| 000 | 01543 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250516114540.0 | ||
| 264 | 0 | _c20140519 | |
| 008 | 201405s 0 0 eng d | ||
| 022 | _a1573-2665 | ||
| 024 | 7 |
_a10.1007/s10545-012-9542-6 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBaruteau, Julien | |
| 245 | 0 | 0 |
_aClinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cSep 2013 |
||
| 300 |
_a795-803 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Multicenter Study | ||
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase _xdeficiency |
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase, Long-Chain _xdeficiency |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aFatty Acids _xmetabolism |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aLipid Metabolism, Inborn Errors _xdiagnosis |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondria _xmetabolism |
| 650 | 0 | 4 | _aOxidation-Reduction |
| 650 | 0 | 4 | _aRetrospective Studies |
| 700 | 1 | _aSachs, Philippe | |
| 700 | 1 | _aBroué, Pierre | |
| 700 | 1 | _aBrivet, Michèle | |
| 700 | 1 | _aAbdoul, Hendy | |
| 700 | 1 | _aVianey-Saban, Christine | |
| 700 | 1 | _aOgier de Baulny, Hélène | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 36 _gno. 5 _gp. 795-803 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10545-012-9542-6 _zAvailable from publisher's website |
| 999 |
_c22173472 _d22173472 |
||