|
|
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
|
Partager
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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
Article dans une revue
hal-01245808v1
|
Partager
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
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
|
Partager
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
I. Le Ber
,
A. Camuzat
,
Eric Berger
,
D. Hannequin
,
A. Laquerrière
,
et al.
Article dans une revue
hal-00408053v1
|
Partager
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.
Lina Benajiba
,
Isabelle Le Ber
,
Agnès Camuzat
,
Mathieu Lacoste
,
Catherine Thomas-Anterion
,
et al.
Article dans une revue
istex
hal-00407819v1
|
Partager
Gmail
Facebook
Twitter
LinkedIn
More
|