000 | 01788 a2200541 4500 | ||
---|---|---|---|
005 | 20250515131608.0 | ||
264 | 0 | _c20081103 | |
008 | 200811s 0 0 eng d | ||
022 | _a1096-7206 | ||
024 | 7 |
_a10.1016/j.ymgme.2008.06.007 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aCosson, M A | |
245 | 0 | 0 |
_aLiver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria. _h[electronic resource] |
260 |
_bMolecular genetics and metabolism _c |
||
300 |
_a107-9 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aCells, Cultured |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aElectron Transport |
650 | 0 | 4 | _aFatal Outcome |
650 | 0 | 4 |
_aFibroblasts _xenzymology |
650 | 0 | 4 | _aFollow-Up Studies |
650 | 0 | 4 |
_aHepatoblastoma _xenzymology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aImmunosuppressive Agents _xadverse effects |
650 | 0 | 4 |
_aKidney _xenzymology |
650 | 0 | 4 |
_aKidney Transplantation _xadverse effects |
650 | 0 | 4 |
_aLipid Metabolism, Inborn Errors _xcomplications |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMethylmalonic Acid _xmetabolism |
650 | 0 | 4 |
_aMethylmalonyl-CoA Mutase _xgenetics |
650 | 0 | 4 | _aMutation |
700 | 1 | _aTouati, G | |
700 | 1 | _aLacaille, F | |
700 | 1 | _aValayannnopoulos, V | |
700 | 1 | _aGuyot, C | |
700 | 1 | _aGuest, G | |
700 | 1 | _aVerkarre, V | |
700 | 1 | _aChrétien, D | |
700 | 1 | _aRabier, D | |
700 | 1 | _aMunnich, A | |
700 | 1 | _aBenoist, J F | |
700 | 1 | _ade Keyzer, Y | |
700 | 1 | _aNiaudet, P | |
700 | 1 | _ade Lonlay, P | |
773 | 0 |
_tMolecular genetics and metabolism _gvol. 95 _gno. 1-2 _gp. 107-9 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ymgme.2008.06.007 _zAvailable from publisher's website |
999 |
_c18151431 _d18151431 |