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hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes.
Isabelle Le Ber
,
Inge van Bortel
,
Gael Nicolas
,
Kawtar Bouya-Ahmed
,
Agnès Camuzat
,
et al.
Neurobiology of Aging, 2014, 35 (4), pp.934.e5-6
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hal-01245808v1
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C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing.
Isabelle Le Ber
,
Agnès Camuzat
,
Lena Guillot-Noel
,
Didier Hannequin
,
Lucette Lacomblez
,
et al.
Article dans une revue
hal-00924796v1
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FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.
Oriane Broustal
,
Agnès Camuzat
,
Lena Guillot-Noël
,
Nathalie Guy
,
Stéphanie Millecamps
,
et al.
Journal of Alzheimer's Disease, 2010, 22 (3), pp.765-9
Article dans une revue
hal-00926874v1
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Mutation in the 3’untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy
Gaël Nicolas
,
David Wallon
,
Claudia Goupil
,
Anne-Claire Richard
,
Cyril Pottier
,
et al.
Article dans une revue
hal-01234142v1
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Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the société Francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)
Laurent Gilardin
,
Sandrine Delignat
,
Ivan Peyron
,
Mathieu Ing
,
Yu-Chun Lone
,
et al.
Article dans une revue
hal-02466291v1
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Troubles de l’humeur : quand recourir à la stimulation magnétique transcrânienne ?
Samuel Bulteau
,
Charline Guirette
,
Jérôme Brunelin
,
Emmanuel Poulet
,
Benoit Trojak
,
et al.
Article dans une revue
hal-02160324v1
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Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders.
Serena Lattante
,
Stéphanie Millecamps
,
Giovanni Stevanin
,
Sophie Rivaud-Péchoux
,
Carine Moigneu
,
et al.
Neurology, 2014, 83 (11), pp.990-5
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hal-01205502v1
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