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Guillot-noel, L
281  results:
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1

Investigation of sex-specific effects of apolipoprotein E o..:

Schrewe, L. ; Lill, C. M. ; Liu, T....
Journal of Neuroinflammation.  12 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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2

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/..
 
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3

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/..
 
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4

Clinical and genetic keys to cerebellar ataxia due to FGF14..:

Méreaux, Jean-Loup ; Davoine, Claire-Sophie ; Pellerin, David...
eBioMedicine.  99 (2024)  - p. 104931 , 2024
Link: https://doi.org/10.1016/..
 
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5

Intermediate repeat expansions of TBP and STUB1: Genetic mo..:

Barbier, Mathieu ; Davoine, Claire-Sophie ; Petit, Emilien...
Genetics in Medicine.  25 (2023)  2 - p. 100327 , 2023
Link: https://doi.org/10.1016/..
 
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6

NPTX1 mutations trigger endoplasmic reticulum stress and ca..:

Coutelier, Marie ; Jacoupy, Maxime ; Janer, Alexandre...
Brain.  145 (2021)  4 - p. 1519-1534 , 2021
Link: https://doi.org/10.1093/..
 
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7

Biallelic loss-of-function variations in PRDX3 cause cerebe..:

Rebelo, Adriana P ; Eidhof, Ilse ; Cintra, Vivian P...
Brain.  144 (2021)  5 - p. 1467-1481 , 2021
Link: https://doi.org/10.1093/..
 
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8

Low-Frequency and Rare-Coding Variation Contributes to Mult..:

Mitrovič, Mitja ; Patsopoulos, Nikolaos A. ; Beecham, Ashley H....
Cell.  180 (2020)  2 - p. 403 , 2020
Link: https://doi.org/10.1016/..
 
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9

Low-Frequency and Rare-Coding Variation Contributes to Mult..:

Mitrovič, Mitja ; Patsopoulos, Nikolaos A. ; Beecham, Ashley H....
Cell.  178 (2019)  1 - p. 262 , 2019
Link: https://doi.org/10.1016/..
 
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10

Novel VCP mutations expand the mutational spectrum of front..:

Saracino, Dario ; Clot, Fabienne ; Camuzat, Agnès...
Neurobiology of Aging.  72 (2018)  - p. 187.e11-187.e14 , 2018
Link: https://doi.org/10.1016/..
 
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11

Low-Frequency and Rare-Coding Variation Contributes to Mult..:

Mitrovič, Mitja ; Patsopoulos, Nikolaos A. ; Beecham, Ashley H....
Cell.  175 (2018)  6 - p. 1679-1687.e7 , 2018
Link: https://doi.org/10.1016/..
 
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12

Adaptive human immunity drives remyelination in a mouse mod..:

El Behi, Mohamed ; Sanson, Charles ; Bachelin, Corinne...
Brain.  140 (2017)  4 - p. 967-980 , 2017
Link: https://doi.org/10.1093/..
 
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13

Energy level structure and optical dephasing under magnetic..:

Marino, Robert ; Lorgeré, Ivan ; Guillot-Noël, Olivier...
Journal of Luminescence.  169 (2016)  - p. 478-482 , 2016
Link: https://doi.org/10.1016/..
 
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14

Role of immune gene variants in multiple sclerosis suscepti..:

El Behi, Mohamed ; Damotte, Vincent ; Guillot-nöel, Lena...
Journal of Neuroimmunology.  275 (2014)  1-2 - p. 50 , 2014
Link: https://doi.org/10.1016/..
 
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15

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loc..:

International Multiple Sclerosis Genetics Consortium ; Lill, Christina M. ; Schjeide, Brit-Maren M....
Brain.  136 (2013)  6 - p. 1778-1782 , 2013
Link: https://doi.org/10.1093/..
 
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