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Amati-Bonneau, P
269  results:
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1

Loss of function of Ywhah in mice induces deafness and coch..:

Buret, L ; Rebillard, G ; Brun, E...
Cell Death Discovery.  2 (2016)  1 - p. , 2016
Link: https://doi.org/10.1038/..
 
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2

Multiethnic involvement in autosomal-dominant optic atrophy..:

Loo, J L ; Singhal, S ; Rukmini, A V...
Eye.  31 (2016)  3 - p. 475-480 , 2016
Link: https://doi.org/10.1038/..
 
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3

The wide POLG-related spectrum: An integrated view:

Béreau, M. ; Anheim, M. ; Echaniz-Laguna, A....
Journal of the Neurological Sciences.  368 (2016)  - p. 70-76 , 2016
Link: https://doi.org/10.1016/..
 
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4

Mitochondrial dysfunction affecting visual pathways:

Leruez, S. ; Amati-Bonneau, P. ; Verny, C....
Revue Neurologique.  170 (2014)  5 - p. 344-354 , 2014
Link: https://doi.org/10.1016/..
 
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5

Mutations du gène OPA1 associant neuropathie optique et sur..:

Guillet-Pichon, V. ; Leruez, S. ; Milea, D....
Revue Neurologique.  170 (2014)  - p. A15 , 2014
Link: https://doi.org/10.1016/..
 
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6

Perspectives of drug-based neuroprotection targeting mitoch..:

Procaccio, V. ; Bris, C. ; Chao de la Barca, J.M....
Revue Neurologique.  170 (2014)  5 - p. 390-400 , 2014
Link: https://doi.org/10.1016/..
 
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7

Pathologie de la dynamique mitochondriale:

Amati-Bonneau, P. ; Chevrollier, A. ; Verny, C....
Revue Neurologique.  167 (2011)  - p. S10 , 2011
Link: https://doi.org/10.1016/..
 
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8

SimultaneousMFN2andGDAP1mutations cause major mitochondrial..:

Cassereau, J. ; Casasnovas, C. ; Gueguen, N....
Neurology.  76 (2011)  17 - p. 1524-1526 , 2011
Link: https://doi.org/10.1212/..
 
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9

Heterozygous OPA1 mutations in Behr syndrome:

Marelli, C. ; Amati-Bonneau, P. ; Reynier, P....
Brain.  134 (2010)  4 - p. e169-e169 , 2010
Link: https://doi.org/10.1093/..
 
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10

Les atrophies optiques héréditaires:

Scherer, C. ; Procaccio, V. ; Ferre, M....
Revue Neurologique.  166 (2010)  12 - p. 959-965 , 2010
Link: https://doi.org/10.1016/..
 
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11

Mitochondrial DNA A3243G mutation involved in familial diab..:

Verny, C. ; Amati-Bonneau, P. ; Letournel, F....
Diabetes & Metabolism.  34 (2008)  6 - p. 620-626 , 2008
Link: https://doi.org/10.1016/..
 
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12

MULTIPLE SCLEROSIS–LIKE DISORDER IN OPA1-RELATED AUTOSOMAL ..:

Verny, C. ; Loiseau, D. ; Scherer, C....
Neurology.  70 (2008)  13_part_2 - p. 1152-1153 , 2008
Link: https://doi.org/10.1212/..
 
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13

OPA1 mutations induce mitochondrial DNA instability and opt..:

Amati-Bonneau, P. ; Valentino, M. L. ; Reynier, P....
Brain.  131 (2008)  2 - p. 338-351 , 2008
Link: https://doi.org/10.1093/..
 
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14

A novel OPA1 mutation in a patient with severe, acute and l..:

NOCHEZ, Y ; ARSENE, S ; LE LEZ, ML...
Acta Ophthalmologica.  86 (2008)  - p. 0-0 , 2008
Link: https://doi.org/10.1111/..
 
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15

M - 16 Atrophie optique et atteinte neurologique avec mutat..:

Scherer, C. ; Verny, C. ; Lejeune, P....
Revue Neurologique.  163 (2007)  4 - p. 117 , 2007
Link: https://doi.org/10.1016/..
 
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