Expanding the Spectrum of AP5Z1‐Related Hereditary Spastic Paraplegia (HSP‐SPG48): A Multicenter Study on a Rare Disease
Breza, Marianthi, Hirst, Jennifer, Chelban, Viorica, Banneau, Guillaume, Tissier, Laurène, Kol, Bophara, Bourinaris, Thomas, Said, Samia A., Péréon, Yann, Heinzmann, Anna, Debs, Rabab, Juntas‐Morales, Raul, Martinez, Victoria G., Camdessanche, Jean P., Scherer‐Gagou, Clarisse, Zola, Jean‐Médard, Athanasiou‐Fragkouli, Alkyoni, Efthymiou, Stephanie, Vavougios, George, Velonakis, Georgios, Stamelou, Maria, Tzartos, John, Potagas, Constantin, Zambelis, Thomas, Mariotti, Caterina, Blackstone, Craig, Vandrovcova, Jana, Mavridis, Theodoros, Kartanou, Chrisoula, Stefanis, Leonidas, Wood, Nicholas, Karadima, Georgia, LeGuern, Eric, Koutsis, Georgios, Houlden, Henry, Stevanin, Giovanni
Published in Movement disorders (01.04.2021)
Published in Movement disorders (01.04.2021)
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International Guidelines for the Treatment of Huntington's Disease
Bachoud-Lévi, Anne-Catherine, Ferreira, Joaquim, Massart, Renaud, Youssov, Katia, Rosser, Anne, Busse, Monica, Craufurd, David, Reilmann, Ralf, De Michele, Giuseppe, Rae, Daniela, Squitieri, Ferdinando, Seppi, Klaus, Perrine, Charles, Scherer-Gagou, Clarisse, Audrey, Olivier, Verny, Christophe, Burgunder, Jean-Marc
Published in Frontiers in neurology (2019)
Published in Frontiers in neurology (2019)
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Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseases
Journe‐Mallet, Isabelle, Gouju, Julien, Etcharry‐Bouyx, Frédérique, Chauvire, Valérie, Guillet‐Pichon, Virginie, Scherer‐Gagou, Clarisse, Prundean, Adriana, Godard, Sophie, Lecluse, Aldéric, Cassereau, Julien, Verny, Christophe, Letournel, Franck, Codron, Philippe
Published in Brain pathology (Zurich, Switzerland) (01.05.2023)
Published in Brain pathology (Zurich, Switzerland) (01.05.2023)
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Frequency and characteristics of short versus longitudinally extensive myelitis in adults with MOG antibodies: A retrospective multicentric study
Ciron, Jonathan, Cobo-Calvo, Alvaro, Audoin, Bertrand, Bourre, Bertrand, Brassat, David, Cohen, Mikael, Collongues, Nicolas, Deschamps, Romain, Durand-Dubief, Françoise, Laplaud, David, Maillart, Elisabeth, Papeix, Caroline, Zephir, Hélène, Bereau, Matthieu, Brochet, Bruno, Carra-Dallière, Clarisse, Derache, Nathalie, Gagou-Scherer, Clarisse, Henry, Carole, Kerschen, Philippe, Mathey, Guillaume, Maubeuge, Nicolas, Maurousset, Aude, Montcuquet, Alexis, Moreau, Thibault, Prat, Christophe, Taithe, Frédéric, Thouvenot, Eric, Tourbah, Ayman, Rollot, Fabien, Vukusic, Sandra, Marignier, Romain
Published in Multiple sclerosis (01.07.2020)
Published in Multiple sclerosis (01.07.2020)
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Evidence of mosaicism in SPAST variant carriers in four French families
Angelini, Chloé, Goizet, Cyril, Said, Samia Ait, Camu, William, Depienne, Christel, Heron, Bénédicte, Kol, Bophara, Guillaud-Bataille, Marine, Pennamen, Perrine, Rooryck, Caroline, Scherer-Gagou, Clarisse, Tissier, Laurène, Stevanin, Giovanni, Leguern, Eric, Banneau, Guillaume
Published in European journal of human genetics : EJHG (01.07.2021)
Published in European journal of human genetics : EJHG (01.07.2021)
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Human Fetal Cell Therapy in Huntington's Disease: A Randomized, Multicenter, Phase II Trial
Bachoud‐Lévi, Anne‐Catherine, Schramm, Catherine, Remy, Philippe, Aubin, Ghislaine, Blond, Serge, Bocket, Laurence, Brugières, Pierre, Calvas, Fabienne, Calvier, Elisabeth, Cassim, François, Challine, Dominique, Gagou, Clarisse Scherer, Langavant, Laurent Cleret, Collier, Francis, Cottencin, Olivier, David, Philippe, Damier, Philippe, Delliaux, Marie, Delmaire, Christine, Delval, Arnaud, Démonet, Jean‐François, Descamps, Philippe, Gaura, Véronique, Gohier, Bénédicte, Goldman, Serge, Haddad, Bassam, Izopet, Jacques, Jeny, Roland, Kerr‐Conte, Julie, Krystowiak, Pierre, Lalanne, Christophe, Lavisse, Sonia, Lefaucheur, Jean‐Pascal, Lemoine, Laurie, Levivier, Marc, Lotterie, Jean‐Albert, Lunel‐Fabiani, Françoise, Maison, Patrick, Massager, Nicolas, Massart, Renaud, Menei, Philippe, Montero‐Menei, Claudia, Neveu, Isabelle, Parant, Olivier, Pautot, Vivien, Payoux, Pierre, Pereon, Yann, Rialland, Amandine, Rosser, Anne, Rouard, Hélène, Schmitz, David, Simonetta‐Moreau, Marion, Simonin, Clémence, Slama, Hichem, Sol, Jean‐Christophe, Supiot, Frédéric, Tanguy, Jean‐Yves, Tenenbaum, Liliane, Verny, Christophe, Youssov, Katia, Peschanski, Marc, Audureau, Etienne, Palfi, Stéphane, Hantraye, Philippe
Published in Movement disorders (01.08.2020)
Published in Movement disorders (01.08.2020)
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IRF2BPL Causes Mild Intellectual Disability Followed by Late-Onset Ataxia
Heide, Solveig, Davoine, Claire-Sophie, Cunha, Paulina, Scherer-Gagou, Clarisse, Keren, Boris, Stevanin, Giovanni, Charles, Perrine, Heron, Delphine, Brice, Alexis, Durr, Alexandra
Published in Neurology. Genetics (01.12.2023)
Published in Neurology. Genetics (01.12.2023)
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Specific cognitive theory of mind and behavioral dysfunctions in early manifest Huntington disease: a case report
Caillaud, Marie, Laisney, Mickael, Bejanin, Alexandre, Scherer-Gagou, Clarisse, Bonneau, Dominique, Duclos, Harmony, Eustache, Francis, Verny, Christophe, Desgranges, Béatrice, Allain, Philippe
Published in Neurocase (02.01.2020)
Published in Neurocase (02.01.2020)
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Cognitive decline in Huntington's disease expansion gene carriers
Baake, Verena, Reijntjes, Robert H.A.M., Dumas, Eve M., Thompson, Jennifer C., Roos, Raymund A.C.
Published in Cortex (01.10.2017)
Published in Cortex (01.10.2017)
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Is multidetector CT-scan able to detect T3a renal tumor before surgery?
Renard, Anne Sophie, Nedelcu, Cosmina, Paisant, Anita, Saulnier, Patrick, Le Bigot, Jérôme, Azzouzi, Abdel Rahmene, Bigot, Pierre, Aubé, Christophe
Published in Scandinavian journal of urology (03.09.2019)
Published in Scandinavian journal of urology (03.09.2019)
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Syndrome de Brown-Séquard révélant un infarctus médullaire secondaire à une dissection vertébrale
Hoguin, Graziella, Le Verger, Léna, Scherer-Gagou, Clarisse, Godard, Sophie, Lecluse, Aldéric, Labriffe, Matthieu, Verny, Christophe
Published in Revue neurologique (01.03.2017)
Published in Revue neurologique (01.03.2017)
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Nouvelle mutation du gène WFS1 responsable d’un syndrome de Wolfram atypique de transmission autosomique dominante
Prundean, Adriana, Barth, Magalie, Paquis-Flucklinger, Veronique, Scherer-Gagou, Clarisse, Procaccio, Vincent, Bonneau, Dominique, Verny, Christophe
Published in Revue neurologique (01.04.2012)
Published in Revue neurologique (01.04.2012)
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