| 000 | 01911 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250518022717.0 | ||
| 264 | 0 | _c20200401 | |
| 008 | 202004s 0 0 eng d | ||
| 022 | _a1573-2665 | ||
| 024 | 7 |
_a10.1002/jimd.12037 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBleeker, Jeannette C | |
| 245 | 0 | 0 |
_aProposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _c01 2019 |
||
| 300 |
_a159-168 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase _xdeficiency |
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase, Long-Chain _xdeficiency |
| 650 | 0 | 4 |
_aCongenital Bone Marrow Failure Syndromes _xdrug therapy |
| 650 | 0 | 4 | _aDiet |
| 650 | 0 | 4 |
_aFatty Acids _xadministration & dosage |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aLipid Metabolism, Inborn Errors _xdrug therapy |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xdrug therapy |
| 650 | 0 | 4 |
_aMuscular Diseases _xdrug therapy |
| 650 | 0 | 4 |
_aNeonatal Screening _xmethods |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aTriglycerides _xadministration & dosage |
| 700 | 1 | _aKok, Irene L | |
| 700 | 1 | _aFerdinandusse, Sacha | |
| 700 | 1 | _ade Vries, Maaike | |
| 700 | 1 | _aDerks, Terry G J | |
| 700 | 1 | _aMulder, Margot F | |
| 700 | 1 | _aWilliams, Monique | |
| 700 | 1 | _aGozalbo, Estela Rubio | |
| 700 | 1 | _aBosch, Annet M | |
| 700 | 1 | _avan den Hurk, Dorine T | |
| 700 | 1 | _ade Sain-van der Velden, Monique G M | |
| 700 | 1 | _aWaterham, Hans R | |
| 700 | 1 | _aWijburg, Frits A | |
| 700 | 1 | _aVisser, Gepke | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 42 _gno. 1 _gp. 159-168 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/jimd.12037 _zAvailable from publisher's website |
| 999 |
_c29349539 _d29349539 |
||