E-LIB Suche - Ergebnisse für: Mouzat, K.

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

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/..

7

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/..

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: http://hdl.handle.net/11..

10

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..

11

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..

12

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..

13

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..

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..