000 | 01892 a2200565 4500 | ||
---|---|---|---|
005 | 20250517181717.0 | ||
264 | 0 | _c20171208 | |
008 | 201712s 0 0 eng d | ||
022 | _a1471-2415 | ||
024 | 7 |
_a10.1186/s12886-017-0583-3 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMashima, Yukihiko | |
245 | 0 | 0 |
_aVisual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation. _h[electronic resource] |
260 |
_bBMC ophthalmology _cOct 2017 |
||
300 |
_a192 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAge of Onset |
650 | 0 | 4 | _aAged |
650 | 0 | 4 |
_aAntioxidants _xtherapeutic use |
650 | 0 | 4 |
_aAscorbic Acid _xtherapeutic use |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aFollow-Up Studies |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 |
_aOptic Atrophy, Hereditary, Leber _xdrug therapy |
650 | 0 | 4 | _aPoint Mutation |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 | _aPrognosis |
650 | 0 | 4 |
_aRecovery of Function _xphysiology |
650 | 0 | 4 | _aRetrospective Studies |
650 | 0 | 4 |
_aRiboflavin _xtherapeutic use |
650 | 0 | 4 |
_aUbiquinone _xanalogs & derivatives |
650 | 0 | 4 |
_aVision Disorders _xdrug therapy |
650 | 0 | 4 |
_aVisual Acuity _xphysiology |
650 | 0 | 4 | _aVisual Field Tests |
650 | 0 | 4 |
_aVitamin B Complex _xtherapeutic use |
650 | 0 | 4 | _aYoung Adult |
700 | 1 | _aKigasawa, Kazuteru | |
700 | 1 | _aShinoda, Kei | |
700 | 1 | _aWakakura, Masato | |
700 | 1 | _aOguchi, Yoshihisa | |
773 | 0 |
_tBMC ophthalmology _gvol. 17 _gno. 1 _gp. 192 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1186/s12886-017-0583-3 _zAvailable from publisher's website |
999 |
_c27699831 _d27699831 |