TY  - GEN
AU  - Roubertie,Agathe
AU  - Leboucq,Nicolas
AU  - Picot,Marie Christine
AU  - Nogue,Erika
AU  - Brunel,Hervé
AU  - Le Bars,Emmanuelle
AU  - Manes,Gael
AU  - Angebault Prouteau,Claire
AU  - Blanchet,Catherine
AU  - Mondain,Michel
AU  - Chevassus,Hugues
AU  - Amati-Bonneau,Patrizia
AU  - Sarzi,Emmanuelle
AU  - Pagès,Michel
AU  - Villain,Max
AU  - Meunier,Isabelle
AU  - Lenaers,Guy
AU  - Hamel,Christian P
TI  - Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction
SN  - 1878-5883
PY  - 2015///0928
KW  - Adolescent
KW  - Atrophy
KW  - Brain
KW  - pathology
KW  - Child
KW  - Child, Preschool
KW  - Female
KW  - GTP Phosphohydrolases
KW  - genetics
KW  - Hearing Loss
KW  - Humans
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Mitochondrial Diseases
KW  - Motor Activity
KW  - Neurologic Examination
KW  - Optic Atrophy, Autosomal Dominant
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.jns.2015.01.008
ER  -