000 | 01858 a2200601 4500 | ||
---|---|---|---|
005 | 20250516061604.0 | ||
264 | 0 | _c20120105 | |
008 | 201201s 0 0 eng d | ||
022 | _a1526-632X | ||
024 | 7 |
_a10.1212/WNL.0b013e318237f649 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aKwon, J M | |
245 | 0 | 0 |
_aQuantifying physical decline in juvenile neuronal ceroid lipofuscinosis (Batten disease). _h[electronic resource] |
260 |
_bNeurology _cNov 2011 |
||
300 |
_a1801-7 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAnalysis of Variance |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aCross-Sectional Studies |
650 | 0 | 4 | _aPersons with Disabilities |
650 | 0 | 4 | _aDisease Progression |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMembrane Glycoproteins |
650 | 0 | 4 | _aMolecular Chaperones |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 |
_aNeuronal Ceroid-Lipofuscinoses _xdiagnosis |
650 | 0 | 4 | _aNeuropsychological Tests |
650 | 0 | 4 | _aProspective Studies |
650 | 0 | 4 | _aRegression Analysis |
650 | 0 | 4 | _aReproducibility of Results |
650 | 0 | 4 | _aYoung Adult |
700 | 1 | _aAdams, H | |
700 | 1 | _aRothberg, P G | |
700 | 1 | _aAugustine, E F | |
700 | 1 | _aMarshall, F J | |
700 | 1 | _aDeblieck, E A | |
700 | 1 | _aVierhile, A | |
700 | 1 | _aBeck, C A | |
700 | 1 | _aNewhouse, N J | |
700 | 1 | _aCialone, J | |
700 | 1 | _aLevy, E | |
700 | 1 | _aRamirez-Montealegre, D | |
700 | 1 | _aDure, L S | |
700 | 1 | _aRose, K R | |
700 | 1 | _aMink, J W | |
773 | 0 |
_tNeurology _gvol. 77 _gno. 20 _gp. 1801-7 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1212/WNL.0b013e318237f649 _zAvailable from publisher's website |
999 |
_c21245159 _d21245159 |