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Your search keyword '"Hahn-Barma, Valérie"' showing total 26 results
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26 results on '"Hahn-Barma, Valérie"'

1. Identification of Atrophy Patterns in Alzheimer’s Disease Based on SVM Feature Selection and Anatomical Parcellation

Author

Mesrob, Lilia, Magnin, Benoit, Colliot, Olivier, Sarazin, Marie, Hahn-Barma, Valérie, Dubois, Bruno, Gallinari, Patrick, Lehéricy, Stéphane, Kinkingnéhun, Serge, Benali, Habib, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Doug, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Dohi, Takeyoshi, editor, Sakuma, Ichiro, editor, and Liao, Hongen, editor

Published
2008
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4. Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study

Author

Vidailhet, Marie, Vercueil, Laurent, Houeto, Jean-Luc, Krystkowiak, Pierre, Lagrange, Christelle, Yelnik, Jerôme, Bardinet, Eric, Benabid, Alim-Louis, Navarro, Soledad, Dormont, Didier, Grand, Sylvie, Blond, Serge, Ardouin, Claire, Pillon, Bernard, Dujardin, Katy, Hahn-Barma, Valérie, Agid, Yves, Destée, Alain, and Pollak, Pierre

Published
2007
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6. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

Author

Le Ber, Isabelle, Camuzat, Agnès, Hannequin, Didier, Pasquier, Florence, Guedj, Eric, Rovelet-Lecrux, Anne, Hahn-Barma, Valérie, van der Zee, Julie, Clot, Fabienne, Bakchine, Serge, Puel, Michèle, Ghanim, Mustapha, Lacomblez, Lucette, Mikol, Jacqueline, Deramecourt, Vincent, Lejeune, Pascal, de la Sayette, Vincent, Belliard, Serge, Vercelletto, Martine, Meyrignac, Christian, Van Broeckhoven, Christine, Lambert, Jean-Charles, Verpillat, Patrice, Campion, Dominique, Habert, Marie-Odile, Dubois, Bruno, and Brice, Alexis

Published
2008

13. La batterie d'évaluation des connaissances sémantiques du GRECO (BECS-GRECO) : validation et données normatives

Author

Merck, Catherine, primary, Charnallet, Annik, additional, Auriacombe, Sophie, additional, Belliard, Serge, additional, Hahn-Barma, Valérie, additional, Kremin, Helgard, additional, Lemesle, Béatrice, additional, Mahieux, Florence, additional, Moreaud, Olivier, additional, Palisson, Danièle Perrier, additional, Roussel, Martine, additional, Sellal, François, additional, and Siegwart, Hervine, additional

Published
2011
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14. P2-029: Similar beta-amyloid burden in posterior cortical atrophy and Alzheimer's disease

Author

de Souza, Leonardo, primary, Corlier, Fabian, additional, Habert, Marie Odile, additional, Uspenskaya, Olga, additional, Maroy, Renaud, additional, Lamari, Foudil, additional, Chupin, Marie, additional, Lehéricy, Stéphane, additional, Colliot, Olivier, additional, Hahn-Barma, Valérie, additional, Dubois, Bruno, additional, Bottlaender, Michel, additional, and Sarazin, Marie, additional

Published
2011
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20. Mental deficiency in three families with SPG4 spastic paraplegia.

Author

Ribaï, Pascale, Depienne, Christel, Fedirko, Estelle, Jothy, Anne-Catherine, Viveweger, Caterine, Hahn-Barma, Valérie, Brice, Alexis, and Durr, Alexandra

Subjects
GENETIC mutation, SPASTIC paralysis, PARAPLEGIA, EXTREMITIES (Anatomy), DEMENTIA, INTELLECTUAL disabilities
Abstract

Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP). Patients have pyramidal signs in the lower limbs and some present additional features including cognitive impairment such as executive dysfunction or subcortical dementia. We report 13 patients from three SPG4 families, who had spastic paraplegia associated with mental retardation (n=1), extensive social dependence (n=10), or isolated psychomotor delay (n=2). In family FSP-698, 10 affected individuals had both HSP and mental deficiency leading to social dependence in 9 and institutionalization in 5. The mean age at onset of spastic paraplegia was 11±20 years, ranging from 1 to 51 years. This phenotype segregated either with a novel p.Glu442Lys mutation or the two previously described p.Arg459Thr and p.Arg499Cys substitutions in the SPG4 gene. Since two of these mutations were previously reported in families with a pure form of the disease, another genetic factor linked to SPG4 could be responsible for this complex phenotype.European Journal of Human Genetics (2008) 16, 97–104; doi:10.1038/sj.ejhg.5201922; published online 24 October 2007 [ABSTRACT FROM AUTHOR]

Published
2008
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24. Homozygosity in Huntington's disease.

Author

Dx00DC;RR, ALEXANDRA, HAHN-BARMA, VALÉRIE, BRICE, ALEXIS, PÊCHEUX, CHRISTOPHE, DODÉ, CATHERINE, and FEINGOLD, JOSUÉ

Published
1999

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