Search Results - Couarch, Philippe

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  1. 1
    Homozygous TREM2 mutation in a family with atypical frontotemporal dementia

    Homozygous TREM2 mutation in a family with atypical frontotemporal dementia by Le Ber, Isabelle, De Septenville, Anne, Guerreiro, Rita, Bras, José, Camuzat, Agnès, Caroppo, Paola, Lattante, Serena, Couarch, Philippe, Kabashi, Edor, Bouya-Ahmed, Kawtar, Dubois, Bruno, Brice, Alexis

    Published in Neurobiology of aging
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  2. 2
    Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

    Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy by Chabrol, Elodie, Gourfinkel-An, Isabelle, Scheffer, Ingrid E, Picard, Fabienne, Couarch, Philippe, Berkovic, Samuel F, McMahon, Jacinta M, Bajaj, Nandita, Mota-Vieira, Luisa, Mota, Rui, Trouillard, Oriane, Depienne, Christel, Baulac, Michel, LeGuern, Eric, Baulac, Stéphanie

    Published in Epilepsy research
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  3. 3
    ELOVL5 Mutations Cause Spinocerebellar Ataxia 38

    ELOVL5 Mutations Cause Spinocerebellar Ataxia 38 by Di Gregorio, Eleonora, Borroni, Barbara, Giorgio, Elisa, Lacerenza, Daniela, Ferrero, Marta, Lo Buono, Nicola, Ragusa, Neftj, Mancini, Cecilia, Gaussen, Marion, Calcia, Alessandro, Mitro, Nico, Hoxha, Eriola, Mura, Isabella, Coviello, Domenico A., Moon, Young-Ah, Tesson, Christelle, Vaula, Giovanna, Couarch, Philippe, Orsi, Laura, Duregon, Eleonora, Papotti, Mauro Giulio, Deleuze, Jean-François, Imbert, Jean, Costanzi, Chiara, Padovani, Alessandro, Giunti, Paola, Maillet-Vioud, Marcel, Durr, Alexandra, Brice, Alexis, Tempia, Filippo, Funaro, Ada, Boccone, Loredana, Caruso, Donatella, Stevanin, Giovanni, Brusco, Alfredo

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  4. 4
    Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers

    Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers by Caroppo, Paola, Camuzat, Agnès, De Septenville, Anne, Couratier, Philippe, Lacomblez, Lucette, Auriacombe, Sophie, Flabeau, Olivier, Jornéa, Ludmila, Blanc, Frederic, Sellal, François, Cretin, Benjamin, Meininger, Vincent, Fleury, Marie-Céline, Couarch, Philippe, Dubois, Bruno, Brice, Alexis, Le Ber, Isabelle

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  5. 5
    Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism

    Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism by Couarch, Philippe, Vernia, Santiago, Gourfinkel-An, Isabelle, Lesca, Gaëtan, Gataullina, Svetlana, Fedirko, Estelle, Trouillard, Oriane, Depienne, Christel, Dulac, Olivier, Steschenko, Dominique, Leguern, Eric, Sanz, Pascual, Baulac, Stéphanie

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  6. 6
    A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22

    A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22 by Ouled Amar Ben Cheikh, Bouchra, Baulac, Stéphanie, Lahjouji, Fatiha, Bouhouche, Ahmed, Couarch, Philippe, Khalili, Naima, Regragui, Wafae, Lehericy, Stéphane, Ruberg, Merle, Benomar, Ali, Heath, Simon, Chkili, Taib, Yahyaoui, Mohamed, Jiddane, Mohamed, Ouazzani, Reda, LeGuern, Eric

    Published in Neurogenetics
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  7. 7
    Absence of mutations in the LGL1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy

    Absence of mutations in the LGL1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy by CHABROL, Elodie, GOURFINKEL -AN, Isabelle, TROUILLARD, Oriane, DEPIENNE, Christel, BAULAC, Michel, LEGUERN, Eric, BAULAC, Stephanie, SCHEFFER, Ingrid E, PICARD, Fabienne, COUARCH, Philippe, BERKOVIC, Samuel F, MCMAHON, Jacinta M, BAJAJ, Nandita, MOTA-VIEIRA, Luisa, MOTA, Rui

    Published in Epilepsy research
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