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