| 000 | 01531 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250514005403.0 | ||
| 264 | 0 | _c20010830 | |
| 008 | 200108s 0 0 eng d | ||
| 022 | _a0174-304X | ||
| 024 | 7 |
_a10.1055/s-2000-12943 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZafeiriou, D I | |
| 245 | 0 | 0 |
_aAtypical and variable clinical presentation of glutaric aciduria type I. _h[electronic resource] |
| 260 |
_bNeuropediatrics _cDec 2000 |
||
| 300 |
_a303-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAmino Acid Metabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 |
_aCerebral Cortex _xpathology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGlutarates _xurine |
| 650 | 0 | 4 | _aGlutaryl-CoA Dehydrogenase |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aNervous System Diseases _xetiology |
| 650 | 0 | 4 |
_aOxidoreductases _xgenetics |
| 650 | 0 | 4 | _aOxidoreductases Acting on CH-CH Group Donors |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aTwins, Monozygotic |
| 700 | 1 | _aZschocke, J | |
| 700 | 1 | _aAugoustidou-Savvopoulou, P | |
| 700 | 1 | _aMauromatis, I | |
| 700 | 1 | _aSewell, A | |
| 700 | 1 | _aKontopoulos, E | |
| 700 | 1 | _aKatzos, G | |
| 700 | 1 | _aHoffmann, G F | |
| 773 | 0 |
_tNeuropediatrics _gvol. 31 _gno. 6 _gp. 303-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1055/s-2000-12943 _zAvailable from publisher's website |
| 999 |
_c11433340 _d11433340 |
||