| 000 | 01511 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250516055607.0 | ||
| 264 | 0 | _c20111206 | |
| 008 | 201112s 0 0 spa d | ||
| 022 | _a0535-5133 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aCammarata-Scalisi, Francisco | |
| 245 | 0 | 0 |
_a[Pearson syndrome. Case report]. _h[electronic resource] |
| 260 |
_bInvestigacion clinica _cSep 2011 |
||
| 300 |
_a261-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase, Long-Chain _xdeficiency |
| 650 | 0 | 4 |
_aAnemia, Sideroblastic _xblood |
| 650 | 0 | 4 | _aCongenital Bone Marrow Failure Syndromes |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 |
_aDiarrhea, Infantile _xetiology |
| 650 | 0 | 4 |
_aExocrine Pancreatic Insufficiency _xetiology |
| 650 | 0 | 4 | _aFatal Outcome |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypokalemia _xetiology |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aLipid Metabolism, Inborn Errors |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xblood |
| 650 | 0 | 4 | _aMuscular Diseases |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aReferral and Consultation |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aLópez-Gallardo, Ester | |
| 700 | 1 | _aEmperador, Sonia | |
| 700 | 1 | _aRuiz-Pesini, Eduardo | |
| 700 | 1 | _aDa Silva, Gloria | |
| 700 | 1 | _aCamacho, Nolis | |
| 700 | 1 | _aMontoya, Julio | |
| 773 | 0 |
_tInvestigacion clinica _gvol. 52 _gno. 3 _gp. 261-7 |
|
| 999 |
_c21187596 _d21187596 |
||