| 000 | 01910 a2200589 4500 | ||
|---|---|---|---|
| 005 | 20250517014147.0 | ||
| 264 | 0 | _c20150928 | |
| 008 | 201509s 0 0 eng d | ||
| 022 | _a1878-5883 | ||
| 024 | 7 |
_a10.1016/j.jns.2015.01.008 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRoubertie, Agathe | |
| 245 | 0 | 0 |
_aNeuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction. _h[electronic resource] |
| 260 |
_bJournal of the neurological sciences _cFeb 2015 |
||
| 300 |
_a154-60 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAtrophy |
| 650 | 0 | 4 |
_aBrain _xpathology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGTP Phosphohydrolases _xgenetics |
| 650 | 0 | 4 |
_aHearing Loss _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xgenetics |
| 650 | 0 | 4 | _aMotor Activity |
| 650 | 0 | 4 | _aNeurologic Examination |
| 650 | 0 | 4 |
_aOptic Atrophy, Autosomal Dominant _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aLeboucq, Nicolas | |
| 700 | 1 | _aPicot, Marie Christine | |
| 700 | 1 | _aNogue, Erika | |
| 700 | 1 | _aBrunel, Hervé | |
| 700 | 1 | _aLe Bars, Emmanuelle | |
| 700 | 1 | _aManes, Gael | |
| 700 | 1 | _aAngebault Prouteau, Claire | |
| 700 | 1 | _aBlanchet, Catherine | |
| 700 | 1 | _aMondain, Michel | |
| 700 | 1 | _aChevassus, Hugues | |
| 700 | 1 | _aAmati-Bonneau, Patrizia | |
| 700 | 1 | _aSarzi, Emmanuelle | |
| 700 | 1 | _aPagès, Michel | |
| 700 | 1 | _aVillain, Max | |
| 700 | 1 | _aMeunier, Isabelle | |
| 700 | 1 | _aLenaers, Guy | |
| 700 | 1 | _aHamel, Christian P | |
| 773 | 0 |
_tJournal of the neurological sciences _gvol. 349 _gno. 1-2 _gp. 154-60 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.jns.2015.01.008 _zAvailable from publisher's website |
| 999 |
_c24584707 _d24584707 |
||