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Co-authors
(313)
Alexis Brice
34
Didier Hannequin
20
Alexandra Durr (Alexandra Dürr)
18
Bruno Dubois
15
Lucette Lacomblez
12
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Authors
Isabelle Le Ber
Isabelle Le Ber,Pierre and Marie Curie University,Neuroscience,Genetics & Genealogy,Diseases
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Isabelle Le Ber
Pierre and Marie Curie University
Publications:
45
|
Citations:
554
Fields:
Neuroscience
,
Genetics & Genealogy
,
Diseases
View FAQ about top research areas and Fields of study
Collaborated with
313 co-authors
from 2003 to 2011
|
Cited by
2077 authors
Cumulative
Annual
Sort by:
Publications
(45)
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RefWorks
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Fronto-temporal lobar degeneration: neuropathology in 60 cases
Danielle Seilhean
,
Isabelle Le Ber
,
Marie Sarazin
,
Lucette Lacomblez
,
Stéphanie Millecamps
,
François Salachas
,
Pierre-François Pradat
,
Nadine Le Forestier
,
Eric LeGuern
,
Bruno Dubois
,
Vincent Meininger
,
Alexis Brice
http://academic.research.microsoft.com/io.ashx?type=5&id=48099609&selfId1=3697261&selfId2=0&maxNumber=12&query=
Journal:
Journal of Neural Transmission - J NEURAL TRANSM
, vol. 118, no. 5, pp. 753-764, 2011
Nosologie des dégénérescences lobaires frontotemporales
D. Hannequin
,
D. Wallon
,
O. Martinaud
,
D. Maltete
,
V. Deramecourt
,
D. Campion
,
I. Le Ber
Journal:
Pratique Neurologique - Fmc
, vol. 2, no. 2, pp. 53-63, 2011
Autosomal recessive cerebellar ataxias with oculomotor apraxia
Isabelle Le Ber
,
Alexandra Dürr
,
Alexis Brice
Journal:
Handbook of Clinical Neurology
, vol. 103, pp. 333-341, 2011
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
(
Citations: 11
)
Stéphanie Millecamps
,
François Salachas
,
Cécile Cazeneuve
,
Paul Gordon
,
Bernard Bricka
,
Agnès Camuzat
,
Léna Guillot-Noël
,
Odile Russaouen
,
Gaëlle Bruneteau
,
Pierre-François Pradat
,
Nadine Le Forestier
,
Nadia Vandenberghe
Isabelle Le Ber
http://academic.research.microsoft.com/io.ashx?type=5&id=30640745&selfId1=3697261&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 47, no. 8, pp. 554-560, 2010
CHMP2B mutations are rare in French families with frontotemporal lobar degeneration
(
Citations: 1
)
Mustapha Ghanim
,
Léna Guillot-Noel
,
Florence Pasquier
,
Ludmila Jornea
,
Vincent Deramecourt
,
Bruno Dubois
,
Isabelle Le Ber
,
Alexis Brice
Journal:
Journal of Neurology - J NEUROL
, vol. 257, no. 12, pp. 2032-2036, 2010
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Citations
(554 times by 416 publications)
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
Carlos Cruchaga
,
Sumitra Chakraverty
,
Kevin Mayo
,
Francesco L. M. Vallania
,
Robi D. Mitra
,
Kelley Faber
,
Jennifer Williamson
,
Tom Bird
,
Ramon Diaz-Arrastia
,
Tatiana M. Foroud
,
Bradley F. Boeve
,
Neill R. Graff-Radford
http://academic.research.microsoft.com/io.ashx?type=5&id=57402373&selfId1=3697261&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 2, 2012
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
(
Citations: 5
)
Justin P. Pearson
,
Nigel M. Williams
,
Elisa Majounie
,
Adrian Waite
,
Jennifer Stott
,
Victoria Newsway
,
Alex Murray
,
Dena Hernandez
,
Rita Guerreiro
,
Andrew B. Singleton
,
James Neal
,
Huw R. Morris
Journal:
Journal of Neurology - J NEUROL
, vol. 258, no. 4, pp. 647-655, 2011
Modelling the Effects of Penetrance and Family Size on Rates of Sporadic and Familial Disease
(
Citations: 1
)
Ammar Al-Chalabi
,
Cathryn M. Lewis
Journal:
Human Heredity - HUM HERED
, vol. 71, pp. 281-288, 2011
Combined Therapy with Idebenone and Deferiprone in Patients with Friedreich’s Ataxia
(
Citations: 3
)
Daniel Velasco-Sánchez
,
Asuncion Aracil
,
Raquel Montero
,
Ana Mas
,
Lorenzo Jiménez
,
Mar O’Callaghan
,
Maria Tondo
,
Antoni Capdevila
,
Josep Blanch
,
Rafael Artuch
,
Mercedes Pineda
Journal:
Cerebellum
, vol. 10, no. 1, pp. 1-8, 2011
A Comprehensive Review of Spinocerebellar Ataxia Type 2 in Cuba
(
Citations: 1
)
Luis Velázquez-Pérez
,
Roberto Rodríguez-Labrada
,
Julio Cesar García-Rodríguez
,
Luis Enrique Almaguer-Mederos
,
Tania Cruz-Mariño
,
José Miguel Laffita-Mesa
Journal:
Cerebellum
, vol. 10, no. 2, pp. 184-198, 2011
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