, Kamsteeg, Erik Jan, Carlier, Pierre, Carlier, Robert-Yves, Thompson, Julie, Boland, Anne, Deleuze, Jean-François, Fardeau, Michel, Zanoteli, Edmar, Eymard, Bruno, Laporte, Jocelyn

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Analysis of the DYSF mutational spectrum in a large cohort of patients von Krahn, Martin, Béroud, Christophe, Labelle, Véronique, Nguyen, Karine, Bernard, Rafaëlle, Bassez, Guillaume, Figarella-Branger, Dominique, Fernandez, Carla, Bouvenot, Julien, Richard, Isabelle, Ollagnon-Roman, Elisabeth, Bevilacqua, Jorge A, Salvo, Eric, Attarian, Shahram, Chapon, Françoise, Pellissier, Jean-François, Pouget, Jean, Hammouda, El Hadi, Laforêt, Pascal, Urtizberea, Jon Andoni, Eymard, Bruno, Leturcq, France, Lévy, Nicolas

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Motor and respiratory heterogeneity in Duchenne patients: Implication for clinical trials von Humbertclaude, Véronique, Hamroun, Dalil, Bezzou, Kamel, Bérard, Carole, Boespflug-Tanguy, Odile, Bommelaer, Christine, Campana-Salort, Emmanuelle, Cances, Claude, Chabrol, Brigitte, Commare, Marie-Christine, Cuisset, Jean-Marie, de Lattre, Capucine, Desnuelle, Claude, Echenne, Bernard, Halbert, Cécile, Jonquet, Olivier, Labarre-Vila, Annick, N’Guyen-Morel, Marie-Ange, Pages, Michel, Pepin, Jean-Louis, Petitjean, Thierry, Pouget, Jean, Ollagnon-Roman, Elisabeth, Richelme, Christian, Rivier, François, Sacconi, Sabrina, Tiffreau, Vincent, Vuillerot, Carole, Picot, Marie-Christine, Claustres, Mireille, Béroud, Christophe, Tuffery-Giraud, Sylvie

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Familial orbital myositis von Jacob, Maud, Ollagnon Roman, Elisabeth, Vighetto, Alain

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Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes von Coutelier, Marie, Hammer, Monia B, Stevanin, Giovanni, Monin, Marie-Lorraine, Davoine, Claire-Sophie, Mochel, Fanny, Labauge, Pierre, Ewenczyk, Claire, Ding, Jinhui, Gibbs, J. Raphael, Hannequin, Didier, Melki, Judith, Toutain, Annick, Laugel, Vincent, Forlani, Sylvie, Charles, Perrine, Broussolle, Emmanuel, Thobois, Stéphane, Afenjar, Alexandra, Anheim, Mathieu, Calvas, Patrick, Castelnovo, Giovanni, de Broucker, Thomas, Vidailhet, Marie, Moulignier, Antoine, Ghnassia, Robert T, Tallaksen, Chantal, Mignot, Cyril, Goizet, Cyril, Le Ber, Isabelle, Ollagnon-Roman, Elisabeth, Pouget, Jean, Brice, Alexis, Singleton, Andrew, Durr, Alexandra

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High intra-familiar clinical variability in MORC2 mutated CMT2 patients von Semplicini, Claudio, Ollagnon-Roman, Elisabeth, Leonard-Louis, Sarah, Piguet-Lacroix, Guenaelle, Silvestre, Manon, Latour, Philippe, Stojkovic, Tanya

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Comparative diagnosis interest of NfL and pNfH in CSF and plasma in a context of FTD–ALS spectrum von Escal, Jean, Fourier, Anthony, Formaglio, Maité, Zimmer, Luc, Bernard, Emilien, Mollion, Hélène, Bost, Muriel, Herrmann, Mathieu, Ollagnon-Roman, Elisabeth, Quadrio, Isabelle, Dorey, Jean-Michel

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Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7 von Coarelli, Giulia, Schule, Rebecca, van de Warrenburg, Bart P.C, De Jonghe, Peter, Ewenczyk, Claire, Martinuzzi, Andrea, Synofzik, Matthis, Hamer, Elisa G, Baets, Jonathan, Anheim, Mathieu, Schöls, Ludger, Deconinck, Tine, Masrori, Pegah, Fontaine, Bertrand, Klockgether, Thomas, DʼAngelo, Maria Grazia, Monin, Marie-Lorraine, De Bleecker, Jan, Migeotte, Isabelle, Charles, Perrine, Bassi, Maria Teresa, Klopstock, Thomas, Mochel, Fanny, Ollagnon-Roman, Elisabeth, DʼHooghe, Marc, Kamm, Christoph, Kurzwelly, Delia, Papin, Melanie, Davoine, Claire-Sophie, Banneau, Guillaume, Tezenas du Montcel, Sophie, Seilhean, Danielle, Brice, Alexis, Duyckaerts, Charles, Stevanin, Giovanni, Durr, Alexandra

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Overview of the WEEE Directive and Its Implementation in the Nordic Countries: National Realisations and Best Practices von Ylä-Mella, Jenni, Poikela, Kari, Lehtinen, Ulla, Tanskanen, Pia, Román, Elisabeth, Keiski, Riitta L., Pongrácz, Eva

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Biogas from Organic Waste - A Case Study von Mustafa, Mohamad Y., Calay, Rajnish K., Román, E.

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Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis von Bouton, Jean Marie, Neuhaus, Thomas, Aziza, Jacqueline, Makni, Saloua, Delezoide, Anne-Lise, Dijoud, Frédérique, Antignac, Corinne, Bouvier, Raymonde, Joubert, Madeleine, Roume, Joelle, Laube, Guido, Laurent, Nicole, Amar, Hatem Ben, Bieth, Eric, Gribouval, Olivier, Gubler, Marie Claire, Feuillet, François, Ollagnon-Roman, Elisabeth, Gonzales, Marie

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Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7 von Coarelli, Giulia, Schule, Rebecca, van de Warrenburg, Bart P.C, De Jonghe, Peter, Ewenczyk, Claire, Martinuzzi, Andrea, Synofzik, Matthis, Hamer, Elisa G, Baets, Jonathan, Anheim, Mathieu, Schoels, Ludger, Deconinck, Tine, Masrori, Pegah, Fontaine, Bertrand, Klockgether, Thomas, D'Angelo, Maria Grazia, Monin, Marie-Lorraine, De Bleecker, Jan, Migeotte, Isabelle, Charles, Perrine, Bassi, Maria Teresa, Klopstock, Thomas, Mochel, Fanny, Ollagnon-Roman, Elisabeth, D'Hooghe, Marc, Kamm, Christoph, Kurzwelly, Delia, Papin, Melanie, Davoine, Claire-Sophie, Banneau, Guillaume, du Montcel, Sophie Tezenas, Seilhean, Danielle, Brice, Alexis, Duyckaerts, Charles, Stevanin, Giovanni, Durr, Alexandra

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Congenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion von Jouaud, Maxime, Gonnaud, Pierre-Marie, Richard, Laurence, Latour, Philippe, Ollagnon-Roman, Elisabeth, Sturtz, Franck, Mathis, Stéphane, Magy, Laurent, Vallat, Jean-Michel

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Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds von Bauer, Peter, Stevanin, Giovanni, Beetz, Christian, Synofzik, Matthis, Schmitz-Hübsch, Tanja, Wüllner, Ullrich, Berthier, Eric, Ollagnon-Roman, Elisabeth, Riess, Olaf, Forlani, Sylvie, Mundwiller, Emeline, Durr, Alexandra, Schöls, Ludger, Brice, Alexis

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Analysis of the DYSF mutational spectrum in a large cohort of patients: DYSF Mutational Spectrum in a Large Cohort von Krahn, Martin, Béroud, Christophe, Labelle, Véronique, Nguyen, Karine, Bernard, Rafaëlle, Bassez, Guillaume, Figarella-Branger, Dominique, Fernandez, Carla, Bouvenot, Julien, Richard, Isabelle, Ollagnon-Roman, Elisabeth, Bevilacqua, Jorge A., Salvo, Eric, Attarian, Shahram, Chapon, Françoise, Pellissier, Jean-François, Pouget, Jean, Hammouda, El Hadi, Laforêt, Pascal, Urtizberea, Jon Andoni, Eymard, Bruno, Leturcq, France, Lévy, Nicolas

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a Value Chain Analysis For Bioenergy Production From Biomass and Biodegradable Waste : a Case Study in Northern Norway von Yu, Hao

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Migrationsforschung Als Kritik?: Konturen Einer Forschungsperspektive von Mecheril, Paul, Thomas-Olalde, Oscar, Melter, Claus, Arens, Susanne, Romaner, Elisabeth

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