000 | 01676 a2200481 4500 | ||
---|---|---|---|
005 | 20250515042159.0 | ||
264 | 0 | _c20061204 | |
008 | 200612s 0 0 eng d | ||
022 | _a0887-8994 | ||
024 | 7 |
_a10.1016/j.pediatrneurol.2006.05.007 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aOglesbee, Devin | |
245 | 0 | 0 |
_aNormal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis. _h[electronic resource] |
260 |
_bPediatric neurology _cOct 2006 |
||
300 |
_a289-92 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 |
_aAcidosis, Lactic _xdiagnosis |
650 | 0 | 4 | _aAtrophy |
650 | 0 | 4 | _aBiopsy |
650 | 0 | 4 | _aBlotting, Western |
650 | 0 | 4 |
_aCarnitine _xanalogs & derivatives |
650 | 0 | 4 |
_aCentral Nervous System Cysts _xdiagnosis |
650 | 0 | 4 |
_aCerebral Ventricles _xpathology |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 | _aDiagnosis, Differential |
650 | 0 | 4 |
_aElectron Transport Complex I _xdeficiency |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFibroblasts _xenzymology |
650 | 0 | 4 |
_aFrontal Lobe _xpathology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMagnetic Resonance Imaging |
650 | 0 | 4 |
_aMitochondrial Diseases _xdiagnosis |
650 | 0 | 4 |
_aMuscle, Skeletal _xenzymology |
650 | 0 | 4 |
_aNerve Fibers, Myelinated _xpathology |
650 | 0 | 4 | _aPoint Mutation |
700 | 1 | _aFreedenberg, Debra | |
700 | 1 | _aKramer, Karen A | |
700 | 1 | _aAnderson, Bambi D | |
700 | 1 | _aHahn, Si Houn | |
773 | 0 |
_tPediatric neurology _gvol. 35 _gno. 4 _gp. 289-92 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.pediatrneurol.2006.05.007 _zAvailable from publisher's website |
999 |
_c16574880 _d16574880 |