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21.
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Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers. [electronic resource] by
- Wallon, David
- Rovelet-Lecrux, Anne
- Deramecourt, Vincent
- Pariente, Jeremie
- Auriacombe, Sophie
- Le Ber, Isabelle
- Schraen, Suzanna
- Pasquier, Florence
- Campion, Dominique
- Hannequin, Didier
Producer: 20130220
In:
Journal of Alzheimer's disease : JAD vol. 32
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22.
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New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers. [electronic resource] by
- Viodé, Arthur
- Fournier, Clémence
- Camuzat, Agnès
- Fenaille, François
- Latouche, Morwena
- Elahi, Fanny
- Le Ber, Isabelle
- Junot, Christophe
- Lamari, Foudil
- Anquetil, Vincent
- Becher, François
Publication details: Frontiers in neuroscience 2018
In:
Frontiers in neuroscience vol. 12
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23.
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Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia. [electronic resource] by
- Le Ber, Isabelle
- Camuzat, Agnès
- Castelnovo, Giovanni
- Azulay, Jean-Philippe
- Genton, Pierre
- Gastaut, Jean-Louis
- Broglin, Dominique
- Labauge, Pierre
- Brice, Alexis
- Durr, Alexandra
Producer: 20030916
In:
Archives of neurology vol. 60
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24.
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TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia. [electronic resource] by
- Lattante, Serena
- Le Ber, Isabelle
- Camuzat, Agnès
- Dayan, Sarah
- Godard, Chloé
- Van Bortel, Inge
- De Septenville, Anne
- Ciura, Sorana
- Brice, Alexis
- Kabashi, Edor
Producer: 20140325
In:
Neurobiology of aging vol. 34
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25.
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Is hippocampal volume a good marker to differentiate Alzheimer's disease from frontotemporal dementia? [electronic resource] by
- de Souza, Leonardo Cruz
- Chupin, Marie
- Bertoux, Maxime
- Lehéricy, Stéphane
- Dubois, Bruno
- Lamari, Foudil
- Le Ber, Isabelle
- Bottlaender, Michel
- Colliot, Olivier
- Sarazin, Marie
Producer: 20131209
In:
Journal of Alzheimer's disease : JAD vol. 36
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26.
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FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. [electronic resource] by
- Biancalana, Valérie
- Toft, Mathias
- Le Ber, Isabelle
- Tison, François
- Scherrer, Elisabeth
- Thibodeau, Stephen
- Mandel, Jean Louis
- Brice, Alexis
- Farrer, Matthew J
- Dürr, Alexandra
Producer: 20050630
In:
Archives of neurology vol. 62
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27.
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Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients. [electronic resource] by
- Millecamps, Stéphanie
- De Septenville, Anne
- Teyssou, Elisa
- Daniau, Mailys
- Camuzat, Agnès
- Albert, Mélanie
- LeGuern, Eric
- Galimberti, Daniela
- Brice, Alexis
- Marie, Yannick
- Le Ber, Isabelle
Producer: 20151109
In:
Neurobiology of aging vol. 35
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28.
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Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. [electronic resource] by
- Lattante, Serena
- Le Ber, Isabelle
- Galimberti, Daniela
- Serpente, Maria
- Rivaud-Péchoux, Sophie
- Camuzat, Agnès
- Clot, Fabienne
- Fenoglio, Chiara
- Scarpini, Elio
- Brice, Alexis
- Kabashi, Edor
Producer: 20151019
In:
Neurobiology of aging vol. 35
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29.
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Increased prevalence of granulovacuolar degeneration in C9orf72 mutation. [electronic resource] by
- Riku, Yuichi
- Duyckaerts, Charles
- Boluda, Susana
- Plu, Isabelle
- Le Ber, Isabelle
- Millecamps, Stéphanie
- Salachas, François
- Yoshida, Mari
- Ando, Takashi
- Katsuno, Masahisa
- Sobue, Gen
- Seilhean, Danielle
Producer: 20200915
In:
Acta neuropathologica vol. 138
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30.
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Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. [electronic resource] by
- Rovelet-Lecrux, Anne
- Deramecourt, Vincent
- Legallic, Solenn
- Maurage, Claude-Alain
- Le Ber, Isabelle
- Brice, Alexis
- Lambert, Jean-Charles
- Frébourg, Thierry
- Hannequin, Didier
- Pasquier, Florence
- Campion, Dominique
Producer: 20080729
In:
Neurobiology of disease vol. 31
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31.
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Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin. [electronic resource] by
- Caroppo, Paola
- Le Ber, Isabelle
- Camuzat, Agnès
- Clot, Fabienne
- Naccache, Lionel
- Lamari, Foudil
- De Septenville, Anne
- Bertrand, Anne
- Belliard, Serge
- Hannequin, Didier
- Colliot, Olivier
- Brice, Alexis
Producer: 20150306
In:
JAMA neurology vol. 71
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32.
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A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations. [electronic resource] by
- Coppola, Cinzia
- Saracino, Dario
- Puoti, Gianfranco
- Lus, Giacomo
- Dato, Clemente
- Le Ber, Isabelle
- Pariente, Jeremie
- Caroppo, Paola
- Piccoli, Elena
- Tagliavini, Fabrizio
- Di Iorio, Giuseppe
- Rossi, Giacomina
Producer: 20171116
In:
Neurobiology of aging vol. 49
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33.
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Posterior cortical atrophy as an extreme phenotype of GRN mutations. [electronic resource] by
- Caroppo, Paola
- Belin, Catherine
- Grabli, David
- Maillet, Didier
- De Septenville, Anne
- Migliaccio, Raffaella
- Clot, Fabienne
- Lamari, Foudil
- Camuzat, Agnès
- Brice, Alexis
- Dubois, Bruno
- Le Ber, Isabelle
Producer: 20150415
In:
JAMA neurology vol. 72
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34.
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Homozygous TREM2 mutation in a family with atypical frontotemporal dementia. [electronic resource] 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
Producer: 20150209
In:
Neurobiology of aging vol. 35
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35.
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Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389R. [electronic resource] by
- Chaunu, Marie-Pierre
- Deramecourt, Vincent
- Buée-Scherrer, Valérie
- Le Ber, Isabelle
- Brice, Alexis
- Ehrle, Nathalie
- El Hachimi, Khalid
- Pluot, Michel
- Maurage, Claude-Alain
- Bakchine, Serge
- Buée, Luc
Producer: 20140713
In:
Journal of Alzheimer's disease : JAD vol. 37
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36.
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C9orf72 repeat expansions are a rare genetic cause of parkinsonism. [electronic resource] by
- Lesage, Suzanne
- Le Ber, Isabelle
- Condroyer, Christel
- Broussolle, Emmanuel
- Gabelle, Audrey
- Thobois, Stéphane
- Pasquier, Florence
- Mondon, Karl
- Dion, Patrick A
- Rochefort, Daniel
- Rouleau, Guy A
- Dürr, Alexandra
- Brice, Alexis
Producer: 20130410
In:
Brain : a journal of neurology vol. 136
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37.
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Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up. [electronic resource] by
- Ribaï, Pascale
- Pousset, Françoise
- Tanguy, Marie-Laure
- Rivaud-Pechoux, Sophie
- Le Ber, Isabelle
- Gasparini, Franchesca
- Charles, Perrine
- Béraud, Anne-Sophie
- Schmitt, Michele
- Koenig, Michel
- Mallet, Alain
- Brice, Alexis
- Dürr, Alexandra
Producer: 20070521
In:
Archives of neurology vol. 64
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38.
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Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substrates. [electronic resource] by
- Bartolome, Fernando
- Esteras, Noemi
- Martin-Requero, Angeles
- Boutoleau-Bretonniere, Claire
- Vercelletto, Martine
- Gabelle, Audrey
- Le Ber, Isabelle
- Honda, Tadashi
- Dinkova-Kostova, Albena T
- Hardy, John
- Carro, Eva
- Abramov, Andrey Y
Producer: 20181211
In:
Scientific reports vol. 7
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39.
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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. [electronic resource] by
- Chaussenot, Annabelle
- Le Ber, Isabelle
- Ait-El-Mkadem, Samira
- Camuzat, Agnès
- de Septenville, Anne
- Bannwarth, Sylvie
- Genin, Emmanuelle C
- Serre, Valérie
- Augé, Gaëlle
- Brice, Alexis
- Pouget, Jean
- Paquis-Flucklinger, Véronique
Producer: 20151109
In:
Neurobiology of aging vol. 35
Availability: No items available.
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40.
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hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. [electronic resource] by
- Le Ber, Isabelle
- Van Bortel, Inge
- Nicolas, Gael
- Bouya-Ahmed, Kawtar
- Camuzat, Agnès
- Wallon, David
- De Septenville, Anne
- Latouche, Morwena
- Lattante, Serena
- Kabashi, Edor
- Jornea, Ludmila
- Hannequin, Didier
- Brice, Alexis
Producer: 20140929
In:
Neurobiology of aging vol. 35
Availability: No items available.
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