E-LIB Suche - Ergebnisse für: Hannequin, I.

1

Prolog: A new parallel evaluation scheme:

Hannequin, I. ; Goncalves, G. ; Lecouffe, P..
Microprocessing and Microprogramming. 27 (1989) 1-5 - p. 391-396 , 1989

Link: https://doi.org/10.1016/..

2

PP164-MON A NATIONAL OBSERVATIONAL SURVEY ON HEALTH CARE WO..:

Hébuterne, X. ; Durand, J. ; Antoun, S....
Clinical Nutrition Supplements. 6 (2011) 1 - p. 176 , 2011

Link: https://doi.org/10.1016/..

3

Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU..:

Liu, H. ; Li, J. ; Ziegemeier, E....
The Journal of Prevention of Alzheimer's Disease. , 2024

Link: https://doi.org/10.14283..

4

Étude descriptive de l'épilepsie dans les formes autosomiqu..:

Zarea, A. ; Pasquier, F. ; Pariente, J....
Revue Neurologique. 170 (2014) - p. A126 , 2014

Link: https://doi.org/10.1016/..

5

Génétique de la maladie d'Alzheimer sporadique avant 50ans:

Wallon, D. ; Rovelet-Lecrux, A. ; Pasquier, F....
Revue Neurologique. 170 (2014) - p. A196-A197 , 2014

Link: https://doi.org/10.1016/..

6

Genome-wide haplotype association study identifies the FRMD..:

EADI consortium, GERAD consortium ; Lambert, J-C ; Grenier-Boley, B...
Molecular Psychiatry. 18 (2012) 4 - p. 461-470 , 2012

Link: https://doi.org/10.1038/..

7

Frequency and Phenotypes Associated with C9ORF72 Repeat Exp..:

Le Ber, I. ; Camuzat, A. ; Guillot-Noel, L....
Neurology. 78 (2012) Meeting Abstracts 1 - p. S54.003-S54.003 , 2012

Link: https://doi.org/10.1212/..

8

Fréquence et phénotypes associés aux mutations du gène c9or..:

Le Ber, I. ; Camuzat, A. ; Hannequin, D....
Revue Neurologique. 168 (2012) - p. A196 , 2012

Link: https://doi.org/10.1016/..

9

O1-1 Etat actuel des investigations dans les formes monogén..:

Wallon, D. ; Jurici, S. ; Guyant-Maréchal, L....
Revue Neurologique. 165 (2009) 10 - p. 37 , 2009

Link: https://doi.org/10.1016/..

10

Chromosome 9p-linked families with frontotemporal dementia ..:

Le Ber, I. ; Camuzat, A. ; Berger, E....
Neurology. 72 (2009) 19 - p. 1669-1676 , 2009

Link: https://doi.org/10.1212/..

11

INTRAFAMILIAL DIVERSITY OF PHENOTYPE ASSOCIATED WITHAPPDUPL..:

Guyant-Marechal, I. ; Berger, E. ; Laquerrière, A....
Neurology. 71 (2008) 23 - p. 1925-1926 , 2008

Link: https://doi.org/10.1212/..

12

BRAIN SPECT PERFUSION OF FRONTOTEMPORAL DEMENTIA ASSOCIATED..:

Guedj, E. ; Ber, I. Le ; Lacomblez, L....
Neurology. 69 (2007) 5 - p. 488-490 , 2007

Link: https://doi.org/10.1212/..

13

Mutations du gène de la progranuline dans les démences fron..:

Le Ber, I. ; Camuzat, A. ; Hannequin, D....
Revue Neurologique. 163 (2007) 4 - p. 207-208 , 2007

Link: https://doi.org/10.1016/..

14

Valosin-containing protein gene mutations: Clinical and neu..:

Guyant-Maréchal, L. ; Laquerrière, A. ; Duyckaerts, C....
Neurology. 67 (2006) 4 - p. 644-651 , 2006

Link: https://doi.org/10.1212/..

15

Demographic, neurological and behavioural characteristics a..:

Ber, I. L. ; Guedj, E. ; Gabelle, A....
Brain. 129 (2006) 11 - p. 3051-3065 , 2006

Link: https://doi.org/10.1093/..