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Mouzat, K.
32
results:
Search for persons
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Format
Online (32)
Mediatypes
Articles (Online) (8)
OpenAccess-fulltext (24)
Languages
english (30)
french (1)
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1
French National Protocol for genetic of amyotrophic lateral..:
Corcia, P.
;
Vourc'h, P.
;
Bernard, E.
...
Revue Neurologique. 179 (2023) 9 - p. 1020-1029 , 2023
Link:
https://doi.org/10.1016/..
?
2
Pre-symptomatic diagnosis in ALS:
Corcia, P.
;
Lumbroso, S.
;
Cazeneuve, C.
...
Revue Neurologique. 176 (2020) 3 - p. 166-169 , 2020
Link:
https://doi.org/10.1016/..
?
3
Amyotrophic lateral sclerosis in Huntington disease gene ca..:
Bernard, E.
;
Mouzat, K.
;
Leblanc, P.
...
Revue Neurologique. 173 (2017) 10 - p. 670-671 , 2017
Link:
https://doi.org/10.1016/..
?
4
A novel autosomal dominant leukodystrophy with specific MRI..:
Corlobé, A.
;
Taithe, F.
;
Clavelou, P.
...
Journal of Neurology. 262 (2015) 4 - p. 988-991 , 2015
Link:
https://doi.org/10.1007/..
?
5
Phenotype and genotype analysis in amyotrophic lateral scle..:
Corcia, P.
;
Valdmanis, P.
;
Millecamps, S.
...
Neurology. 78 (2012) 19 - p. 1519-1526 , 2012
Link:
https://doi.org/10.1212/..
?
6
P.38 Genetic variability of LXRbeta gene might contribute t..:
Mouzat, K.
;
Mercier, E.
;
Polge, A.
...
Thrombosis Research. 127 (2011) - p. S138 , 2011
Link:
https://doi.org/10.1016/..
?
7
837 PROTEOMICS AND GENOMICS INVESTIGATIONS OF DIETHYLSTILBE..:
Bigot, P.
;
Mouzat, K.
;
Bourreau, A.
...
European Urology Supplements. 10 (2011) 2 - p. 265 , 2011
Link:
https://doi.org/10.1016/..
?
8
CO22 - Le récepteur nucléaire des oxystérols lxrbêta régule..:
Mouzat, K.
;
Prod'homme, M.
;
Volle, D.H.
...
Annales d'Endocrinologie. 67 (2006) 5 - p. 390 , 2006
Link:
https://doi.org/10.1016/..
?
9
Association of Variants in the SPTLC1 Gene with Juvenile Am..:
Johnson J. O
;
Chia R
;
Miller D. E
...
info:eu-repo/semantics/altIdentifier/pmid/34459874. , 2021
Link:
https://hdl.handle.net/1..
?
10
Association of variants in the SPTLC1 gene with juvenile am..:
Johnson, JO
;
Chia, R
;
Miller, DE
...
https://eprints.whiterose.ac.uk/180985/1/jamaneurology_johnson_2021_oi_210047_1633018740.39649.pdf. , 2021
Link:
https://eprints.whiteros..
?
11
Association of Variants in the SPTLC1 Gene with Juvenile Am..:
Johnson J. O
;
Chia R
;
Miller D. E
...
info:eu-repo/semantics/altIdentifier/pmid/34459874. , 2021
Link:
http://hdl.handle.net/11..
?
12
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
13
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres‐Ciga, S
;
Noyce, AJ
;
Hemani, G
...
https://eprints.whiterose.ac.uk/166378/7/ana.25431.pdf. , 2019
Link:
https://eprints.whiteros..
?
14
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
?
15
Shared polygenic risk and causal inferences in amyotrophic ..:
Bandres-Ciga S
;
Noyce A. J
;
Hemani G
...
info:eu-repo/semantics/altIdentifier/pmid/30723964. , 2019
Link:
http://hdl.handle.net/11..
1-15