| 000 | 01675 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250515151836.0 | ||
| 264 | 0 | _c20081231 | |
| 008 | 200812s 0 0 hun d | ||
| 022 | _a0019-1442 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNagy, Andrea | |
| 245 | 0 | 0 |
_a[Convulsions in neonatal period and infancy with rare etiology (neurogenetic disease)]. _h[electronic resource] |
| 260 |
_bIdeggyogyaszati szemle _cNov 2008 |
||
| 300 |
_a417-22 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAmino Acid Metabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 |
_aCerebral Hemorrhage _xcomplications |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aElectroencephalography |
| 650 | 0 | 4 |
_aEpilepsy, Benign Neonatal _xdiagnostic imaging |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypoxia _xcomplications |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aLeigh Disease _xcomplications |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 |
_aMetabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 |
_aMitochondrial Proteins _xgenetics |
| 650 | 0 | 4 | _aMolecular Chaperones |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aUltrasonography, Doppler |
| 700 | 1 | _aSzever, Zsuzsa | |
| 700 | 1 | _aKormos, Zsuzsa | |
| 700 | 1 | _aSzékely, Emoke | |
| 700 | 1 | _aTóth, Edit | |
| 700 | 1 | _aSmidéliusz, Lajos | |
| 700 | 1 | _aHorváth, Rita | |
| 700 | 1 | _aKarcagi, Vera | |
| 700 | 1 | _aSchuler, Agnes | |
| 700 | 1 | _aJávorszky, Eszter | |
| 773 | 0 |
_tIdeggyogyaszati szemle _gvol. 61 _gno. 11-12 _gp. 417-22 |
|
| 999 |
_c18523260 _d18523260 |
||