| 000 | 01702 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250514200814.0 | ||
| 264 | 0 | _c20040914 | |
| 008 | 200409s 0 0 eng d | ||
| 022 | _a1549-4713 | ||
| 024 | 7 |
_a10.1016/j.ophtha.2004.03.026 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSanders, Donald R | |
| 245 | 0 | 0 |
_aUnited States Food and Drug Administration clinical trial of the Implantable Collamer Lens (ICL) for moderate to high myopia: three-year follow-up. _h[electronic resource] |
| 260 |
_bOphthalmology _cSep 2004 |
||
| 300 |
_a1683-92 p. _bdigital |
||
| 500 | _aPublication Type: Clinical Trial; Controlled Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAnterior Chamber _xsurgery |
| 650 | 0 | 4 | _aCell Count |
| 650 | 0 | 4 | _aContact Lenses |
| 650 | 0 | 4 |
_aContrast Sensitivity _xphysiology |
| 650 | 0 | 4 |
_aEndothelium, Corneal _xpathology |
| 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 |
_aMyopia _xphysiopathology |
| 650 | 0 | 4 | _aPatient Satisfaction |
| 650 | 0 | 4 | _aPostoperative Complications |
| 650 | 0 | 4 | _aProspective Studies |
| 650 | 0 | 4 | _aProsthesis Design |
| 650 | 0 | 4 | _aProsthesis Implantation |
| 650 | 0 | 4 | _aSafety |
| 650 | 0 | 4 | _aTreatment Outcome |
| 650 | 0 | 4 | _aUnited States |
| 650 | 0 | 4 | _aUnited States Food and Drug Administration |
| 650 | 0 | 4 |
_aVisual Acuity _xphysiology |
| 700 | 1 | _aDoney, Kimberley | |
| 700 | 1 | _aPoco, Monica | |
| 773 | 0 |
_tOphthalmology _gvol. 111 _gno. 9 _gp. 1683-92 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ophtha.2004.03.026 _zAvailable from publisher's website |
| 999 |
_c15045946 _d15045946 |
||